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Harvey Mohrenweiser

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Roy E Shore; Anne Zeleniuch-Jacquotte; Diane Currie; Harvey W Mohrenweiser; Yelena Afanasyeva; Karen L Koenig; Alan A Arslan; Paolo Toniolo; Isaac Wirgin
Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk.
Su-Jun Lee; Lalith Perera; Sherry J Coulter; Harvey W Mohrenweiser; Anton Jetten; Joyce A Goldstein
The discovery of new coding alleles of human CYP26A1 that are potentially defective in the metabolism of all-trans retinoic acid and their assessment in a recombinant cDNA expression system.
Harvey W Mohrenweiser
Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes.

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2008: Roy E Shore; Anne Zeleniuch-Jacquotte; Diane Currie; Harvey W Mohrenweiser; Yelena Afanasyeva; Karen L Koenig; Alan A Arslan; Paolo Toniolo; Isaac Wirgin
Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk.
International journal of cancer. Journal international du cancer 2008;122(9):2101-5.
2007: Su-Jun Lee; Lalith Perera; Sherry J Coulter; Harvey W Mohrenweiser; Anton Jetten; Joyce A Goldstein
The discovery of new coding alleles of human CYP26A1 that are potentially defective in the metabolism of all-trans retinoic acid and their assessment in a recombinant cDNA expression system.
Pharmacogenetics and genomics 2007;17(3):169-80.
2007: Harvey W Mohrenweiser
Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes.
Mutation research 2007;616(1-2):221-6.
2007: Irene M Jones; Cynthia B Thomas; Tina Xi; Harvey W Mohrenweiser; David O Nelson
Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes.
Mutation research 2007;616(1-2):213-20.
2007: Craig R Lee; Leping Li; Harvey W Mohrenweiser; Robert M Petrovich; Douglas A Bell; Frank G Bottone; Molly E Cook; Thomas E Eling; Joseph M Krahn; Darryl C Zeldin
Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1).
Pharmacogenetics and genomics 2007;17(2):145-60.
2007: Ellen T Chang; Alison J Canchola; Valerie S Lee; Christina Clarke; David M Purdie; Peggy Reynolds; Leslie Bernstein; Daniel O Stram; Hoda Anton-Culver; Dennis Deapen; Harvey W Mohrenweiser; David Peel; Richard Pinder; Ronald K Ross; Dee W West; William Wright; Argyrios Ziogas; Pamela L Horn-Ross
Wine and other alcohol consumption and risk of ovarian cancer in the California Teachers Study cohort.
Cancer causes & control : CCC 2007;18(1):91-103.
2006: John M Hinz; Peter B Nham; N Alice Yamada; Robert S Tebbs; Edmund P Salazar; Angela K Hinz; Harvey W Mohrenweiser; Irene M Jones; Larry H Thompson
Four human FANCG polymorphic variants show normal biological function in hamster CHO cells.
Mutation research 2006;602(1-2):34-42.
2006: Robert C Millikan; Amanda J Hummer; Colin B Begg; Jon Player; Allan René de Cotret; Scott Winkel; Harvey W Mohrenweiser; Nancy E Thomas; Bruce Armstrong; Anne Kricker; Loraine D Marrett; Stephen B Gruber; Hoda Anton Culver; Roberto Zanetti; Richard P Gallagher; Terence Dwyer; Timothy R Rebbeck; Klaus J Busam; Lynn From; Urvi Mujumdar; Marianne Berwick
Polymorphisms in nucleotide excision repair genes and risk of multiple primary melanoma: the Genes Environment and Melanoma Study.
Carcinogenesis 2006;27(3):610-8.
2006: Ana Virginia Dutra; Hsiu-Fen Lin; Suh-Hang Hank Juo; Harvey W Mohrenweiser; Souvik Sen; Raji P Grewal
Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke.
BMC medical genetics 2006;7():78.
2005: Kelly Bleasby; Laura A Hall; Jennifer Perry; Harvey W Mohrenweiser; John B Pritchard
Functional consequences of single nucleotide polymorphisms in the human organic anion transporter hOAT1 (SLC22A6).
The Journal of pharmacology and experimental therapeutics 2005;314(2):923-31.
2005: Irene M Jones; Cynthia B Thomas; Tina Xi; David O Nelson; Harvey W Mohrenweiser
The genetic basis for variation in radiation sensitivity in the general population.
Radiation research 2005;163(6):700-1.
2005: Sarah F Marshall; Leslie Bernstein; Hoda Anton-Culver; Dennis Deapen; Pamela L Horn-Ross; Harvey W Mohrenweiser; David Peel; Richard Pinder; David M Purdie; Peggy Reynolds; Daniel O Stram; Dee West; William E Wright; Argyrios Ziogas; Ronald K Ross
Nonsteroidal anti-inflammatory drug use and breast cancer risk by stage and hormone receptor status.
Journal of the National Cancer Institute 2005;97(11):805-12.
