Publisher： Oxford University Press
Founded in： 1992
Total resources： 344
E-ISSN： 1460-2083
ISSN： 1460-2083
Subject： R5 Internal Medicine
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Human Molecular Genetics
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A patient-derived olfactory stem cell disease model for ataxia-telangiectasia
By Stewart Romal,Kozlov Sergei,Matigian Nicholas,Wali Gautam,Gatei Magtouf,Sutharsan Ratneswary,Bellette Bernadette,Wraith-Kijas Amanda,Cochrane Julie,Coulthard Mark,Perry Chris,Sinclair Kate,Mackay-Sim Alan,Lavin Martin F. in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.
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PINK1 and Parkin complementarily protect dopaminergic neurons in vertebrates
By Matsui Hideaki,Gavinio Roberto,Asano Takeshi,Uemura Norihito,Ito Hidefumi,Taniguchi Yoshihito,Kobayashi Yoshito,Maki Takakuni,Shen Jie,Takeda Shunichi,Uemura Kengo,Yamakado Hodaka,Takahashi Ryosuke in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.By Tamura Masaru,Hosoya Masaki,Fujita Motoi,Iida Tomoko,Amano Takanori,Maeno Akiteru,Kataoka Taro,Otsuka Taketo,Tanaka Shigekazu,Tomizawa Shuichi,Shiroishi Toshihiko in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.Gata3 antagonizes cancer progression in Pten -deficient prostates
By Nguyen Alana H.T.,Tremblay Mathieu,Haigh Katharina,Koumakpayi Ismaël Hervé,Paquet Marilène,Pandolfi Pier Paolo,Mes-Masson Anne-Marie,Saad Fred,Haigh Jody J.,Bouchard Maxime in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis
By Kabashi Edor,El Oussini Hajer,Bercier Valérie,Gros-Louis François,Valdmanis Paul N.,McDearmid Jonathan,Mejier Inge A.,Dion Patrick A.,Dupre Nicolas,Hollinger David,Sinniger Jérome,Dirrig-Grosch Sylvie,Camu William,Meininger Vincent,Loeffler Jean-Philippe,René Frédérique,Drapeau Pierre,Rouleau Guy A.,Dupuis Luc in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.Pathogenic NPHP5 mutations impair protein interaction with Cep290, a prerequisite for ciliogenesis
By Barbelanne Marine,Song Jenny,Ahmadzai Mustafa,Tsang William Y. in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.By Roos Sara,Macao Bertil,Fusté Javier Miralles,Lindberg Christopher,Jemt Elisabeth,Holme Elisabeth,Moslemi Ali-Reza,Oldfors Anders,Falkenberg Maria in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrest
By Nizialek Emily A.,Peterson Charissa,Mester Jessica L.,Downes-Kelly Erinn,Eng Charis in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.By Jiang Mali,Peng Qi,Liu Xia,Jin Jing,Hou Zhipeng,Zhang Jiangyang,Mori Susumu,Ross Christopher A.,Ye Keqiang,Duan Wenzhen in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.Developmental abnormalities in mouse embryos lacking the HDL receptor SR-BI
By Santander Nicolás Guillermo,Contreras-Duarte Susana,Awad Marı´a Fernanda,Lizama Carlos,Passalacqua Isabella,Rigotti Attilio,Busso Dolores in (2013)
Human Molecular Genetics , Vol. 22, Iss. 12, 2013-06 , pp.
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