FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Cathy Tuck-Muller

Research Profile

Procedures

Disorders

Anatomy

Living Beings

Infants

Physiology

Pregnancy

Co-author Network

Publications

TOP 3
Tian-Jian Chen; Yueying Wang; Jose E Martinez; Glenn L Wilson; Xi-Yu He; Cathy M Tuck-Muller; Paul Maertens; Wladimir Wertelecki; Tian-Jian Chen
Gene symbol: RPS6KA3.
Yueying Wang; Jose E Martinez; Glenn L Wilson; Xi-Yu He; Cathy M Tuck-Muller; Paul Maertens; Wladimir Wertelecki; Tian-Jian Chen
A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome.
David Gisselsson; Chunbo Shao; Cathy M Tuck-Muller; Suzana Sogorovic; Eva Pålsson; Dominique Smeets; Melanie Ehrlich
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Cathy Tuck-Muller (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2007: Tian-Jian Chen; Yueying Wang; Jose E Martinez; Glenn L Wilson; Xi-Yu He; Cathy M Tuck-Muller; Paul Maertens; Wladimir Wertelecki; Tian-Jian Chen
Gene symbol: RPS6KA3.
Human genetics 2007;121(2):288.
2006: Yueying Wang; Jose E Martinez; Glenn L Wilson; Xi-Yu He; Cathy M Tuck-Muller; Paul Maertens; Wladimir Wertelecki; Tian-Jian Chen
A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome.
American journal of medical genetics. Part A 2006;140(12):1274-9.
2005: David Gisselsson; Chunbo Shao; Cathy M Tuck-Muller; Suzana Sogorovic; Eva Pålsson; Dominique Smeets; Melanie Ehrlich
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells.
Chromosoma 2005;114(2):118-26.
2002: Jonathan G Scammell; J Allan Tucker; Judy A King; Charleen M Moore; James L Wright; Cathy M Tuck-Muller
A kidney epithelial cell line from a Bolivian squirrel monkey.
In vitro cellular & developmental biology. Animal 2002;38(5):258-61.
2002: Weigong He; Cathy M Tuck-Muller; José E Martínez; Shibo Li; Ewellonda R Rowley; Wladimir Wertelecki
Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts.
American journal of medical genetics 2002;107(1):12-7.
2001: Melanie Ehrlich; F Tsien; D Herrera; V Blackman; J Roggenbuck; Cathy M Tuck-Muller
High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample.
Journal of medical genetics 2001;38(12):882-4.
2001: Cathy M Tuck-Muller; Barbara K Goodman; Shibo Li; Jose E Martinez; Xiao-Ning Chen; Wladimir Wertelecki; Julie R Korenberg; Gail Stetten
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(2):126-31.
2001: Jonathan G Scammell; J L Wright; Cathy M Tuck-Muller
The origin of four squirrel monkey cell lines established by karyotype analysis.
Cytogenetics and cell genetics 2001;93(3-4):263-4.
2000: A Narayan; Cathy M Tuck-Muller; K Weissbecker; Dominique Smeets; Melanie Ehrlich
Hypersensitivity to radiation-induced non-apoptotic and apoptotic death in cell lines from patients with the ICF chromosome instability syndrome.
Mutation research 2000;456(1-2):1-15.
2000: H Chen; X Mu; T Sonoda; K C Kim; K Dailey; J Martinez; Cathy M Tuck-Muller; W Wertelecki
FGFR3 gene mutation (Gly380Arg) with achondroplasia and i(21q) Down syndrome: phenotype-genotype correlation.
Southern medical journal 2000;93(6):622-4.
2000: Cathy M Tuck-Muller; A Narayan; F Tsien; Dominique Smeets; J Sawyer; Emerich Fiala; Ock Soon Sohn; Melanie Ehrlich
DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
Cytogenetics and cell genetics 2000;89(1-2):121-8.
1999: Hans Andersson; J Frentz; José E Martínez; Cathy M Tuck-Muller; J Bellizaire
Adrenal insufficiency in Smith-Lemli-Opitz syndrome.
American journal of medical genetics 1999;82(5):382-4.
1999: José E Martínez; Cathy M Tuck-Muller; W Gasparrini; Shibo Li; Wladimir Wertelecki
1p microdeletion in sibs with minimal phenotypic manifestations.
American journal of medical genetics 1999;82(2):107-9.
1998: Shibo Li; Cathy M Tuck-Muller; José E Martínez; E R Rowley; H Chen; Wladimir Wertelecki
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH).
American journal of medical genetics 1998;80(5):487-90.
1996: Cathy M Tuck-Muller; M Varela; Shibo Li; G Pridjian; H Chen; Wladimir Wertelecki
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring.
American journal of medical genetics 1996;63(2):392-5.
1995: Cathy M Tuck-Muller; H Chen; José E Martínez; C C Shen; Shibo Li; C Kusyk; Denise A S Batista; Yogendra Bhatnagar; E Dowling; Wladimir Wertelecki