2004: Joyce Blaisdell; Lucia F Jorge-Nebert; Sherry J Coulter; Stephen S Ferguson; Su-Jun Lee; Brian Chanas; Tina Xi; Harvey W Mohrenweiser; Burhan I Ghanayem; Joyce A Goldstein
Discovery of new potentially defective alleles of human CYP2C9.
Pharmacogenetics 2004;14(8):527-37.
2004: Tina Xi; Irene M Jones; Harvey W Mohrenweiser
Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function.
Genomics 2004;83(6):970-9.
2004: Harvey W Mohrenweiser
Genetic variation and exposure related risk estimation: will toxicology enter a new era? DNA repair and cancer as a paradigm.
Toxicologic pathology 2004;32 Suppl 1():136-45.
2003: Jiali Han; Susan E Hankinson; Immaculata DeVivo; Donna Spiegelman; Rulla M Tamimi; Harvey W Mohrenweiser; GRaham Colditz; David J Hunter
A prospective study of XRCC1 haplotypes and their interaction with plasma carotenoids on breast cancer risk.
Cancer research 2003;63(23):8536-41.
2003: Tasha R Smith; Edward A Levine; Nancy D Perrier; Mark Steven Miller; Rita I Freimanis; Kurt Lohman; L Douglas Case; Jianfeng Xu; Harvey W Mohrenweiser; Jennifer Hu
DNA-repair genetic polymorphisms and breast cancer risk.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2003;12(11 Pt 1):1200-4.
2003: Su-Jun Lee; Khawja A Usmani; Brian Chanas; Burhan I Ghanayem; Tina Xi; Ernest Hodgson; Harvey W Mohrenweiser; Joyce A Goldstein
Genetic findings and functional studies of human CYP3A5 single nucleotide polymorphisms in different ethnic groups.
Pharmacogenetics 2003;13(8):461-72.
2003: Beata D Przybyla-Zawislak; Punit K Srivastava; Johana Vazquez-Matias; Harvey W Mohrenweiser; Joseph E Maxwell; Bruce D Hammock; J Alyce Bradbury; Ahmed E Enayetallah; Darryl C Zeldin; David F Grant
Polymorphisms in human soluble epoxide hydrolase.
Molecular pharmacology 2003;64(2):482-90.
2003: Harvey W Mohrenweiser; David Michael Wilson; Irene M Jones
Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes.
Mutation research 2003;526(1-2):93-125.
2003: Tasha R Smith; Mark Steven Miller; Kurt Lohman; Ethan M Lange; L Douglas Case; Harvey W Mohrenweiser; Jennifer Hu
Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer.
Cancer letters 2003;190(2):183-90.
2003: Perry Blackshear; Ruth S Phillips; Johana Vazquez-Matias; Harvey W Mohrenweiser
Polymorphisms in the genes encoding members of the tristetraprolin family of human tandem CCCH zinc finger proteins.
Progress in nucleic acid research and molecular biology 2003;75():43-68.
2002: Joyce Blaisdell; Harvey W Mohrenweiser; Jonathan Jackson; Stephen Ferguson; Sherry J Coulter; Brian Chanas; Tina Xi; Burhan I Ghanayem; Joyce A Goldstein
Identification and functional characterization of new potentially defective alleles of human CYP2C19.
Pharmacogenetics 2002;12(9):703-11.
2002: Jennifer Hu; Harvey W Mohrenweiser; D A Bell; Steven A Leadon; Mark Steven Miller
Symposium overview: genetic polymorphisms in DNA repair and cancer risk.
Toxicology and applied pharmacology 2002;185(1):64-73.
2002: Harvey W Mohrenweiser; Tina Xi; Johana Vázquez-Matías; Irene M Jones
Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2002;11(10 Pt 1):1054-64.
2002: Lorraine M King; Jixiang Ma; Supawon Srettabunjong; Joan Graves; J Alyce Bradbury; Leping Li; Martin Spiecker; James K Liao; Harvey W Mohrenweiser; Darryl C Zeldin
Cloning of CYP2J2 gene and identification of functional polymorphisms.
Molecular pharmacology 2002;61(4):840-52.
2002: Yawei Qiao; Margaret R Spitz; Hongbing Shen; Zhaozheng Guo; Sanjay Shete; Mohammad Hedayati; Lawrence Grossman; Harvey W Mohrenweiser; Qingyi Wei
Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes.
Carcinogenesis 2002;23(2):295-9.
2001: D Dai; J Tang; R Rose; Ernest Hodgson; Rachelle J Bienstock; Harvey W Mohrenweiser; Joyce A Goldstein
Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos.
The Journal of pharmacology and experimental therapeutics 2001;299(3):825-31.
2001: Jennifer Hu; Tasha R Smith; Mark Steven Miller; Harvey W Mohrenweiser; A Golden; L Douglas Case
Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity.
Carcinogenesis 2001;22(6):917-22.
2001: M C Miller; Harvey W Mohrenweiser; Douglas A Bell
Genetic variability in susceptibility and response to toxicants.
