Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome
Kahlem, Pascal, Sultan, Marc, Herwig, Ralf, Steinfath, Matthias, Balzereit, Daniela, Eppens, Barbara, Saran, Nidhi G, Pletcher, Mathew T, South, Sarah T, Stetten, Gail, Lehrach, Hans, Reeves, Roger H, Yaspo, Marie-Laure
Published in Genome research (01.07.2004)
Published in Genome research (01.07.2004)
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Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres
Warburton, Peter E., Cooke, Carol A., Bourassa, Sylvie, Vafa, Omid, Sullivan, Beth A., Stetten, Gail, Gimelli, Giorgio, Warburton, Dorothy, Tyler-Smith, Chris, Sullivan, Kevin F., Poirier, Guy G., Earnshaw, William C.
Published in Current biology (01.11.1997)
Published in Current biology (01.11.1997)
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X-linked adrenoleukodystrophy : Genes, mutations, and phenotypes
SMITH, K. D, KEMP, S, BRAITERMAN, L. T, LU, J.-F, WEI, H.-M, GERAGHTY, M, STETTEN, G, BERGIN, J. S, PEVSNER, J, WATKINS, P. A
Published in Neurochemical research (1999)
Published in Neurochemical research (1999)
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Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome
Norris, R A, Scott, K K, Moore, C S, Stetten, G, Brown, C R, Jabs, E W, Wulfsberg, E A, Yu, J, Kern, M J
Published in Mammalian genome (01.11.2000)
Published in Mammalian genome (01.11.2000)
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X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism
Wang, Ying, Busin, Rachel, Reeves, Catherine, Bezman, Lena, Raymond, Gerald, Toomer, Cicely J., Watkins, Paul A., Snowden, Ann, Moser, Ann, Naidu, Sakkubai, Bibat, Genila, Hewson, Stacy, Tam, Karen, Clarke, Joe T.R., Charnas, Lawrence, Stetten, Gail, Karczeski, Barbara, Cutting, Garry, Steinberg, Steven
Published in Molecular genetics and metabolism (01.09.2011)
Published in Molecular genetics and metabolism (01.09.2011)
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TRPC1, a Human Homolog of a Drosophila Store-Operated Channel
Wes, Paul D., Chevesich, Jorge, Jeromin, Andreas, Rosenberg, Carla, Stetten, Gail, Montell, Craig
Published in Proceedings of the National Academy of Sciences - PNAS (10.10.1995)
Published in Proceedings of the National Academy of Sciences - PNAS (10.10.1995)
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In utero Hematopoietic Stem Cell Transplantation in Canines: Exploring the Gestational Age Window of Opportunity to Maximize Engraftment
Petersen, Scott M., Gendelman, Mariya, Murphy, Kathleen M., Torbenson, Michael, Jones, Richard J., Stetten, Gail, Bird, Chris, Blakemore, Karin J.
Published in Fetal diagnosis and therapy (01.01.2013)
Published in Fetal diagnosis and therapy (01.01.2013)
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Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization
Cain, Colyn Cargile, Saul, Daniel, Attanasio, Lisa, Oehler, Erin, Hamosh, Ada, Blakemore, Karin, Stetten, Gail
Published in Prenatal diagnosis (01.04.2007)
Published in Prenatal diagnosis (01.04.2007)
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Frequency of chromosomal abnormalities in spontaneous abortions derived from intracytoplasmic sperm injection compared with those from in vitro fertilization
Ma, Sai, Philipp, Tom, Zhao, Yulian, Stetten, Gail, Robinson, Wendy P., Kalousek, Dagmar
Published in Fertility and sterility (2006)
Published in Fertility and sterility (2006)
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In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model
Blakemore, Karin, Hattenburg, Catherine, Stetten, Gail, Berg, Karin, South, Sarah, Murphy, Kathleen, Jones, Richard
Published in American journal of obstetrics and gynecology (01.04.2004)
Published in American journal of obstetrics and gynecology (01.04.2004)
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568: Chromosome microarray analysis for prenatal diagnosis - first steps in integration into current practice
Batista, Denise, Cain, Colyn, Saul, Dan, Dowey, Sarah, Beierl, Katie, Blakemore, Karin, Stetten, Gail
Published in American journal of obstetrics and gynecology (2007)
Published in American journal of obstetrics and gynecology (2007)
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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
Dietz, Harry C, Cutting, Carry R, Pyeritz, Reed E, Maslen, Cheryl L, Sakai, Lynn Y, Corson, Glen M, Puffenberger, Erik G, Hamosh, Ada, Nanthakumar, Elizabeth J, Curristin, Sheila M, Stetten, Gail, Meyers, Deborah A, Francomano, Clair A
Published in Nature (London) (25.07.1991)
Published in Nature (London) (25.07.1991)
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Reevaluating confined placental mosaicism
Stetten, Gail, Escallon, Cathleen S., South, Sarah T., McMichael, Joseph L., Saul, Daniel O., Blakemore, Karin J.
Published in American journal of medical genetics. Part A (15.12.2004)
Published in American journal of medical genetics. Part A (15.12.2004)
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Isolation and characterization of the human gene encoding I to : further diversity by alternative mRNA splicing
Kong, Wei, Po, Sunny, Yamagishi, Toshio, Ashen, M Dominique, Stetten, Gail, Tomaselli, Gordon F
Published in American journal of physiology. Heart and circulatory physiology (01.12.1998)
Published in American journal of physiology. Heart and circulatory physiology (01.12.1998)
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