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Antonio Baldini

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Chunhong Liu; Sei-Ichi Matsui; Masae Morishima; Norma J Nowak; Annie Pao; Michael S Parmacek; Tao Yu; Antonio Baldini; Alberto Costa; John Kenneth Cowell; Dawei Fu; Katheleen J Gardiner; Ping Liang; Li Zhang; Normal J Nowak; Y Eugene Yu
Genetic analysis of Down syndrome-associated heart defects in mice.
Tao Yu; Chunhong Liu; Pavel Belichenko; Steven J Clapcote; Shaomin Li; Annie Pao; Alexander Kleschevnikov; Allison R Bechard; Suhail Asrar; Rongqing Chen; Ni Fan; Zhenyu Zhou; Zhengping Jia; Chu Chen; John C Roder; Bin Liu; Antonio Baldini; William C Mobley; Y Eugene Yu
Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice.
Zhen Zhang; Antonio Baldini
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene.

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All Publications

2011: Chunhong Liu; Sei-Ichi Matsui; Masae Morishima; Norma J Nowak; Annie Pao; Michael S Parmacek; Tao Yu; Antonio Baldini; Alberto Costa; John Kenneth Cowell; Dawei Fu; Katheleen J Gardiner; Ping Liang; Li Zhang; Normal J Nowak; Y Eugene Yu
Genetic analysis of Down syndrome-associated heart defects in mice.
Human genetics 2011;130(5):623-32.
2010: Tao Yu; Chunhong Liu; Pavel Belichenko; Steven J Clapcote; Shaomin Li; Annie Pao; Alexander Kleschevnikov; Allison R Bechard; Suhail Asrar; Rongqing Chen; Ni Fan; Zhenyu Zhou; Zhengping Jia; Chu Chen; John C Roder; Bin Liu; Antonio Baldini; William C Mobley; Y Eugene Yu
Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice.
Brain research 2010;1366():162-71.
2010: Zhen Zhang; Antonio Baldini
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2010;21(11-12):556-64.
2010: Huojun Cao; Sergio Florez; Melanie Amen; Tuong Huynh; Ziedonis Skobe; Antonio Baldini; Brad A Amendt
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21.
Developmental biology 2010;347(2):289-300.
2010: Francesca Vitelli; Gabriella Lania; Tuong Huynh; Antonio Baldini
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8.
Journal of molecular and cellular cardiology 2010;49(5):836-40.
2010: Tao Yu; Steven J Clapcote; Zhongyou Li; Chunhong Liu; Annie Pao; Allison R Bechard; Sandra Carattini-Rivera; Sei-Ichi Matsui; John C Roder; Antonio Baldini; William C Mobley; Allan Bradley; Y Eugene Yu
Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2010;21(5-6):258-67.
2010: Li Chen; Annalisa Mupo; Tuong Huynh; Sara Cioffi; Matthew Woods; Chengliu Jin; Wallace McKeehan; LuAnn Thompson-Snipes; Antonio Baldini; Elizabeth Illingworth
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development.
The Journal of cell biology 2010;189(3):417-24.
2007: huansheng xu; Li Chen; Antonio Baldini
In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea.
Developmental biology 2007;310(2):329-40.
2007: Tuong Huynh; Li Chen; Phillip Terrell; Antonio Baldini
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field.
Genesis (New York, N.Y. : 2000) 2007;45(7):470-5.
2007: Di Ai; Xueyao Fu; Jun Wang; Mei-Fang Lu; Li Chen; Antonio Baldini; William H Klein; James F Martin
Canonical Wnt signaling functions in second heart field to promote right ventricular growth.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(22):9319-24.
2007: huansheng xu; Antonio Baldini
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.
Seminars in cell & developmental biology 2007;18(1):77-83.
2007: Akbar Dastjerdi; Lesley Robson; Rebecca Walker; Julia Hadley; Zhen Zhang; Marc Rodriguez-Niedenführ; Paris Ataliotis; Antonio Baldini; Peter J Scambler; Philippa Francis-West
Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm.
Developmental dynamics : an official publication of the American Association of Anatomists 2007;236(2):353-63.
2006: Feiyan Dong; Xiaoxia Sun; Wei Liu; Di Ai; Elizabetha Klysik; Mei-Fang Lu; Julia Hadley; Laurent Antoni; Li Chen; Antonio Baldini; Philippa Francis-West; James F Martin
Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle.
Development (Cambridge, England) 2006;133(24):4891-9.