Toxicology letters 2001;120(1-3):269-80.
2001: EJ Duell; Robert C Millikan; Gary S Pittman; Scott Winkel; R M Lunn; Chiu-Kit Tse; Allison Eaton; Harvey W Mohrenweiser; Beth Newman; Douglas A Bell
Polymorphisms in the DNA repair gene XRCC1 and breast cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2001;10(3):217-22.
2001: Margaret R Spitz; Xifeng Wu; Yunfei Wang; Li-E Wang; Sanjay Shete; Christopher I Amos; Zhaozheng Guo; L Lei; Harvey W Mohrenweiser; Qingyi Wei
Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients.
Cancer research 2001;61(4):1354-7.
2000: Harvey W Mohrenweiser; Irene M Jones
Uncertainty of response to ionizing radiation due to genotype: potential role for variation in DNA repair genes.
Radiation research 2000;154(6):722-3;discussion 723-4.
2000: Masood Z Hadi; Matthew A Coleman; Krzysztof Fidelis; Harvey W Mohrenweiser; David Michael Wilson
Functional characterization of Ape1 variants identified in the human population.
Nucleic acids research 2000;28(20):3871-9.
2000: K Chin; Xiaobing Yu; Bojana B Beleslin-Cokic; C Liu; K Shen; Harvey W Mohrenweiser; Constance Tom Noguchi
Production and processing of erythropoietin receptor transcripts in brain.
Brain research. Molecular brain research 2000;81(1-2):29-42.
2000: JS Smith; Issei Tachibana; HK Lee; Junqi Qian; U Pohl; Harvey W Mohrenweiser; Thomas J Borell; SM Hosek; Cheryl L Soderberg; A von Deimling; Arie Perry; Bernd W Scheithauer; David N Louis; Robert B Jenkins
Mapping of the chromosome 19 q-arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers.
Genes, chromosomes & cancer 2000;29(1):16-25.
2000: Matthew A Coleman; Jonathan Eisen; Harvey W Mohrenweiser
Cloning and characterization of HARP/SMARCAL1: a prokaryotic HepA-related SNF2 helicase protein from human and mouse.
Genomics 2000;65(3):274-82.
2000: JS Smith; Issei Tachibana; U Pohl; HK Lee; U Thanarajasingam; B P Portier; K Ueki; S Ramaswamy; SJ Billings; Harvey W Mohrenweiser; David N Louis; Robert B Jenkins
A transcript map of the chromosome 19q-arm glioma tumor suppressor region.
Genomics 2000;64(1):44-50.
2000: U Pohl; JS Smith; Issei Tachibana; K Ueki; HK Lee; S Ramaswamy; Qiang Wu; Harvey W Mohrenweiser; Robert B Jenkins; David N Louis
EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins.
Genomics 2000;63(2):255-62.
1999: Serenella Servidei; Francesca Capon; antonella spinazzola; Massimiliano Mirabella; Sabrina Semprini; G de Rosa; Massimo Gennarelli; Federica Sangiuolo; Enzo Ricci; Harvey W Mohrenweiser; Bruno Dallapiccola; Pietro Tonali; Giuseppe Novelli
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.
Neurology 1999;53(4):830-7.
1998: C Her; Thomas C Wood; Evan E Eichler; Harvey W Mohrenweiser; Louis S Ramagli; Michael J Siciliano; Richard M Weinshilboum
Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene.
Genomics 1998;53(3):284-95.
1998: Evan E Eichler; S M Hoffman; A A Adamson; LA Gordon; PM McCready; Jane Lamerdin; Harvey W Mohrenweiser
Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12.
Genome research 1998;8(8):791-808.
1998: S Ghanshani; M Coleman; P Gustavsson; A C Wu; J Jay Gargus; George A Gutman; N Dahl; Harvey W Mohrenweiser; K George Chandy
Human calcium-activated potassium channel gene KCNN4 maps to chromosome 19q13.2 in the region deleted in diamond-blackfan anemia.
Genomics 1998;51(1):160-1.
1998: Harvey W Mohrenweiser; Irene M Jones
Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation?
Mutation research 1998;400(1-2):15-24.
1998: Katalin Kalman; A Nguyen; Julie Tseng-Crank; I D Dukes; G Chandy; C M Hustad; N G Copeland; N A Jenkins; Harvey W Mohrenweiser; B Brandriff; Michael D Cahalan; George A Gutman; K George Chandy
Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7.
The Journal of biological chemistry 1998;273(10):5851-7.
1998: MR Shen; I M Jones; Harvey W Mohrenweiser
Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans.
Cancer research 1998;58(4):604-8.
1998: MR Shen; Malgorzata Z Zdzienicka; Harvey W Mohrenweiser; Larry H Thompson; Michael P Thelen
Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair.
Nucleic acids research 1998;26(4):1032-7.
