HKU Scholars Hub: Browsing DSpace

Browsing by Author Scherer, SW

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 53 to 72 of 110 < previous next >

Title	Author(s)	Issue Date	Views
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas Journal:Oncogene	Edelson, MI Scherer, SW Tsui, LC Welch, WR Bell, DA Berkowitz, RS Mok, SC	1997	190
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome Journal:Genomics	Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC	1999
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient Journal:American Journal of Human Genetics	Alley, TL Gray, BA Lee, SH Scherer, SW Tsui, LC Tint, GS Williams, CA Zori, R Wallace, MR	1995	100
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients Journal:Genomics	Osborne, LR Martindale, D Scherer, SW Shi, XM Huizenga, J Heng, HHQ Costa, T Pober, B Lew, L Brinkman, J Rommens, J Koop, B Tsui, LC	1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Journal:Nature genetics	Belloni, E Muenke, M Roessler, E Traverso, G SiegelBartelt, J Frumkin, A Mitchell, HF DonisKeller, H Helms, C Hing, AV Heng, HH Koop, B Martindale, D Rommens, JM Tsui, LC Scherer, SW	1996	222
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31 Journal:Genomics	Cheung, J Petek, E Nakabayashi, K Tsui, LC Vincent, JB Scherer, SW	2001
Involvement of the HLXB9 homeobox gene in Currarino syndrome [2] Journal:American Journal of Human Genetics	Belloni, E Martucciello, G Verderio, D Ponti, E Seri, M Jasonni, V Torre, M Ferrari, M Tsui, LC Scherer, SW	2000	221
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism Journal:Cell	Sattterstrom, FK Kosmicki, JA Wang, J Breen, MS De Rubeis, S An, JY Peng, M Collins, R Grove, J Klei, L Stevens, C Pedersen, CB Pedersen, MG Poterba, T Poulsen, JB Ripke, S Schork, AJ Thompson, WK Turley, P Walters, RK Brand, H Montenegro, EMS Schwartz, G Nguyen, R Guerrero, EE Dias, C Betancur, C Cook, EH Gallagher, L Gill, M Sutcliffe, JS Thurm, A Moreira, D Zwick, ME Borglum, AD State, MW Cicek, AE Talkowski, ME Cutler, DJ Devlin, B Sanders, SJ Roeder, K Daly, MJ Morrow, EM Buxbaum, JD Aleksic, B Anney, R Barbosa, M Bishop, S Brusco, A Bybjerg-Grauholm, J Carracedo, A Chan, MCY Chiocchetti, AG Mors, O Chung, BHY Coon, H Cuccaro, ML Curro, A Dalla Bernardina, B Doan, R Domenici, E Dong, S Fallerini, C Fernandez-Prieto, M Mortensen, PB Ferrero, GM Freitag, CM Fromer, M Gargus, JJ Geschwind, D Giorgio, E Gonzalez-Perias, J Guter, S Halpern, D Hansen-Kiss, E Mosconi, M He, X Herman, GE Hertz-Piccfiotto, I Hougaard, DM Hultman, CM Ionita-Laza, L Jacob, S Jamison, J Jugessur, A Kaartinen, M Muglia, P Knudsen, GP Kolevzon, A Kushima, I Lee, SL Lehtimaki, T Lim, ET Lintas, C Lipkin, WI Lopergolo, D Lopes, F Neale, BM Ludena, Y Maciel, P Magnus, P Mahjani, B Maltman, N Manoach, DS Meiri, G Menashe, I Miller, J Minshew, N Nordentoft, M Ozaki, N Reichert, J Palotie, A Parellada, M Passos-Bueno, MR Pericak-Vance, M Persico, AM Pessah, I Puura, K Reichenberg, A Renien, A Riberi, E Mulhern, MS Robinson, EB Samocha, KE Sandin, S Santangelo, SI Schellenberg, G Scherer, SW Schlitt, S Schmidt, R Schmitt, L Silva, IMW Artomov, M Singh, T Siper, PM Smith, M Soares, G Stoltenberg, C Suren, P Susser, E Sweeney, J Szatmari, P Tang, L Gerges, S Tassone, F Teufel, K Trabetti, E Trelles, MDP Walsh, CA Weiss, LA Werge, T Werling, DM Wigdor, EM Wilkinson, E Sheppard, S Willsey, AJ Yu, TW YU, HC Yuen, R Zachi, E Agerbo, E Als, TD Appadurai, V Baekvad-Hansen, M Belliveau, R Xu, X Buil, A Carey, CE Cerrato, F Chambert, K Churchhouse, C Dalsgaard, S Demontis, D Dumont, A Goldstein, J Hansen, CS Bhaduri, A Hauberg, ME Hollegaard, MV Howrigan, DP Huang, H Maller, J Martin, AR Martin, J Mattheisen, M Moran, J Pallesen, J Norman, U Palmer, DS	2020	80
Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1 Journal:Genomics	Torigoe, K Harada, T Kusaba, H Uchiumi, T Kohno, K Green, ED Scherer, SW Tsui, LC Schlessinger, D Kuwano, M Wada, M	1998
Localization of the gene encoding the α 2/δ-subunits of the L-type voltage dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families Journal:Human Molecular Genetics	Iles, DE LehmannHorn, F Scherer, SW Tsui, LC Weghuis, DO Suijkerbuijk, RF Heytens, L Mikala, G Schwartz, A Ellis, FR Stewart, AD Deufel, T Wieringa, B	1994	183
Localization of the gene encoding the α2/δ subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21- q22 by somatic cell hybrid analysis Journal:Genomics	Powers, PA Scherer, SW Tsui, LC Gregg, RG Hogan, K	1994
Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31→q32 Journal:Cytogenetics and Cell Genetics	Scherer, SW Otulakowski, G Robinson, BH Tsui, LC	1991	162
Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q Journal:Genomics	Scherer, SW Duvoisin, RM Kuhn, R Heng, HHQ Belloni, E Tsui, LC	1996
Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents Journal:Human Molecular Genetics	Thacker, J Tambini, CE Simpson, PJ Tsui, LC Scherer, SW	1995	188
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas Journal:Oncogene	Zeng, WR Scherer, SW Koutsilieris, M Huizenga, JJ Filteau, F Tsui, LC Nepveu, A	1997	161
MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinoma Journal:Cell	Eppert, K Scherer, SW Ozcelik, H Pirone, R Hoodless, P Kim, H Tsui, LC Bapat, B Gallinger, S Andrulis, IL Thomsen, GH Wrana, JL Attisano, L	1996	186
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12 Journal:Genomics	Egan, S Herbrick, JA Tsui, LC Cohen, B Flock, G Beatty, B Scherer, SW	1998
Mapping the midkine family of developmentally regulated signaling molecules Journal:Mammalian Genome	Peichel, CL Scherer, SW Tsui, LC Beier, DR Vogt, TF	1993
Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre) Journal:Human Molecular Genetics	Coyle, B Reardon, W Herbrick, JA Tsui, LC Gausden, E Lee, J Coffey, R Grueters, A Grossman, A Phelps, PD Luxon, L KendallTaylor, P Scherer, SW Trembath, RC	1998
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site Journal:Proceedings of the National Academy of Sciences of the United States of America	Mishmar, D Rahat, A Scherer, SW Nyakatura, G Hinzmann, B Kohwi, Y MandelGutfroind, Y Lee, JR Drescher, B Sas, DE Margalit, H Platzer, M Weiss, A Tsui, LC Rosenthal, A Kerem, B	1998	133

Showing results 53 to 72 of 110 < previous next >