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Results: 1-15 |
Results: 15
Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease
Authors: MacDonald, TJ Brown, KM LaFleur, B Peterson, K Lawlor, C Chen, YD Packer, RJ Cogen, P Stephan, DA
Citation: Tj. Macdonald et al., Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease, NAT GENET, 29(2), 2001, pp. 143-152
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
Authors: Tiso, N Stephan, DA Nava, A Bagattin, A Devaney, JM Stanchi, F Larderet, G Brahmbhatt, B Brown, K Bauce, B Muriago, M Basso, C Thiene, G Danieli, GA Rampazzo, A
Citation: N. Tiso et al., Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2), HUM MOL GEN, 10(3), 2001, pp. 189-194
Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus
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
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15
Authors: Chen, AH Stephan, DA Hasson, T Fukushima, K Nelissen, CM Chen, AF Jun, AI Ramesh, A Van Camp, G Smith, RJH
Citation: Ah. Chen et al., MYO1F as a candidate gene for nonsyndromic deafness, DFNB15, ARCH OTOLAR, 127(8), 2001, pp. 921-925
Identification and characterization of a novel transcript of the murine growth hormone receptor gene exhibiting development and tissue-specific expression
Authors: Menon, RK Shaufl, A Yu, JH Stephan, DA Friday, RP
Citation: Rk. Menon et al., Identification and characterization of a novel transcript of the murine growth hormone receptor gene exhibiting development and tissue-specific expression, MOL C ENDOC, 172(1-2), 2001, pp. 135-146
Severe autosomal recessive rippling muscle disease
Authors: Koul, RL Chand, RP Chacko, A Ali, M Brown, KM Bushnarmuth, SR Escolar, DM Stephan, DA
Citation: Rl. Koul et al., Severe autosomal recessive rippling muscle disease, MUSCLE NERV, 24(11), 2001, pp. 1542-1547
Grtp1, a novel gene regulated by growth hormone
Authors: Lu, CX Kasik, J Stephan, DA Yang, SH Sperling, MA Menon, RK
Citation: Cx. Lu et al., Grtp1, a novel gene regulated by growth hormone, ENDOCRINOL, 142(10), 2001, pp. 4568-4571
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
Authors: Laitinen, PJ Brown, KM Piippo, K Swam, H Devaney, JM Brahmbhatt, B Donarum, EA Marino, M Tiso, N Viitasalo, M Toivonen, L Stephan, DA Kontula, K
Citation: Pj. Laitinen et al., Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia, CIRCULATION, 103(4), 2001, pp. 485-490
Positional cloning utilizing genomic DNA microarrays: The Niemann-Pick type C gene as a model system
Authors: Stephan, DA Chen, YD Jiang, Y Malechek, L Gu, JZ Robbins, CM Bittner, ML Morris, JA Carstea, E Meltzer, PS Adler, K Garlick, R Trent, JM Ashlock, MA
Citation: Da. Stephan et al., Positional cloning utilizing genomic DNA microarrays: The Niemann-Pick type C gene as a model system, MOL GEN MET, 70(1), 2000, pp. 10-18
Identification of tumor-suppressor genes using human melanoma cell lines UACC903, UACC903(+6), and SRS3 by comparison of expression profiles
Authors: Su, YA Bittner, ML Chen, YD Tao, L Jiang, Y Zhang, YH Stephan, DA Trent, JM
Citation: Ya. Su et al., Identification of tumor-suppressor genes using human melanoma cell lines UACC903, UACC903(+6), and SRS3 by comparison of expression profiles, MOL CARCINO, 28(2), 2000, pp. 119-127
A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region
Authors: Carpten, JD Makalowska, I Robbins, CM Scott, N Sood, R Connors, TD Bonner, TI Smith, JR Faruque, MU Stephan, DA Pinkett, H Morgenbesser, SD Su, K Graham, C Gregory, SG Williams, H McDonald, L Baxevanis, AD Klingler, KW Landes, GM Trent, JM
Citation: Jd. Carpten et al., A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region, GENOMICS, 64(1), 2000, pp. 1-14
The human RGL (RalGDS-like) gene: cloning, expression analysis and genomicorganization
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
Identification, chromosomal mapping, and partial characterization of mouseInsl6: A new member of the insulin family
Authors: Kasik, J Muglia, L Stephan, DA Menon, RK
Citation: J. Kasik et al., Identification, chromosomal mapping, and partial characterization of mouseInsl6: A new member of the insulin family, ENDOCRINOL, 141(1), 2000, pp. 458-461
Physical mapping of the rippling muscle disease locus
Authors: Stephan, DA Hoffman, EP
Citation: Da. Stephan et Ep. Hoffman, Physical mapping of the rippling muscle disease locus, GENOMICS, 55(3), 1999, pp. 268-274
Progressive juvenile-onset punctate cataracts caused by mutation of the gamma D-crystallin gene
Authors: Stephan, DA Gillanders, E Vanderveen, D Freas-Lutz, D Wistow, G Baxevanis, AD Robbins, CM VanAuken, A Quesenberry, MI Bailey-Wilson, J Juo, SHH Trent, JM Smith, L Brownstein, MJ
Citation: Da. Stephan et al., Progressive juvenile-onset punctate cataracts caused by mutation of the gamma D-crystallin gene, P NAS US, 96(3), 1999, pp. 1008-1012
Risultati: 1-15 |