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Results: 1-9 |
Results: 9
Functional annotation of a full-length mouse cDNA collection
Authors: Kawai, J Shinagawa, A Shibata, K Yoshino, M Itoh, M Ishii, Y Arakawa, T Hara, A Fukunishi, Y Konno, H Adachi, J Fukuda, S Aizawa, K Izawa, M Nishi, K Kiyosawa, H Kondo, S Yamanaka, I Saito, T Okazaki, Y Gojobori, T Bono, H Kasukawa, T Saito, R Kadota, K Matsuda, H Ashburner, M Batalov, S Casavant, T Fleischmann, W Gaasterland, T Gissi, C King, B Kochiwa, H Kuehl, P Lewis, S Matsuo, Y Nikaido, I Pesole, G Quackenbush, J Schriml, LM Staubli, F Suzuki, R Tomita, M Wagner, L Washio, T Sakai, K Okido, T Furuno, M Aono, H Baldarelli, R Barsh, G Blake, J Boffelli, D Bojunga, N Carninci, P de Bonaldo, MF Brownstein, MJ Bult, C Fletcher, C Fujita, M Gariboldi, M Gustincich, S Hill, D Hofmann, M Hume, DA Kamiya, M Lee, NH Lyons, P Marchionni, L Mashima, J Mazzarelli, J Mombaerts, P Nordone, P Ring, B Ringwald, M Rodriguez, I Sakamoto, N Sasaki, H Sato, K Schonbach, C Seya, T Shibata, Y Storch, KF Suzuki, H Toyo-oka, K Wang, KH Weitz, C Whittaker, C Wilming, L Wynshaw-Boris, A Yoshida, K Hasegawa, Y Kawaji, H Kohtsuki, S Hayashizaki, Y
Citation: J. Kawai et al., Functional annotation of a full-length mouse cDNA collection, NATURE, 409(6821), 2001, pp. 685-690
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase gene
Authors: Hahn, H Trant, MR Brownstein, MJ Harper, RA Milstien, S Butler, IJ
Citation: H. Hahn et al., Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase gene, ARCH NEUROL, 58(5), 2001, pp. 749-755
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia
Authors: Slaugenhaupt, SA Blumenfeld, A Gill, SP Leyne, M Mull, J Cuajungco, MP Liebert, CB Chadwick, B Idelson, M Reznik, L Robbins, CM Makalowska, I Brownstein, MJ Krappmann, D Scheidereit, C Maayan, C Axelrod, FB Gusella, JF
Citation: Sa. Slaugenhaupt et al., Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia, AM J HU GEN, 68(3), 2001, pp. 598-605
Alpha-synuclein immunoreactivity of huntingtin polyglutamine aggregates instriatum and cortex of Huntington's disease patients and transgenic mouse models
Authors: Charles, V Mezey, E Reddy, PH Dehejia, A Young, TA Polymeropoulos, MH Brownstein, MJ Tagle, DA
Citation: V. Charles et al., Alpha-synuclein immunoreactivity of huntingtin polyglutamine aggregates instriatum and cortex of Huntington's disease patients and transgenic mouse models, NEUROSCI L, 289(1), 2000, pp. 29-32
Isolation and characterization of the human homeobox gene HOX D1
Authors: Appukuttan, B Sood, R Ott, S Makalowska, I Patel, RJ Wang, XG Robbins, CM Brownstein, MJ Stout, JT
Citation: B. Appukuttan et al., Isolation and characterization of the human homeobox gene HOX D1, MOL BIOL RP, 27(4), 2000, pp. 195-201
Molecular cloning and functional characterization of a vasotocin receptor subtype that is expressed in the shell gland and brain of the domestic chicken
Authors: Tan, FI Lolait, SJ Brownstein, MJ Saito, N MacLeod, V Baeyens, DA Mayeux, PR Jones, SM Cornett, LE
Citation: Fi. Tan et al., Molecular cloning and functional characterization of a vasotocin receptor subtype that is expressed in the shell gland and brain of the domestic chicken, BIOL REPROD, 62(1), 2000, pp. 8-15
Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease (vol 3, pg 493, 1998)
Authors: Mezey, E Dehejia, AM Harta, G Tresser, N Suchy, SF Nussbaum, RL Brownstein, MJ Polymeropoulos, MH
Citation: E. Mezey et al., Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease (vol 3, pg 493, 1998), MOL PSYCHI, 4(2), 1999, pp. 197-197
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
Localization of a gene for Duane retraction syndrome to chromosome 2q31
Authors: Appukuttan, B Gillanders, E Juo, SH Freas-Lutz, D Ott, S Sood, R Van Auken, A Bailey-Wilson, J Wang, XG Patel, RJ Robbins, CM Chung, M Annett, G Weinberg, K Borchert, MS Trent, JM Brownstein, MJ Stout, JT
Citation: B. Appukuttan et al., Localization of a gene for Duane retraction syndrome to chromosome 2q31, AM J HU GEN, 65(6), 1999, pp. 1639-1646
Risultati: 1-9 |