2006: Catherine Roberts; Sarah Ivins; Andrew Cook; Antonio Baldini; Peter J Scambler
Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
Human molecular genetics 2006;15(23):3394-410.
2006: Min Xie; Dou Zhang; Jason R B Dyck; Yi Li; Hui Zhang; Masae Morishima; Douglas L Mann; George E Taffet; Antonio Baldini; Dirar S Khoury; Michael D Schneider
A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(46):17378-83.
2006: Zhen Zhang; Tuong Huynh; Antonio Baldini
Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development.
Development (Cambridge, England) 2006;133(18):3587-95.
2006: Francesca Vitelli; Zhen Zhang; Tuong Huynh; Angela Sobotka; Annalisa Mupo; Antonio Baldini
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.
Developmental biology 2006;295(2):559-70.
2006: Y Eugene Yu; Masae Morishima; Annie Pao; Ding-Yan Wang; Xiao-Yan Wen; Antonio Baldini; Allan Bradley
A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.
Genetics 2006;173(1):297-307.
2006: Antonio Baldini
The 22q11.2 deletion syndrome: a gene dosage perspective.
TheScientificWorldJournal 2006;6():1881-7.
2005: Zhen Zhang; Fabiana Cerrato; huansheng xu; Francesca Vitelli; Masae Morishima; Joshua Vincentz; Yasuhide Furuta; Lijiang Ma; James F Martin; Antonio Baldini; Elizabeth Lindsay
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Development (Cambridge, England) 2005;132(23):5307-15.
2005: huansheng xu; Fabiana Cerrato; Antonio Baldini
Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion.
Development (Cambridge, England) 2005;132(19):4387-95.
2005: Sarah Ivins; Kelly Lammerts van Beuren; Catherine Roberts; Chela T James; Elizabeth Lindsay; Antonio Baldini; Paris Ataliotis; Peter J Scambler
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
Developmental biology 2005;285(2):554-69.
2005: Antonio Baldini
Dissecting contiguous gene defects: TBX1.
Current opinion in genetics & development 2005;15(3):279-84.
2005: Katrina Prescott; Sarah Ivins; Mike Hubank; Elizabeth Lindsay; Antonio Baldini; Peter J Scambler
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.
Human genetics 2005;116(6):486-96.
2004: huansheng xu; Masae Morishima; John N Wylie; Robert J Schwartz; Benoit G Bruneau; Elizabeth Lindsay; Antonio Baldini
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
Development (Cambridge, England) 2004;131(13):3217-27.
2004: Antonio Baldini
DiGeorge syndrome: an update.
Current opinion in cardiology 2004;19(3):201-4.
2003: Francesca Vitelli; Antonio Baldini
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
Trends in genetics : TIG 2003;19(11):588-93.
2003: Antonio Baldini
DiGeorge's syndrome: a gene at last.
Lancet 2003;362(9393):1342-3.
2003: Masae Morishima; Hiromi Yanagisawa; Masashi Yanagisawa; Antonio Baldini
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
Developmental dynamics : an official publication of the American Association of Anatomists 2003;228(1):95-104.
2003: Francesca Vitelli; Antonella Viola; Masae Morishima; Tiziano Pramparo; Antonio Baldini; Elizabeth Lindsay
TBX1 is required for inner ear morphogenesis.
Human molecular genetics 2003;12(16):2041-8.
2002: Antonio Baldini
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
Human molecular genetics 2002;11(20):2363-9.
2002: Francesca Vitelli; Ilaria Taddei; Masae Morishima; Erik N Meyers; Elizabeth Lindsay; Antonio Baldini
A genetic link between Tbx1 and fibroblast growth factor signaling.
Development (Cambridge, England) 2002;129(19):4605-11.
2002: Francesca Vitelli; Masae Morishima; Ilaria Taddei; Elizabeth Lindsay; Antonio Baldini
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
Human molecular genetics 2002;11(8):915-22.
2002: Francesca Vitelli; Elizabeth Lindsay; Antonio Baldini
Genetic dissection of the DiGeorge syndrome phenotype.
Cold Spring Harbor symposia on quantitative biology 2002;67():327-32.
2001: Richard Paylor; Kellie L McIlwain; R McAninch; A Nellis; Lisa A Yuva-Paylor; Antonio Baldini; Elizabeth Lindsay
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
Human molecular genetics 2001;10(23):2645-50.
2001: Elizabeth Lindsay; Antonio Baldini
Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region.
Human molecular genetics 2001;10(9):997-1002.