1998: Harvey W Mohrenweiser; S Tsujimoto; Laurie Gordon; Anne S Olsen
Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19.
Genomics 1998;47(2):153-62.
1997: Nicolai Wagtmann; SC Rojo; Evan E Eichler; Harvey W Mohrenweiser; Eric O Long
A new human gene complex encoding the killer cell inhibitory receptors and related monocyte/macrophage receptors.
Current biology : CB 1997;7(8):615-8.
1997: S M Hoffman; K S Lai; J Tomfohrde; A Bowcock; LA Gordon; Harvey W Mohrenweiser
JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors.
Genomics 1997;43(1):109-11.
1997: Evan E Eichler; M L Budarf; M Rocchi; LL Deaven; Norman A Doggett; A Baldini; D L Nelson; Harvey W Mohrenweiser
Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.
Human molecular genetics 1997;6(7):991-1002.
1997: K Ueki; S Ramaswamy; SJ Billings; Harvey W Mohrenweiser; David N Louis
ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3.
Neurogenetics 1997;1(1):31-6.
1997: K Ueki; S Ramaswamy; SJ Billings; Harvey W Mohrenweiser; David N Louis
Chromosomal localization to 19q13.3, partial genomic structure and 5' cDNA sequence of the human symplekin gene.
Somatic cell and molecular genetics 1997;23(3):229-31.
1997: AM Nystuen; H Costeff; O N Elpeleg; N Apter; B Bonné-Tamir; Harvey W Mohrenweiser; Neena B Haider; Edwin M Stone; Val C Sheffield
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene.
Human molecular genetics 1997;6(4):563-9.
1996: J E Rosenberg; D K Lisle; J A Burwick; K Ueki; A von Deimling; Harvey W Mohrenweiser; David N Louis
Refined deletion mapping of the chromosome 19q glioma tumor suppressor gene to the D19S412-STD interval.
Oncogene 1996;13(11):2483-5.
1996: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Ronald van Eijk; P J Oefner; S M Hoffman; Jane Lamerdin; Harvey W Mohrenweiser; D E Bulman; M Ferrari; Joost Haan; Dick Lindhout; Gert-Jan B van Ommen; M H Hofker; Michel D Ferrari; Rune R Frants
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Cell 1996;87(3):543-52.
1996: Lisa Stubbs; Ethan Carver; M E Shannon; Joomyeong Kim; J Geisler; E E Generoso; B G Stanford; W C Dunn; Harvey W Mohrenweiser; W Zimmermann; S M Watt; L K Ashworth
Detailed comparative map of human chromosome 19q and related regions of the mouse genome.
Genomics 1996;35(3):499-508.
1996: Lena Stenson Holst; Dominique Langin; Hindrik Mulder; H Laurell; jacques Grober; A Bergh; Harvey W Mohrenweiser; G Edgren; Cecilia Holm
Molecular cloning, genomic organization, and expression of a testicular isoform of hormone-sensitive lipase.
Genomics 1996;35(3):441-7.
1996: D Chou; T Miyashita; Harvey W Mohrenweiser; K Ueki; K Kastury; Teresa Druck; A von Deimling; Kay Huebner; J C Reed; David N Louis
The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas.
Cancer genetics and cytogenetics 1996;88(2):136-40.
1996: S M Hoffman; R Hromas; C Amemiya; Harvey W Mohrenweiser
The location of MZF-1 at the telomere of human chromosome 19q makes it vulnerable to degeneration in aging cells.
Leukemia research 1996;20(3):281-3.
1996: M Watanabe; B C Zingg; Harvey W Mohrenweiser
Molecular analysis of a series of alleles in humans with reduced activity at the triosephosphate isomerase locus.
American journal of human genetics 1996;58(2):308-16.
1996: G C Shonnard; Nicholas Vincent Hud; Harvey W Mohrenweiser
Arginine to tryptophan substitution in the active site of a human lactate dehydrogenase variant--LDHB GUA1: postulated effects on subunit structure and catalysis.
Biochimica et biophysica acta 1996;1315(1):9-14.
1996: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Ronald van Eijk; Harvey W Mohrenweiser; M Litt; M H Hofker; Joost Haan; Michel D Ferrari; Rune R Frants
A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.
European journal of human genetics : EJHG 1996;4(6):321-8.
1996: Harvey W Mohrenweiser; A Olsen; A Archibald; C Beattie; Margit Burmeister; Jane Lamerdin; GG Lennon; E Stewart; Lisa Stubbs; J L Weber; K Johnson
Report an abstracts of the third international workshop on human chromosome 19 mapping 1996.
Cytogenetics and cell genetics 1996;74(3):161-86.
1995: S M Hoffman; Pedro Fernandez-Salguero; F J Gonzalez; Harvey W Mohrenweiser
Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19.
Journal of molecular evolution 1995;41(6):894-900.
