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Results: 1-20 |
Results: 20
VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domain
Authors: Tseng, TC Marfatia, SM Bryant, PJ Pack, S Zhuang, ZP O'Brien, JE Lin, LH Hanada, T Chishti, AH
Citation: Tc. Tseng et al., VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domain, BBA-GENE ST, 1518(3), 2001, pp. 249-259
Intramedullary Ewing sarcoma of the spinal cord: consequences of moleculardiagnostics - Case report
Authors: Weil, RJ Zhuang, ZP Pack, S Kumar, S Helman, L Fuller, BG Mackall, CL Oldfield, EH
Citation: Rj. Weil et al., Intramedullary Ewing sarcoma of the spinal cord: consequences of moleculardiagnostics - Case report, J NEUROSURG, 95(2), 2001, pp. 270-275
Reassignment of the EPB4 center dot 1 gene to 1p36 and assessment of its involvement in neuroblastomas
Authors: Huang, S Lichtenauer, UD Pack, S Wang, C Kim, AC Lutchman, M Koch, CA Torres-Cruz, J Huang, SC Benz, EJ Christiansen, H Dockhorn-Dworniczak, B Poremba, C Vortmeyer, AO Chishti, AH Zhuang, Z
Citation: S. Huang et al., Reassignment of the EPB4 center dot 1 gene to 1p36 and assessment of its involvement in neuroblastomas, EUR J CL IN, 31(10), 2001, pp. 907-914
Amplification of 4q21-q22 and the MXR gene in independently entry derived mitoxantrone-resistant cell lines
Authors: Knutsen, T Rao, VK Ried, T Mickley, L Schneider, E Miyake, K Ghadimi, BM Padilla-Nash, H Pack, S Greenberger, L Cowan, K Dean, M Fojo, T Bates, S
Citation: T. Knutsen et al., Amplification of 4q21-q22 and the MXR gene in independently entry derived mitoxantrone-resistant cell lines, GENE CHROM, 27(1), 2000, pp. 110-116
Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis
Authors: Reginster, JY Minne, HW Sorensen, OH Hooper, M Roux, C Brandi, ML Lund, B Ethgen, D Pack, S Roumagnac, I Eastell, R
Citation: Jy. Reginster et al., Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis, OSTEOPOR IN, 11(1), 2000, pp. 83-91
A pooled data analysis on the use of intermittent cyclical etidronate therapy for the prevention and treatment of corticosteroid induced bone loss
Authors: Adachi, JD Roux, C Pitt, PI Cooper, C Moniz, C Dequeker, J Ioannidis, G Cawley, MID Jenkins, EA Walker-Bone, KE Pack, S Stephenson, GF Laan, RF Brown, J Geusens, P
Citation: Jd. Adachi et al., A pooled data analysis on the use of intermittent cyclical etidronate therapy for the prevention and treatment of corticosteroid induced bone loss, J RHEUMATOL, 27(10), 2000, pp. 2424-2431
VHL gene inactivation in an endolymphatic sac tumor associated with von Hippel-Lindau disease
Authors: Vortmeyer, AO Choo, D Pack, S Oldfield, E Zhuang, ZP
Citation: Ao. Vortmeyer et al., VHL gene inactivation in an endolymphatic sac tumor associated with von Hippel-Lindau disease, NEUROLOGY, 55(3), 2000, pp. 460-460
Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy
Authors: Stratakis, CA Papageorgiou, T Premkumar, A Pack, S Kirschner, LS Taymans, SE Zhuang, ZP Oelkers, WH Carney, JA
Citation: Ca. Stratakis et al., Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy, J CLIN END, 85(11), 2000, pp. 4359-4366
Morbidly obese patients with pulmonary disease - A retrospective study of four cases - A brief report
Authors: Guernelli, J Wainapel, SF Pack, S Miranda-Lama, E
Citation: J. Guernelli et al., Morbidly obese patients with pulmonary disease - A retrospective study of four cases - A brief report, AM J PHYS M, 78(1), 1999, pp. 60-65
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes
Authors: Kirschner, LS Taymans, SE Pack, S Pak, E Pike, BL Chandrasekharappa, SC Zhuang, ZP Stratakis, CA
Citation: Ls. Kirschner et al., Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes, GENOMICS, 62(1), 1999, pp. 21-33