2001: Elizabeth Lindsay; Francesca Vitelli; H Su; Masae Morishima; Tuong Huynh; Tiziano Pramparo; V Jurecic; G Ogunrinu; H F Sutherland; Peter J Scambler; Allan Bradley; Antonio Baldini
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
Nature 2001;410(6824):97-101.
2001: Qing Wang; Ayse Anil Timur; Przemyslaw Szafranski; A Sadgephour; V Jurecic; John Kenneth Cowell; Antonio Baldini; David J Driscoll
Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome.
Cytogenetics and cell genetics 2001;95(3-4):183-8.
2001: K Ogura; K Matsumoto; A Kuroiwa; T Isobe; T Otoguro; V Jurecic; Antonio Baldini; Y Matsuda; T Ogura
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes.
Cytogenetics and cell genetics 2001;92(3-4):320-5.
1999: Elizabeth Lindsay; A Botta; V Jurecic; S Carattini-Rivera; Y C Cheah; Howard M Rosenblatt; Allan Bradley; Antonio Baldini
Congenital heart disease in mice deficient for the DiGeorge syndrome region.
Nature 1999;401(6751):379-83.
1999: G Ning; V Jurecic; Antonio Baldini; Jianming Xu
Structure and chromosomal locations of mouse steroid receptor coactivator gene family.
In vitro cellular & developmental biology. Animal 1999;35(8):481-6.
1999: Y Cao; HL Kang; X Xu; M Wang; S H Dho; Jun R Huh; B J Lee; Francis Kalush; D Bocskai; Y Ding; JG Tesmer; J Lee; E Moon; V Jurecic; Antonio Baldini; Heinz-Ulrich G Weier; Norman A Doggett; MI Simon; Mark D Adams; UJ Kim
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2.
Genome research 1999;9(8):763-74.
1998: Elizabeth Lindsay; Antonio Baldini
Congenital heart defects and 22q11 deletions: which genes count?
Molecular medicine today 1998;4(8):350-7.
1998: Ignatia B Van den Veyver; Trena A Cormier; V Jurecic; Antonio Baldini; Huda Y Zoghbi
Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22.
Genomics 1998;51(2):251-61.
1998: Elizabeth Lindsay; E L Harvey; Peter J Scambler; Antonio Baldini
ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene.
Human molecular genetics 1998;7(4):629-35.
1997: OA Cabello; Antonio Baldini; Manzoor Bhat; H Bellen; John W Belmont
Localization of BRRN1, the human homologue of Drosophila barr, to 2q11.2.
Genomics 1997;46(2):311-3.
1997: A Pragliola; V Jurecic; C K Chau; N Philip; Antonio Baldini
Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.
American journal of human genetics 1997;61(6):1456-9.
1997: A Botta; Elizabeth Lindsay; V Jurecic; Antonio Baldini
Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(12):890-5.
1997: M Dasouki; V Jurecic; John A Phillips; J A Whitlock; Antonio Baldini
DiGeorge anomaly and chromosome 10p deletions: one or two loci?
American journal of medical genetics 1997;73(1):72-5.
1997: William J Craigen; Elizabeth Lindsay; J T Bricker; Edith P Hawkins; Antonio Baldini
Deletion of chromosome 22q11 and pseudohypoparathyroidism.
American journal of medical genetics 1997;72(1):63-5.
1997: Katalin Banki; RL Eddy; TB Shows; D L Halladay; F Bullrich; C M Croce; V Jurecic; Antonio Baldini; Andras Perl
The human transaldolase gene (TALDO1) is located on chromosome 11 at p15.4-p15.5.
Genomics 1997;45(1):233-8.
1997: Mark B Lewin; Elizabeth Lindsay; V Jurecic; Veronica K Goytia; Jeffrey A Towbin; Antonio Baldini
A genetic etiology for interruption of the aortic arch type B.
The American journal of cardiology 1997;80(4):493-7.
1997: P Rizzu; Bassem R Haddad; isabel vallcorba; A Alonso; M Teresa Ferro; Jose M Garcia-Sagredo; Antonio Baldini
Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
American journal of medical genetics 1997;68(4):428-32.
1997: Elizabeth Lindsay; Antonio Baldini
A mouse gene (Dgcr6) related to the Drosophila gonadal gene is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome.
Cytogenetics and cell genetics 1997;79(3-4):243-7.
1997: A Botta; V Jurecic; A Pizzuti; G Novelli; B Dallapiccola; Antonio Baldini
Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene.
Cytogenetics and cell genetics 1997;77(3-4):264-5.
