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Results: 1-8 |
Results: 8

Authors: Sood, R Bonner, TI Makalowska, I Stephan, DA Robbins, CM Connors, TD Morgenbesser, SD Su, K Faruque, MU Pinkett, H Graham, C Baxevanis, AD Klinger, KW Landes, GM Trent, JM Carpten, JD
Citation: R. Sood et al., Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus, GENOMICS, 73(2), 2001, pp. 211-222

Authors: Bianchi, DW Farina, A Weber, W Delli-Bovi, LC DeRiso, M Williams, JM Klinger, KW
Citation: Dw. Bianchi et al., Significant fetal-maternal hemorrhage after termination of pregnancy: Implications for development of fetal cell microchimerism, AM J OBST G, 184(4), 2001, pp. 703-706

Authors: Ibraghimov-Beskrovnaya, O Bukanov, NO Donohue, LC Dackowski, WR Klinger, KW Landes, GM
Citation: O. Ibraghimov-beskrovnaya et al., Strong homophilic interactions of the Ig-like domains of polycystin-1,the protein product of an autosomal dominant polycystic kidney disease gene, PKD1, HUM MOL GEN, 9(11), 2000, pp. 1641-1649

Authors: Sood, R Makalowska, I Carpten, JD Robbins, CM Stephan, DA Connors, TD Morgenbesser, SD Su, K Pinkett, HW Graham, CL Quesenberry, MI Baxevanis, AD Klinger, KW Trent, JM Bonner, TI
Citation: R. Sood et al., The human RGL (RalGDS-like) gene: cloning, expression analysis and genomicorganization, BBA-GENE ST, 1491(1-3), 2000, pp. 285-288

Authors: Klinger, KW Ibraghimov-Beskrovnaya, O
Citation: Kw. Klinger et O. Ibraghimov-beskrovnaya, Polycystins - Membrane-associated proteins involved in autosomal dominant polycystic kidney disease, MEMBRANE STRUCTURE IN DISEASE AND DRUG THERAPY, 2000, pp. 409-426

Authors: Haddow, JE Bradley, LA Palomaki, GE Doherty, RA Bernhardt, BA Brock, DJH Cheuvront, B Cunningham, GC Donnenfeld, AE Erickson, JL Erlick, HA Ferrie, RM FitzSimmons, SC Greene, MF Grody, WW Haddow, PK Harris, H Holmes, LB Howell, RR Katz, M Klinger, KW Kloza, EM LeFevre, ML Little, S Loeben, G McGovern, M Pyeritz, RE Rowley, PT Saiki, RK Short, MP Tabone, J Wald, NJ Wilker, NL Witt, DR
Citation: Je. Haddow et al., Issues in implementing prenatal screening for cystic fibrosis: Results of a working conference (vol 1, pg 129, 1999), GENET MED, 1(5), 1999, pp. 193-193

Authors: Haddow, JE Bradley, LA Palomaki, GE Doherty, RA Bernhardt, BA Brock, DJH Cheuvront, B Cunningham, GC Donnenfeld, AE Erickson, JL Erlich, HA Ferrie, RM FitzSimmons, SC Greene, MF Grody, WW Haddow, PK Harris, H Holmes, LB Howell, RR Katz, M Klinger, KW Kloza, EM LeFevre, ML Little, S Loeben, G McGovern, M Pyeritz, RE Rowley, PT Saiki, RK Short, MP Tabone, J Wald, NJ Wilker, NL Witt, DR
Citation: Je. Haddow et al., Issues in implementing prenatal screening for cystic fibrosis: Results of a working conference, GENET MED, 1(4), 1999, pp. 129-135

Authors: Watnick, T Phakdeekitcharoen, B Johnson, A Gandolph, M Wang, M Briefel, G Klinger, KW Kimberling, W Gabow, P Germino, GG
Citation: T. Watnick et al., Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease, AM J HU GEN, 65(6), 1999, pp. 1561-1571
Risultati: 1-8 |