Zobrazeno 1 - 4
of 4
pro vyhledávání: '"S J, Clapcote"'
Autor:
Igor Vukobradovic, G. Xie, J. G. Sled, J. Rossant, Lucy R. Osborne, Jeffrey T. Henderson, S. J. Clapcote, S. P. Cordes, T. Tallerico, John C. Roder, Y. Huang, B. J. Nieman
Publikováno v:
Genes, Brain and Behavior. 6:717-727
Dominant mutations of the P/Q-type Ca(2+) channel (CACNA1A) underlie several human neurological disorders, including episodic ataxia type 2, familial hemiplegic migraine 1 (FHM1) and spinocerebellar ataxia 6, but have not been found previously in the
Autor:
J, Dachtler, J, Glasper, R N, Cohen, J L, Ivorra, D J, Swiffen, A J, Jackson, M K, Harte, R J, Rodgers, S J, Clapcote
Publikováno v:
Translational Psychiatry
Autism is a common and frequently disabling neurodevelopmental disorder with a strong genetic basis. Human genetic studies have discovered mutations disrupting exons of the NRXN2 gene, which encodes the synaptic adhesion protein α-neurexin II (Nrxn2
Autor:
S M Brown, S J Clapcote, J K Millar, H S Torrance, S M Anderson, R Walker, A Rampino, J C Roder, P A Thomson, D J Porteous, K L Evans
Publikováno v:
Molecular Psychiatry. 17:469-469
Autor:
Allison R. Bechard, Sandra Carattini-Rivera, Tao Yu, Annie Pao, Y. Eugene Yu, John C. Roder, Zhongyou Li, William C. Mobley, Steven J. Clapcote, Chunhong Liu, Antonio Baldini, Sei Ichi Matsui, Allan Bradley
Publikováno v:
Mammalian genome
21 (2010): 258–267. doi:10.1007/s00335-010-9262-x
info:cnr-pdr/source/autori:Yu T(1,2); Clapcote SJ(3); Li Z(1,2); Liu C(1,2); Pao A(1,2); Bechard AR(4); Carattini-Rivera S(5); Matsui S(1,2); Roder JC(4); Baldini A(6); Mobley WC(7); Bradley A(8); Yu YE(1,2)/titolo:Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice./doi:10.1007%2Fs00335-010-9262-x/rivista:Mammalian genome (Print)/anno:2010/pagina_da:258/pagina_a:267/intervallo_pagine:258–267/volume:21
21 (2010): 258–267. doi:10.1007/s00335-010-9262-x
info:cnr-pdr/source/autori:Yu T(1,2); Clapcote SJ(3); Li Z(1,2); Liu C(1,2); Pao A(1,2); Bechard AR(4); Carattini-Rivera S(5); Matsui S(1,2); Roder JC(4); Baldini A(6); Mobley WC(7); Bradley A(8); Yu YE(1,2)/titolo:Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice./doi:10.1007%2Fs00335-010-9262-x/rivista:Mammalian genome (Print)/anno:2010/pagina_da:258/pagina_a:267/intervallo_pagine:258–267/volume:21
Copy-number variation in the human genome can be disease-causing or phenotypically neutral. This type of genetic rearrangement associated with human chromosome 21 (Hsa21) underlies partial Monosomy 21 and Trisomy 21. Mental retardation is a major cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f2822e24bf895285203c3dc01b1265