Allelic loss of 11q13 as detected by MEN1-FISH is not associated with mutation of the MEN1 gene in lymphoid neoplasms
Authors: Thieblemont, C Pack, S Sakai, A Beaty, M Pak, E Vortmeyer, AO Wellmann, A Zhuang, Z Jaffe, ES Raffeld, M
Citation: C. Thieblemont et al., Allelic loss of 11q13 as detected by MEN1-FISH is not associated with mutation of the MEN1 gene in lymphoid neoplasms, LEUKEMIA, 13(1), 1999, pp. 85-91
The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: Genetic and physical VDR map
Authors: Taymans, SE Pack, S Pak, E Orban, Z Barsony, J Zhuang, ZP Stratakis, CA
Citation: Se. Taymans et al., The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: Genetic and physical VDR map, J BONE MIN, 14(7), 1999, pp. 1163-1166
Loss of heterozygosity on 8p in prostate cancer implicates a role for dematin in tumor progression
Authors: Lutchman, M Pack, S Kim, AC Azim, A Emmert-Buck, M van Huffel, C Zhuang, ZP Chishti, AH
Citation: M. Lutchman et al., Loss of heterozygosity on 8p in prostate cancer implicates a role for dematin in tumor progression, CANC GENET, 115(1), 1999, pp. 65-69
CALL gene is haploinsufficient in a 3p-syndrome patient
Authors: Angeloni, D Lindor, NM Pack, S Latif, F Wei, MH Lerman, MI
Citation: D. Angeloni et al., CALL gene is haploinsufficient in a 3p-syndrome patient, AM J MED G, 86(5), 1999, pp. 482-485
Detection of EWS-FLI-1 fusion in Ewing's sarcoma peripheral primitive neuroectodermal tumor by fluorescence in situ hybridization using formalin-fixed paraffin-embedded tissue
Authors: Kumar, S Pack, S Kumar, D Walker, R Quezado, M Zhuang, ZP Meltzer, P Tsokos, M
Citation: S. Kumar et al., Detection of EWS-FLI-1 fusion in Ewing's sarcoma peripheral primitive neuroectodermal tumor by fluorescence in situ hybridization using formalin-fixed paraffin-embedded tissue, HUMAN PATH, 30(3), 1999, pp. 324-330
Absence of EWS/FLI1 fusion in olfactory neuroblastomas indicates these tumors do not belong to the Ewing's sarcoma family
Authors: Kumar, S Perlman, E Pack, S Davis, M Zhang, H Meltzer, P Tsokos, M
Citation: S. Kumar et al., Absence of EWS/FLI1 fusion in olfactory neuroblastomas indicates these tumors do not belong to the Ewing's sarcoma family, HUMAN PATH, 30(11), 1999, pp. 1356-1360
Nuclear/cytoplasmic localization of the multiple endocrine neoplasia type 1 gene product, menin
Authors: Huang, SC Zhuang, ZP Weil, RJ Pack, S Wang, CY Krutzsch, HC Pham, TA Lubensky, IA
Citation: Sc. Huang et al., Nuclear/cytoplasmic localization of the multiple endocrine neoplasia type 1 gene product, menin, LAB INV, 79(3), 1999, pp. 301-310
Somatic mutations in the kinase domain of the MET/hepatocyte growth factorreceptor gene in childhood hepatocellular carcinomas
Authors: Park, WS Dong, SM Kim, SY Na, EY Shin, MS Pi, JH Kim, BJ Bae, JH Hong, YK Lee, KS Lee, SH Yoo, NJ Jang, JJ Pack, S Zhuang, ZP Schmidt, L Zbar, B Lee, JY
Citation: Ws. Park et al., Somatic mutations in the kinase domain of the MET/hepatocyte growth factorreceptor gene in childhood hepatocellular carcinomas, CANCER RES, 59(2), 1999, pp. 307-310
Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype
Authors: Lubensky, IA Schmidt, L Zhuang, ZP Weirich, G Pack, S Zambrano, N Walther, MM Choyke, P Linehan, WM Zbar, B
Citation: Ia. Lubensky et al., Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype, AM J PATH, 155(2), 1999, pp. 517-526
Translocation of chromosomes 11 and 22 in choroidal metastatic Ewing sarcoma detected by fluorescent in situ hybridization
Authors: Chan, CC Pack, S Pak, E Tsogos, M Zhuang, Z
Citation: Cc. Chan et al., Translocation of chromosomes 11 and 22 in choroidal metastatic Ewing sarcoma detected by fluorescent in situ hybridization, AM J OPHTH, 127(2), 1999, pp. 226-228
Risultati: 1-20 |