1996: R C Juyal; A Kuwano; I Kondo; F Zara; Antonio Baldini; Pragna I Patel
Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
American journal of medical genetics 1996;66(2):193-6.
1996: Barbara J Trask; Heather C Mefford; Ger van den Engh; Hillary F Massa; R C Juyal; Lorraine Potocki; B Finucane; D N Abuelo; D R Witt; E Magenis; Antonio Baldini; F Greenberg; James R Lupski; Pragna I Patel
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients.
Human genetics 1996;98(6):710-8.
1996: P Rizzu; Elizabeth Lindsay; C Taylor; H O'Donnell; A Levy; Peter J Scambler; Antonio Baldini
Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(9):639-43.
1996: Evan E Eichler; F Lu; Y Shen; Rachele Antonacci; V Jurecic; Norman A Doggett; R K Moyzis; Antonio Baldini; Richard A Gibbs; David L Nelson
Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
Human molecular genetics 1996;5(7):899-912.
1996: H F Sutherland; R Wadey; J M McKie; C Taylor; U Atif; K A Johnstone; Stephanie Halford; UJ Kim; Judith A Goodship; Antonio Baldini; Peter J Scambler
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.
American journal of human genetics 1996;59(1):23-31.
1996: R C Juyal; Luis Figuera; X Hauge; Sarah H Elsea; James R Lupski; F Greenberg; Antonio Baldini; Pragna I Patel
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.
American journal of human genetics 1996;58(5):998-1007.
1996: Elizabeth Lindsay; P Rizzu; Rachele Antonacci; V Jurecic; J Delmas-Mata; Cheng Chi Lee; UJ Kim; Peter J Scambler; Antonio Baldini
A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.
Genomics 1996;32(1):104-12.
1995: Sarah H Elsea; R C Juyal; S Jiralerspong; B M Finucane; Massimo Pandolfo; F Greenberg; Antonio Baldini; P Stover; Pragna I Patel
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.
American journal of human genetics 1995;57(6):1342-50.
1995: R C Juyal; B Finucane; L G Shaffer; James R Lupski; F Greenberg; C I Scott; Antonio Baldini; Pragna I Patel
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient.
American journal of medical genetics 1995;59(3):406-7.
1995: R C Juyal; F Greenberg; G A Mengden; James R Lupski; Barbara J Trask; Ger van den Engh; Elizabeth Lindsay; H Christy; Ken-Shiung Chen; Antonio Baldini
Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization.
American journal of medical genetics 1995;58(3):286-91.
1995: K C Worley; Elizabeth Lindsay; W Bailey; J Wise; Edward RB McCabe; Antonio Baldini
Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiency.
American journal of medical genetics 1995;57(4):615-9.
1995: Elizabeth Lindsay; R Goldberg; V Jurecic; Bernice E Morrow; C Carlson; Raju Kucherlapati; Robert J Shprintzen; Antonio Baldini
Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
American journal of medical genetics 1995;57(3):514-22.
1995: Z Zhao; Cheng Chi Lee; Antonio Baldini; CT Caskey
A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1.
Genomics 1995;27(2):370-3.
1995: L Abu-Elheiga; A Jayakumar; Antonio Baldini; Subrahmanyam S Chirala; Salih J Wakil
Human acetyl-CoA carboxylase: characterization, molecular cloning, and evidence for two isoforms.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(9):4011-5.
1995: Elizabeth Lindsay; Lisa Shaffer; R Carrozzo; F Greenberg; Antonio Baldini
De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.
American journal of medical genetics 1995;56(3):296-9.
1995: Z Zhao; Cheng Chi Lee; S Jiralerspong; R C Juyal; F Lu; Antonio Baldini; F Greenberg; CT Caskey; Pragna I Patel
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.
Human molecular genetics 1995;4(4):589-97.
1995: Elizabeth Lindsay; F Greenberg; Lisa Shaffer; Stuart K Shapira; Peter J Scambler; Antonio Baldini
Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
American journal of medical genetics 1995;56(2):191-7.
1995: Avi Orr-Urtreger; Michael F Seldin; Antonio Baldini; Arthur L Beaudet
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor.
Genomics 1995;26(2):399-402.
1995: Rachele Antonacci; Mariano Rocchi; Nicoletta Archidiacono; Antonio Baldini
Ordered mapping of three alpha satellite DNA subsets on human chromosome 22.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1995;3(2):124-7.
