Reduced Chrna7 expression in mice is associated with decreases in hippocampal markers of inhibitory function: implications for neuropsychiatric diseases
Adams, C.E, Yonchek, J.C, Schulz, K.M, Graw, S.L, Stitzel, J, Teschke, P.U, Stevens, K.E
Published in Neuroscience (05.04.2012)
Published in Neuroscience (05.04.2012)
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Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects
GIGLIO, S, GRAW, S. L, DIGILIO, M. C, GIANNOTTI, A, MARINO, B, CARROZZO, R, KORENBERG, J. R, DANESINO, C, SUJANSKY, E, DALLAPICCOLA, B, ZUFFARDI, O, GIMELLI, G, PIROLA, B, VARONE, P, VOULLAIRE, L, LERZO, F, ROSSI, E, DELLAVECCHIA, C, BONAGLIA, M. C
Published in Circulation (New York, N.Y.) (25.07.2000)
Published in Circulation (New York, N.Y.) (25.07.2000)
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Genetic and physical map of the interferon region on chromosome 9p
Fountain, Jane W., Karayiorgou, Maria, Taruscio, Domenica, Graw, Sharon L., Buckler, Alan J., Ward, David C., Dracopoli, Nicholas C., Housman, David E.
Published in Genomics (San Diego, Calif.) (01.09.1992)
Published in Genomics (San Diego, Calif.) (01.09.1992)
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Identification of germline 185delAG BRCA1 mutations in non‐Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado
Mullineaux, Lisa G., Castellano, Teresa M., Shaw, Jeffrey, Axell, Lisen, Wood, Marie E., Diab, Sami, Klein, Catherine, Sitarik, Mark, Deffenbaugh, Amie M., Graw, Sharon L.
Published in Cancer (01.08.2003)
Published in Cancer (01.08.2003)
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Identification of human chromosome 9 specific genes using exon amplification
Church, D M, Banks, L T, Rogers, A C, Graw, S L, Housman, D E, Gusella, J F, Buckler, A J
Published in Human molecular genetics (01.11.1993)
Published in Human molecular genetics (01.11.1993)
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Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome
Jackson, C L, Britt, D E, Graw, S L, Potts, A, Santoro, K, Buckler, A J, Housman, D E, Mark, H F
Published in Somatic cell and molecular genetics (01.05.1992)
Published in Somatic cell and molecular genetics (01.05.1992)
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Generation and characterization of a human chromosome 9 cosmid library
Graw, S L, Buckler, A J, Britt, D E, Jackson, C L, Taruscio, D, Baldini, A, Ward, D C, Housman, D E
Published in Somatic cell and molecular genetics (01.05.1992)
Published in Somatic cell and molecular genetics (01.05.1992)
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Cosmid assembly and anchoring to human chromosome 21
Soeda, Eiichi, Hou, De-Xing, Osoegawa, Kazutoyo, Atsuchi, Yasuo, Yamagata, Tetsushi, Shimokawa, Takanori, Kishida, Haruo, Soeda, Emiko, Okano, Saishi, Chumakov, Ilya, Cohen, Daniel, Raff, Malcolm, Gardiner, Katheleen, Graw, Sharon L., Patterson, David, De Jong, Pieter, Ashworth, Linda K., Slezak, Tom, Carrano, Anthony V.
Published in Genomics (San Diego, Calif.) (1995)
Published in Genomics (San Diego, Calif.) (1995)
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Purification of mammalian glycinamide ribonucleotide (GAR) synthetase
Hards, R G, Graw, S L, Patterson, D
Published in Advances in experimental medicine and biology (1986)
Published in Advances in experimental medicine and biology (1986)
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α-myosin heavy chain : A sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy
CARNIEL, Elisa, TAYLOR, Matthew R. G, GRAW, Sharon L, FEIGER, Jennie, XIAO ZHONG ZHU, DAO, Dmi, FERGUSON, Debra A, BRISTOW, Michael R, MESTRONI, Luisa, SINAGRA, Gianfranco, DI LENARDA, Andrea, KU, Lisa, FAIN, Pamela R, BOUCEK, Mark M, CAVANAUGH, Mi Jean, MIOCIC, Snjezana, SLAVOV, Dobromir
Published in Circulation (New York, N.Y.) (05.07.2005)
Published in Circulation (New York, N.Y.) (05.07.2005)
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Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy
Taylor, Matthew R.G., Slavov, Dobromir, Gajewski, Andreas, Vlcek, Sylvia, Ku, Lisa, Fain, Pamela R., Carniel, Elisa, Di Lenarda, Andrea, Sinagra, Gianfranco, Boucek, Mark M., Cavanaugh, Jean, Graw, Sharon L., Ruegg, Patsy, Feiger, Jennie, Zhu, Xiao, Ferguson, Debra A., Bristow, Michael R., Gotzmann, Josef, Foisner, Roland, Mestroni, Luisa
Published in Human mutation (01.12.2005)
Published in Human mutation (01.12.2005)
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