1995: L K Ashworth; M A Batzer; B Brandriff; Elbert Branscomb; P de Jong; E Garcia; J A Garnes; L A Gordon; Jane Lamerdin; GG Lennon; Harvey W Mohrenweiser; Anne S Olsen; T Slezak; A V Carrano
An integrated metric physical map of human chromosome 19.
Nature genetics 1995;11(4):422-7.
1995: L A Gordon; A Bergmann; M Christensen; L Danganan; D A Lee; L K Ashworth; David O Nelson; Anne S Olsen; Harvey W Mohrenweiser; A V Carrano
A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q.
Genomics 1995;30(2):187-94.
1995: W H Yong; K Ueki; D Chou; S A Reeves; A von Deimling; James Gusella; Harvey W Mohrenweiser; AJ Buckler; David N Louis
Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3.
Genomics 1995;29(2):533-6.
1995: Pedro Fernandez-Salguero; S M Hoffman; S Cholerton; Harvey W Mohrenweiser; H Raunio; Arja Rautio; Olavi Pelkonen; J D Huang; William Evans; Jeffrey Idle
A genetic polymorphism in coumarin 7-hydroxylation: sequence of the human CYP2A genes and identification of variant CYP2A6 alleles.
American journal of human genetics 1995;57(3):651-60.
1995: W H Yong; D Chou; K Ueki; G R Harsh; A von Deimling; James Gusella; Harvey W Mohrenweiser; David N Louis
Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112.
Journal of neuropathology and experimental neurology 1995;54(5):622-6.
1995: H Laurell; jacques Grober; Lena Stenson Holst; Cecilia Holm; Harvey W Mohrenweiser; Dominique Langin
The hormone-sensitive lipase (LIPE) gene located on chromosome 19q13.1-->13.2 is not duplicated on 19p13.3.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 1995;19(8):590-2.
1995: Michael D Briggs; S M Hoffman; Lily M King; Anne S Olsen; Harvey W Mohrenweiser; Jules G Leroy; Geert R Mortier; David L Rimoin; Ralph S Lachman; E S Gaines
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene.
Nature genetics 1995;10(3):330-6.
1995: B C Zingg; W Pretsch; Harvey W Mohrenweiser
Molecular analysis of four ENU induced triosephosphate isomerase null mutants in Mus musculus.
Mutation research 1995;328(2):163-73.
1995: Harvey W Mohrenweiser; B Zingg
Mosaicism: the embryo as a target for induction of mutations leading to cancer and genetic disease.
Environmental and molecular mutagenesis 1995;25 Suppl 26():21-9.
1995: DM Otterness; Harvey W Mohrenweiser; B F Brandriff; Richard M Weinshilboum
Dehydroepiandrosterone sulfotransferase gene (STD): localization to human chromosome band 19q13.3.
Cytogenetics and cell genetics 1995;70(1-2):45-7.
1995: Roy Levitt; Z Liu; N Nouri; Deborah A Meyers; B Brandriff; Harvey W Mohrenweiser
Mapping of the gene for hormone sensitive lipase (LIPE) to chromosome 19q13.1-->q13.2.
Cytogenetics and cell genetics 1995;69(3-4):211-4.
1995: Harvey W Mohrenweiser; S Tsujimoto; K Tynan; Jane Lamerdin; A V Carrano
Unique sequence STSs for 21 cytogenetically mapped loci on human chromosome 19.
Cytogenetics and cell genetics 1995;71(1):58-61.
1994: B F Brandriff; L A Gordon; A Fertitta; Anne S Olsen; M Christensen; L K Ashworth; David O Nelson; A V Carrano; Harvey W Mohrenweiser
Human chromosome 19p: a fluorescence in situ hybridization map with genomic distance estimates for 79 intervals spanning 20 Mb.
Genomics 1994;23(3):582-91.
1994: M P Rubio; K M Correa; K Ueki; Harvey W Mohrenweiser; James Gusella; A von Deimling; David N Louis
The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC.
Cancer research 1994;54(17):4760-3.
1994: S Hashimoto; Harvey W Mohrenweiser; Peter K Gregersen; Nicholas Chiorazzi
Chromosomal localization, genomic structure, and allelic polymorphism of the human CD79 alpha (Ig-alpha/mb-1) gene.
Immunogenetics 1994;40(4):287-95.
1994: Bryn A Bridges; J Cole; J Favor; B W Glickman; Harvey W Mohrenweiser; K Sankaranarayanan; T R Skopek
International Commission for Protection Against Environmental Mutagens and Carcinogens. Spontaneous mutation and its place in risk assessment for chemical mutagens. Report of an ICPEMC Committee.
Mutation research 1994;304(1):3-11.
1994: Harvey W Mohrenweiser
International Commission for Protection Against Environmental Mutagens and Carcinogens. Working paper no. 5. Impact of the molecular spectrum of mutational lesions on estimates of germinal gene-mutation rates.
Mutation research 1994;304(1):119-37.