1995: M S Aqua; P Rizzu; Elizabeth Lindsay; Lisa Shaffer; E H Zackai; J Overhauser; Antonio Baldini
Duplication 3q syndrome: molecular delineation of the critical region.
American journal of medical genetics 1995;55(1):33-7.
1995: R D Knapp; Louis C Smith; Antonio Baldini
Eigenanalysis of DAPI-stained chromosomes: tools and strategies toward computer-assisted analysis of FISH experiments.
Cytogenetics and cell genetics 1995;69(1-2):81-6.
1995: P Rizzu; Antonio Baldini
Three members of the human cystatin gene superfamily, AHSG, HRG, and KNG, map within one megabase of genomic DNA at 3q27.
Cytogenetics and cell genetics 1995;70(1-2):26-8.
1995: B Haddad; Rachele Antonacci; P Rizzu; Elizabeth Lindsay; M R Hughes; Louis C Smith; R D Knapp; Antonio Baldini
Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis.
Cytogenetics and cell genetics 1995;71(3):276-9.
1994: P Rizzu; Antonio Baldini
Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome.
Genomics 1994;24(3):580-2.
1994: A Jayakumar; Subrahmanyam S Chirala; A Craig Chinault; Antonio Baldini; L Abu-Elheiga; Salih J Wakil
Isolation and chromosomal mapping of genomic clones encoding the human fatty acid synthase gene.
Genomics 1994;23(2):420-4.
1994: Mariano Rocchi; Nicoletta Archidiacono; Rachele Antonacci; P Finelli; L D'Aiuto; Rocco Carbone; Elizabeth Lindsay; Antonio Baldini
Cloning and comparative mapping of recently evolved human chromosome 22-specific alpha satellite DNA.
Somatic cell and molecular genetics 1994;20(5):443-8.
1994: Paul Lau; H J Zhu; Antonio Baldini; C Charnsangavej; Lawrence Chan
Dimeric structure of a human apolipoprotein B mRNA editing protein and cloning and chromosomal localization of its gene.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(18):8522-6.
1994: Kazuhiro Oka; K W Tzung; M Sullivan; Elizabeth Lindsay; Antonio Baldini; Lawrence Chan
Human very-low-density lipoprotein receptor complementary DNA and deduced amino acid sequence and localization of its gene (VLDLR) to chromosome band 9p24 by fluorescence in situ hybridization.
Genomics 1994;20(2):298-300.
1994: Elizabeth Lindsay; A Grillo; GB Ferrero; E J Roth; E Magenis; Markus Grompe; M Hultén; C Gould; Antonio Baldini; Huda Y Zoghbi
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.
American journal of medical genetics 1994;49(2):229-34.
1994: Antonio Baldini; Elizabeth Lindsay
Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies.
Methods in molecular biology (Clifton, N.J.) 1994;33():75-84.
1993: A Gregory Matera; Antonio Baldini; David C Ward
An oligonucleotide probe specific to the centromeric region of human chromosome 5.
Genomics 1993;18(3):729-31.
1993: Stephanie Halford; R Wadey; Catherine Roberts; S C Daw; J A Whiting; H O'Donnell; I Dunham; D Bentley; Elizabeth Lindsay; Antonio Baldini
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
Human molecular genetics 1993;2(12):2099-107.
1993: Elizabeth Lindsay; Stephanie Halford; R Wadey; Peter J Scambler; Antonio Baldini
Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
Genomics 1993;17(2):403-7.
1993: Stephanie Halford; Elizabeth Lindsay; M Nayudu; A H Carey; Antonio Baldini; Peter J Scambler
Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.
Human molecular genetics 1993;2(2):191-6.
1993: Antonio Baldini; T Ried; V Shridhar; K Ogura; L D'Aiuto; Mariano Rocchi; David C Ward
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13.
Human genetics 1993;90(6):577-83.
1992: Jacob W Ijdo; E A Lindsay; R A Wells; Antonio Baldini
Multiple variants in subtelomeric regions of normal karyotypes.
Genomics 1992;14(4):1019-25.
1992: R Dante; Maire E Percy; Antonio Baldini; V D Markovic; D A Miller; M Rocchi; Alain Niveleau; O J Miller
Methylation of the 5' flanking sequences of the ribosomal DNA in human cell lines and in a human-hamster hybrid cell line.
Journal of cellular biochemistry 1992;50(4):357-62.
1992: Jacob W Ijdo; Antonio Baldini; R A Wells; David C Ward; S T Reeders
FRA2B is distinct from inverted telomere repeat arrays at 2q13.