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature.
Human genetics 1995;96(1):119-29.
1995: Cathy M Tuck-Muller; P R Dyken; Shibo Li; H Chen; Elise Labbé; Wladimir Wertelecki
Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease).
American journal of medical genetics 1995;57(2):168-71.
1995: H Chen; Cathy M Tuck-Muller; Denise A S Batista; Wladimir Wertelecki
Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
American journal of medical genetics 1995;56(2):219-33.
1995: Barbara R Migeon; Gail Stetten; Cathy M Tuck-Muller; Joyce Axelman; M Jani; D Dungy
Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation.
Somatic cell and molecular genetics 1995;21(2):113-20.
1995: H Chen; William H Hoffman; C J Kusyk; Cathy M Tuck-Muller; M G Hoffman; L S Davis
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal gland.
American journal of medical genetics 1995;55(4):489-93.
1995: Shibo Li; Cathy M Tuck-Muller; Q Yan; Wladimir Wertelecki; H Chen
A rapid method for PCR amplification of DNA directly from cells fixed in Carnoy's fixative.
American journal of medical genetics 1995;55(1):116-9.
1995: W Ahmad; S Li; H Chen; Cathy M Tuck-Muller; Steven J Pittler; N N Aronson
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22.
Cytogenetics and cell genetics 1995;71(1):44-6.
1994: R D Peterson; Cathy M Tuck-Muller; Joseph A Spinnato; K Peevy; K Giattina; C Hoff
An HLA-haplotype associated with preeclampsia and intrauterine growth retardation.
American journal of reproductive immunology (New York, N.Y. : 1989) 1994;31(4):177-9.
1994: P Arn; H Chen; Cathy M Tuck-Muller; C Mankinen; G Wachtel; Shibo Li; C C Shen; Stephen S Wachtel
SRVX, a sex reversing locus in Xp21.2-->p22.11.
Human genetics 1994;93(4):389-93.
1994: H Chen; C J Kusyk; Cathy M Tuck-Muller; J E Martinez; R D Dorand; Wladimir Wertelecki
Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
American journal of medical genetics 1994;50(1):28-31.
1993: Denise A S Batista; Cathy M Tuck-Muller; J E Martinez; William G Kearns; P L Pearson; Gail Stetten
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization.
Human genetics 1993;92(2):117-21.
1993: Cathy M Tuck-Muller; J E Martinez; Denise A S Batista; William G Kearns; Wladimir Wertelecki
Duplication of the short arm of the X chromosome in mother and daughter.
Human genetics 1993;91(4):395-400.
1993: José E Martínez; Cathy M Tuck-Muller; D Superneau; Wladimir Wertelecki
Fertility and the cri du chat syndrome.
Clinical genetics 1993;43(4):212-4.
1993: Ethylin Jabs; Cathy M Tuck-Muller; Grant J Anhalt; William C Earnshaw; Robert Wise; Fredrick M Wigley
Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodies.
Cytogenetics and cell genetics 1993;63(3):169-75.
1992: R D Peterson; Jane D Funkhouser; Cathy M Tuck-Muller; R A Gatti
Cancer susceptibility in ataxia-telangiectasia.
Leukemia 1992;6 Suppl 1():8-13.
1991: Ethylin Jabs; Cathy M Tuck-Muller; R Cusano; Jerome B Rattner
Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism.
Chromosoma 1991;100(4):251-61.
1990: Gail Stetten; Cathy M Tuck-Muller; Karin J Blakemore; C Wong; Haig Kazazian ; S E Antonarakis
Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
Molecular biology & medicine 1990;7(6):479-84.
1989: Ethylin Jabs; Cathy M Tuck-Muller; R Cusano; Jerome B Rattner
Centromere separation and aneuploidy in human mitotic mutants: Roberts syndrome.
Progress in clinical and biological research 1989;318():111-8.
1988: A D Ackerman; James C Fackler; Cathy M Tuck-Muller; M M Tarpey; Bruce Freeman; Mark Charles Rogers
Partial monosomy 21, diminished activity of superoxide dismutase, and pulmonary oxygen toxicity.
The New England journal of medicine 1988;318(25):1666-9.
1988: H Youssoufian; Phillip F Chance; Cathy M Tuck-Muller; Ethylin Jabs
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene.
Human genetics 1988;78(3):267-70.
1984: Cathy M Tuck-Muller; B L Bordson; M M Kane; A E Hamilton
A method for combined C-banding and silver staining.
Stain technology 1984;59(5):265-8.
1984: Cathy M Tuck-Muller; B L Bordson; M Varela; J W Bennett
NOR associations with heterochromatin.
Cytogenetics and cell genetics 1984;38(3):165-70.