1993: Danielle Malo; Philippe Gros; A Bergmann; Barbara J Trask; Harvey W Mohrenweiser; Victor A Canfield; Robert Levenson
Genes encoding the H,K-ATPase alpha and Na,K-ATPase alpha 3 subunits are linked on mouse chromosome 7 and human chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(11):644-9.
1993: K Tynan; S M Hoffman; S Tsujimoto; B Brandriff; L Gordon; A V Carrano; Harvey W Mohrenweiser
Organization of the multiple polymorphic sites of the D19S11 locus within a 650-kb cosmid contig.
Genomics 1993;17(2):316-23.
1993: Barbara J Trask; A Fertitta; M Christensen; J Youngblom; A Bergmann; Alex Copeland; P de Jong; Harvey W Mohrenweiser; A Olsen; A Carrano
Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers.
Genomics 1993;15(1):133-45.
1992: P Noguiez; Deborah E Barnes; Harvey W Mohrenweiser; Tomas Lindahl
Structure of the human DNA ligase I gene.
Nucleic acids research 1992;20(15):3845-50.
1992: K Tynan; A Olsen; Barbara J Trask; P de Jong; J Thompson; W Zimmermann; A Carrano; Harvey W Mohrenweiser
Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19.
Nucleic acids research 1992;20(7):1629-36.
1992: B F Brandriff; L A Gordon; K T Tynan; Anne S Olsen; Harvey W Mohrenweiser; A Fertitta; A V Carrano; Barbara J Trask
Order and genomic distances among members of the carcinoembryonic antigen (CEA) gene family determined by fluorescence in situ hybridization.
Genomics 1992;12(4):773-9.
1992: B A Perry; Harvey W Mohrenweiser
Human triosephosphate isomerase: substitution of Arg for Gly at position 122 in a thermolabile electromorph variant, TPI-Manchester.
Human genetics 1992;88(6):634-8.
1992: Deborah E Barnes; K Kodama; K Tynan; B J Trask; M Christensen; P J De Jong; Nigel K Spurr; Tomas Lindahl; Harvey W Mohrenweiser
Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3.
Genomics 1992;12(1):164-6.
1990: Dora Papadopoulo; Christel Guillouf; Harvey W Mohrenweiser; Ethel Moustacchi
Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(21):8383-7.
1990: Richard A Spritz; K Strunk; C S Surowy; Harvey W Mohrenweiser
Human U1-70K ribonucleoprotein antigen gene: organization, nucleotide sequence, and mapping to locus 19q13.3.
Genomics 1990;8(2):371-9.
1990: Harvey W Mohrenweiser; Irene M Jones
Review of the molecular characteristics of gene mutations of the germline and somatic cells of the human.
Mutation research 1990;231(1):87-108.
1990: R Barrantes; P E Smouse; Harvey W Mohrenweiser; H Gershowitz; J Azofeifa; T D Arias; James V Neel
Microevolution in lower Central America: genetic characterization of the Chibcha-speaking groups of Costa Rica and Panama, and a consensus taxonomy based on genetic and linguistic affinity.
American journal of human genetics 1990;46(1):63-84.
1989: R E Little; Harvey W Mohrenweiser; E Walters
Erythrocyte acid phosphatase phenotype and gestational length: no relationship in a sample of 3001 births.
Early human development 1989;20(2):151-4.
1989: S E Old; L E Landa; Harvey W Mohrenweiser
Hominoid triosephosphate isomerase: regulation of expression of the proliferation specific isozyme.
Molecular and cellular biochemistry 1989;89(1):73-85.
1989: Harvey W Mohrenweiser; R D Larsen; James V Neel
Development of molecular approaches to estimating germinal mutation rates. I. Detection of insertion/deletion/rearrangement variants in the human genome.
Mutation research 1989;212(2):241-52.
1989: Harvey W Mohrenweiser; A V Carrano; A Fertitta; B Perry; Larry H Thompson; James Tucker; C A Weber
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19.
Cytogenetics and cell genetics 1989;52(1-2):11-4.
1988: S E Old; Harvey W Mohrenweiser
Nucleotide sequence of the triosephosphate isomerase gene from Macaca mulatta.
Nucleic acids research 1988;16(18):9055.
1988: James V Neel; Harvey W Mohrenweiser; H Gershowitz
A pilot study of the use of placental cord blood samples in monitoring for mutational events.
Mutation research 1988;204(3):365-77.
1987: Harvey W Mohrenweiser
Functional hemizygosity in the human genome: direct estimate from twelve erythrocyte enzyme loci.
Human genetics 1987;77(3):241-5.
1987: Harvey W Mohrenweiser; K H Wurzinger; James V Neel
Frequency and distribution of rare electrophoretic mobility variants in a population of human newborns in Ann Arbor, Michigan.
Annals of human genetics 1987;51(Pt 4):303-16.
1987: Harvey W Mohrenweiser; P T Wade; K H Wurzinger
Characterization of a series of electrophoretic and enzyme activity variants of human glucose-phosphate isomerase.
Human genetics 1987;75(1):28-31.
