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Refinado por: Nome da Publicação: Human Molecular Genetics remover assunto: Mice remover
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Calpain and STriatal-Enriched protein tyrosine Phosphatase (STEP) activation contribute to extrasynaptic NMDA receptor localization in a Huntington's disease mouse model
Calpain and STriatal-Enriched protein tyrosine Phosphatase (STEP) activation contribute to extrasynaptic NMDA receptor localization in a Huntington's disease mouse model
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Calpain and STriatal-Enriched protein tyrosine Phosphatase (STEP) activation contribute to extrasynaptic NMDA receptor localization in a Huntington's disease mouse model

GLADDING, Clare M ; SEPERS, Marja D ; JIAN XU ; ZHANG, Lily Y. J ; MILNERWOOD, Austen J ; LOMBROSO, Paul J ; RAYMOND, Lynn A

Human molecular genetics, 2012-09, Vol.21 (17), p.3739-3752 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice
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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

Puckelwartz, Megan J. ; Kessler, Eric ; Zhang, Yuan ; Hodzic, Didier ; Randles, K. Natalie ; Morris, Glenn ; Earley, Judy U. ; Hadhazy, Michele ; Holaska, James M. ; Mewborn, Stephanie K. ; Pytel, Peter ; McNally, Elizabeth M.

Human molecular genetics, 2009-02, Vol.18 (4), p.607-620 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Rac1 mediates the osteoclast gains-in-function induced by haploinsufficiency of Nf1
Rac1 mediates the osteoclast gains-in-function induced by haploinsufficiency of Nf1
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Rac1 mediates the osteoclast gains-in-function induced by haploinsufficiency of Nf1

Yan, Jincheng ; Chen, Shi ; Zhang, Yingze ; Li, Xiaohong ; Li, Yan ; Wu, Xiaohua ; Yuan, Jin ; Robling, Alexander G. ; Karpur, Reuben ; Chan, Rebecca J. ; Yang, Feng-Chun

Human molecular genetics, 2008-04, Vol.17 (7), p.936-948 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
A Genome-Wide Screen for Asthma-Associated Quantitative Trait Loci in a Mouse Model of Allergic Asthma
A Genome-Wide Screen for Asthma-Associated Quantitative Trait Loci in a Mouse Model of Allergic Asthma
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A Genome-Wide Screen for Asthma-Associated Quantitative Trait Loci in a Mouse Model of Allergic Asthma

Zhang, Youming ; Lefort, Jean ; Kearsey, Virginia ; Lapa e Silva, José Roberto ; Cookson, William O. C. M. ; Vargaftig, B. Boris

Human molecular genetics, 1999-04, Vol.8 (4), p.601-605 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Suppression of Ca2+ signaling in a mouse model of Best disease
Suppression of Ca2+ signaling in a mouse model of Best disease
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Suppression of Ca2+ signaling in a mouse model of Best disease

Zhang, Youwen ; Stanton, J. Brett ; Wu, Jiang ; Yu, Kuai ; Hartzell, H. Criss ; Peachey, Neal S. ; Marmorstein, Lihua Y. ; Marmorstein, Alan D.

Human molecular genetics, 2010-03, Vol.19 (6), p.1108-1118 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia
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Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia

Du, Wei ; Tao, Ye ; Deng, Wen-Tao ; Zhu, Ping ; Li, Jie ; Dai, Xufeng ; Zhang, Yuxin ; Shi, Wei ; Liu, Xuan ; Chiodo, Vince A ; Ding, Xi-Qin ; Zhao, Chen ; Michalakis, Stylianos ; Biel, Martin ; Zhang, Zuoming ; Qu, Jia ; Hauswirth, William W ; Pang, Ji-Jing

Human molecular genetics, 2015-07, Vol.24 (13), p.3699-3707 [Periódico revisado por pares]

England: Oxford University Press

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7
Age and insertion site dependence of repeat number instability of a human DM1 transgene in individual mouse sperm
Age and insertion site dependence of repeat number instability of a human DM1 transgene in individual mouse sperm
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Age and insertion site dependence of repeat number instability of a human DM1 transgene in individual mouse sperm

Zhang, Yun ; Monckton, Darren G. ; Siciliano, Michael J. ; Connor, Thomas H. ; Meistrich, Marvin L.

Human molecular genetics, 2002-04, Vol.11 (7), p.791-798 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Human skeletal muscle xenograft as a new preclinical model for muscle disorders
Human skeletal muscle xenograft as a new preclinical model for muscle disorders
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Human skeletal muscle xenograft as a new preclinical model for muscle disorders

Zhang, Yuanfan ; King, Oliver D ; Rahimov, Fedik ; Jones, Takako I ; Ward, Christopher W ; Kerr, Jaclyn P ; Liu, Naili ; Emerson, Jr, Charles P ; Kunkel, Louis M ; Partridge, Terence A ; Wagner, Kathryn R

Human molecular genetics, 2014-06, Vol.23 (12), p.3180-3188 [Periódico revisado por pares]

England: Oxford University Press

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9
Cloning and Characterization of a Secreted Frizzled-Related Protein that is Expressed by the Retinal Pigment Epithelium
Cloning and Characterization of a Secreted Frizzled-Related Protein that is Expressed by the Retinal Pigment Epithelium
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Cloning and Characterization of a Secreted Frizzled-Related Protein that is Expressed by the Retinal Pigment Epithelium

Chang, Jinghua T. ; Esumi, Noriko ; Moore, Kathryn ; Li, Yuanyuan ; Zhang, Suiyuan ; Chew, Christina ; Goodman, Barbara ; Rattner, Amir ; Moody, Sally ; Stetten, Gail ; Campochiaro, Peter A. ; Zack, Donald J.

Human molecular genetics, 1999-04, Vol.8 (4), p.575-583 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice
Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice
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Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice

POULADI, Mahmoud A ; STANEK, Lisa M ; HAYDEN, Michael R ; YUANYUN XIE ; FRANCIOSI, Sonia ; SOUTHWELL, Amber L ; YU DENG ; BUTLAND, Stefanie ; WEINING ZHANG ; CHENG, Seng H ; SHIHABUDDIN, Lamya S

Human molecular genetics, 2012-05, Vol.21 (10), p.2219-2232 [Periódico revisado por pares]

Oxford: Oxford University Press

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