Genomics 1992;12(4):833-5.
1992: D G Ginzinger; V Shridhar; Antonio Baldini; R T Taggart; O J Miller; David I Smith
The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3.
American journal of human genetics 1992;50(4):826-33.
1992: T Ried; Antonio Baldini; T C Rand; David C Ward
Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(4):1388-92.
1992: Antonio Baldini; Nicoletta Archidiacono; Rocco Carbone; A Bolino; V Shridhar; O J Miller; D A Miller; David C Ward; Mariano Rocchi
Isolation and comparative mapping of a human chromosome 20-specific alpha-satellite DNA clone.
Cytogenetics and cell genetics 1992;59(1):12-6.
1991: Antonio Baldini; D A Miller; V Shridhar; Mariano Rocchi; O J Miller; David C Ward
Comparative mapping of a gorilla-derived alpha satellite DNA clone on great ape and human chromosomes.
Chromosoma 1991;101(2):109-14.
1991: Jacob W Ijdo; Antonio Baldini; David C Ward; S T Reeders; R A Wells
Origin of human chromosome 2: an ancestral telomere-telomere fusion.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(20):9051-5.
1991: Jacob W Ijdo; R A Wells; Antonio Baldini; S T Reeders
Improved telomere detection using a telomere repeat probe (TTAGGG)n generated by PCR.
Nucleic acids research 1991;19(17):4780.
1991: Antonio Baldini; David C Ward
In situ hybridization banding of human chromosomes with Alu-PCR products: a simultaneous karyotype for gene mapping studies.
Genomics 1991;9(4):770-4.
1991: Antonio Baldini; D A Miller; O J Miller; O A Ryder; A R Mitchell
A chimpanzee-derived chromosome-specific alpha satellite DNA sequence conserved between chimpanzee and human.
Chromosoma 1991;100(3):156-61.
1990: M Rocchi; Antonio Baldini; N Archidiacono; S Lainwala; O J Miller; D A Miller
Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone.
Genomics 1990;8(4):705-9.
1990: Antonio Baldini; M Rocchi; N Archidiacono; O J Miller; D A Miller
A human alpha satellite DNA subset specific for chromosome 12.
American journal of human genetics 1990;46(4):784-8.
1989: Antonio Baldini; David I Smith; M Rocchi; O J Miller; D A Miller
A human alphoid DNA clone from the EcoRI dimeric family: genomic and internal organization and chromosomal assignment.
Genomics 1989;5(4):822-8.
1988: Adriana de Capoa; M P Felli; Antonio Baldini; M Rocchi; N Archidiacono; C Aleixandre; O J Miller; D A Miller
Relationship between the number and function of human ribosomal genes.
Human genetics 1988;79(4):301-4.
1988: G L Spadoni; Stefano Cianfarani; Antonio Baldini; Linda Ravenna; M P Felli; A Camaioni; M L Manca Bitti; G Sciré; Brunetto Boscherini; Adriana de Capoa
Laron dwarfism: cellular unresponsiveness to GH demonstrated on cultured lymphocytes by a cytochemical method.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 1988;20(7):450-2.
1988: Antonio Baldini; M P Felli; Linda Ravenna; A Camaioni; Adriana de Capoa; G L Spadoni; Stefano Cianfarani; Brunetto Boscherini
Differential ribosomal gene responsiveness to human growth hormone is visualized by selective silver staining.
Cytogenetics and cell genetics 1988;47(1-2):22-5.
1986: Adriana de Capoa; P Marlekaj; Antonio Baldini; M P Felli; M Rocchi; N Archidiacono; Stefano Cianfarani; G L Spadoni; Brunetto Boscherini
Growth hormone-induced regulation of rRNA gene activity in human cultured cells.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 1986;18(8):574-5.
1985: Adriana de Capoa; Antonio Baldini; P Marlekaj; C Natoli; M Rocchi; N Archidiacono; Stefano Cianfarani; G L Spadoni; Brunetto Boscherini
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs.
Cell biology international reports 1985;9(9):791-6.
1985: Adriana de Capoa; P Marlekaj; Antonio Baldini; N Archidiacono; M Rocchi
The transcriptional activity of individual ribosomal DNA gene clusters is modulated by serum concentration.
Journal of cell science 1985;74():21-35.
1985: Adriana de Capoa; P Marlekaj; Antonio Baldini; M Rocchi; N Archidiacono
Cytologic demonstration of differential activity of rRNA gene clusters in different human tissues.
Human genetics 1985;69(3):212-7.