1986: R S Decker; Harvey W Mohrenweiser
Hominoid triosephosphate isomerase: characterization of the major cell proliferation specific isozyme.
Molecular and cellular biochemistry 1986;71(1):31-44.
1986: J V Neel; Harvey W Mohrenweiser; E D Rothman; J M Naidu
A revised indirect estimate of mutation rates in Amerindians.
American journal of human genetics 1986;38(5):649-66.
1986: J C Long; J M Naidu; Harvey W Mohrenweiser; H Gershowitz; P L Johnson; J W Wood; P E Smouse
Genetic characterization of Gainj- and Kalam-speaking peoples of Papua New Guinea.
American journal of physical anthropology 1986;70(1):75-96.
1986: Francisco M Salzano; H Gershowitz; Harvey W Mohrenweiser; James V Neel; P E Smouse; M A Mestriner; Tania A Weimer; Maria Helena L P Franco; A L Simões; J Constans
Gene flow across tribal barriers and its effect among the Amazonian Içana river Indians.
American journal of physical anthropology 1986;69(1):3-14.
1985: R S Decker; Harvey W Mohrenweiser
Cell proliferation-associated expression of a recently evolved isozyme of triosephosphate isomerase.
Biochemical genetics 1985;23(3-4):267-80.
1985: K H Wurzinger; J E Novotny; Harvey W Mohrenweiser
Studies of the purine analog associated modulation of human erythrocyte acid phosphatase activity.
Molecular and cellular biochemistry 1985;66(2):127-36.
1985: J M Naidu; Harvey W Mohrenweiser
Erythrocyte acid phosphatase: species specificity in activity modulation by purine analogs.
Comparative biochemistry and physiology. B, Comparative biochemistry 1985;81(3):615-9.
1985: J M Naidu; Harvey W Mohrenweiser; J V Nee
A sero-biochemical genetic study of Jalari and Brahmin caste populations of Andhra Pradesh, India.
Human heredity 1985;35(3):148-56.
1984: J V Neel; Harvey W Mohrenweiser
Failure to demonstrate mutations affecting protein structure or function in children with congenital defects or born prematurely.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(17):5499-503.
1984: Francisco M Salzano; Harvey W Mohrenweiser; H Gershowitz; James V Neel; M A Mestriner; A L Simões; J Constans; M J De Melo e Freitas
New studies on the Macushi Indians of northern Brazil.
Annals of human biology 1984;11(4):337-50.
1984: Harvey W Mohrenweiser; J V Neel
A "disproportion" between the frequency of rare electropmorphs and enzyme deficiency variants in Amerindians.
American journal of human genetics 1984;36(3):655-62.
1984: Trudy Turner; P T Wade; Harvey W Mohrenweiser
Variation in erythrocyte enzyme activity among primate species.
Comparative biochemistry and physiology. B, Comparative biochemistry 1984;77(3):541-5.
1984: J M Naidu; Trudy Turner; Harvey W Mohrenweiser
Thermostability characteristics of glucosephosphate and triosephosphate isomerase in erythrocytes from several species.
Comparative biochemistry and physiology. B, Comparative biochemistry 1984;79(2):211-7.
1983: Harvey W Mohrenweiser
Enzyme-deficiency variants: frequency and potential significance in human populations.
Isozymes 1983;10():51-68.
1982: Harvey W Mohrenweiser; S Fielek
Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants.
Pediatric research 1982;16(11):960-3.
1982: K H Wurzinger; Harvey W Mohrenweiser
Studies on the genetic and non-genetic (physiological) variation of human erythrocyte glutamic oxaloacetic transaminase.
Annals of human genetics 1982;46(Pt 3):191-201.
1982: R Barrantes; P E Smouse; James V Neel; Harvey W Mohrenweiser; H Gershowitz
Migration and genetic infrastructure of the Central American Guaymi and their affinities with other tribal groups.
American journal of physical anthropology 1982;58(2):201-14.
1982: Harvey W Mohrenweiser; J E Novotny
ACP1GUA-1--a low-activity variant of human erythrocyte acid phosphatase: association with increased glutathione reductase activity.
American journal of human genetics 1982;34(3):425-33.
1982: Harvey W Mohrenweiser; J E Novotny
An enzymatically inactive variant of human lactate dehydrogenase-LDHBGUA-1. Study of subunit interaction.
Biochimica et biophysica acta 1982;702(1):90-8.
1982: J Asakawa; Harvey W Mohrenweiser
Characterization of two new electrophoretic variants of human triosephosphate isomerase: stability, kinetic, and immunological properties.
Biochemical genetics 1982;20(1-2):59-76.
1982: Harvey W Mohrenweiser; R S Decker
Identification of several electrophoretic variants of human ceruloplasmin including CpMichigan, a new polymorphism.
Human heredity 1982;32(6):369-73.
1981: Harvey W Mohrenweiser; S Fielek; K H Wurzinger
Characteristics of enzymes of erythrocytes from newborn infants and adults: activity, thermostability, and electrophoretic profile as a function of cell age.
American journal of hematology 1981;11(2):125-36.
1981: R S Decker; Harvey W Mohrenweiser
Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus.
American journal of human genetics 1981;33(5):683-91.
1981: Harvey W Mohrenweiser; J V Neel
Frequency of thermostability variants: estimation of total "rare" variant frequency in human populations.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(9):5729-33.
1981: Harvey W Mohrenweiser
Frequency of enzyme deficiency variants in erythrocytes of newborn infants.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(8):5046-50.
1980: C M Yoshihara; Harvey W Mohrenweiser
Characterization of ACP1TIC-1, an electrophoretic variant of erythrocyte acid phosphatase restricted to the Ticuna Indians of central Amazonas.
American journal of human genetics 1980;32(6):898-907.
1980: J V Neel; Harvey W Mohrenweiser; Miriam H Meisler
Rate of spontaneous mutation at human loci encoding protein structure.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(10):6037-41.
1980: James V Neel; H Gershowitz; Harvey W Mohrenweiser; B Amos; D D Kostyu; Francisco M Salzano; M A Mestriner; D Lawrence; A L Simões; P E Smouse; W J Oliver; Richard S Spielman; J V Neel
Genetic studies on the Ticuna, an enigmatic tribe of Central Amazonas.
Annals of human genetics 1980;44(Pt 1):37-54.
1980: H M Moreno Fuenmayor; K L Meilinger; D L Rucknagel; Harvey W Mohrenweiser; E H Chu
Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12.
American journal of medical genetics 1980;7(3):361-8.
1980: R J Feuers; R R Delongchamp; D A Casciano; J G Burkhart; Harvey W Mohrenweiser
Assay for mouse tissue enzymes: levels of activity and statistical variation for 29 enzymes of liver or brain.
Analytical biochemistry 1980;101(1):123-30.
1979: Harvey W Mohrenweiser; R P Erickson
Enzyme changes associated with mitoichondrial malic enzyme deficiency in mice.
Biochimica et biophysica acta 1979;587(3):313-23.
1979: S Fielek; Harvey W Mohrenweiser
Erythrocyte enzyme deficiencies assessed with a miniature centrifugal analyzer.
Clinical chemistry 1979;25(3):384-8.
1979: Harvey W Mohrenweiser; J V Neel; M A Mestriner; F M Salzano; E Migliazza; A L Simões; C M Yoshihara
Electrophoretic variants in three Amerindian tribes: the Baniwa, Kanamari, and Central Pano of western Brazil.
American journal of physical anthropology 1979;50(2):237-46.
1979: C Satoh; Harvey W Mohrenweiser
Genetic heterogeneity within an electrophoretic phenotype of phosphoglucose isomerase in a Japanese population.
Annals of human genetics 1979;42(3):283-92.
1978: J G Burkhart; Harvey W Mohrenweiser
Developmental profile of enzyme activity in several tissues of the C57BL/6 mouse between birth and 35 days of age.
Enzyme 1978;23(4):246-56.
1974: Harvey W Mohrenweiser; H C Pitot
Studies on the mechanism of 5-fluoroorotic acid inhibition of serine dehydratase induction.
Archives of biochemistry and biophysics 1974;164(2):663-8.
1973: Harvey W Mohrenweiser; M B Yatvin; H C Pitot
Interaction of glucagon and catecholamines in the regulation of serine dehydratase.
Endocrinology 1973;93(2):469-77.
1973: Harvey W Mohrenweiser; R S Emery
Hormonal control of precursor pools, ribonucleic acid synthesis, and cellular morphology in mammary tissue pieces during lactogenesis.
Journal of dairy science 1973;56(4):436-45.
1972: Harvey W Mohrenweiser; M B Yatvin
Regulation of serine dehydratase induction in rat liver.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) 1972;141(3):1084-8.
1969: D C Beitz; Harvey W Mohrenweiser; J W Thomas; W A Wod
Synthesis of milk proteins in a cell-free system isolated from lactating bovine mammary tissue.
Archives of biochemistry and biophysics 1969;132(1):210-22.
1968: Harvey W Mohrenweiser; J D Donker
Forage evaluation. 3. Comparison of severalmethds of evaluating two alfalfa hays fed to lactating cows.
Journal of dairy science 1968;51(3):373-7.
1968: J D Donker; H Singh; Harvey W Mohrenweiser
Forage evaluation. I. Performanc of holstein heifers fed only early-cut or late-cut alfalfa hay on a free-choice basis.
Journal of dairy science 1968;51(3):362-6.
1966: M L Fahning; R H Schultz; E F Graham; J D Donker; Harvey W Mohrenweiser
Synchronization of oestrus in dairy heifers with 6-alpha-methyl-17-alpha-acetoxy-progesterone and its effect on conception rate.
Journal of reproduction and fertility 1966;12(3):569-71.