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Refinado por: Nome da Publicação: Human Molecular Genetics remover assunto: Molecular And Cellular Biology remover
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1
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
Leucine-rich repeat kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease
Leucine-rich repeat kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease
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Leucine-rich repeat kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease

Venderova, Katerina ; Kabbach, Ghassan ; Abdel-Messih, Elizabeth ; Zhang, Yi ; Parks, Robin J. ; Imai, Yuzuru ; Gehrke, Stephan ; Ngsee, Johnny ; LaVoie, Matthew J. ; Slack, Ruth S. ; Rao, Yong ; Zhang, Zhuohua ; Lu, Bingwei ; Haque, M. Emdadul ; Park, David S.

Human molecular genetics, 2009-11, Vol.18 (22), p.4390-4404 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
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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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
ELF1 is associated with systemic lupus erythematosus in Asian populations
ELF1 is associated with systemic lupus erythematosus in Asian populations
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ELF1 is associated with systemic lupus erythematosus in Asian populations

JING YANG ; WANLING YANG ; KA WING LEE ; SIK NIN WONG ; LEUNG, Alexander Moon Ho ; LI, Xiang-Pei ; AVIHINGSANON, Yingyos ; RIANTHAVORN, Pornpimol ; DEEKAJORNDEJ, Thavatchai ; SUPHAPEETIPORN, Kanya ; SHOTELERSUK, Vorasuk ; BAUM, Larry ; HIRANKARN, Nattiya ; KWAN, Patrick ; TSZ LEUNG LEE ; HOK KUNG HO, Marco ; PUI WAH LEE, Pamela ; HING SANG WONG, Wilfred ; SHUAI ZENG ; JING ZHANG ; WONG, Chun-Ming ; OI LIN NG, Irene ; GARCIA-BARCELO, Maria-Mercè ; DONG QING YE ; CHERNY, Stacey S ; KWONG-HANG TAM, Paul ; PAK CHUNG SHAM ; CHAK SING LAU ; YU LUNG LAU ; YAN ZHANG ; PAN, Hai-Feng ; CHI CHIU MOK ; TAK MAO CHAN ; WONG, Raymond Woon Sing ; MO YIN MOK

Human molecular genetics, 2011-02, Vol.20 (3), p.601-607 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
A set of miRNAs that involve in the pathways of drug resistance and leukemic stem-cell differentiation is associated with the risk of relapse and glucocorticoid response in childhood ALL
A set of miRNAs that involve in the pathways of drug resistance and leukemic stem-cell differentiation is associated with the risk of relapse and glucocorticoid response in childhood ALL
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A set of miRNAs that involve in the pathways of drug resistance and leukemic stem-cell differentiation is associated with the risk of relapse and glucocorticoid response in childhood ALL

Han, Bo-Wei ; Feng, Dan-Dan ; Li, Zhi-Gang ; Luo, Xue-Qun ; Zhang, Hua ; Li, Xiao-Juan ; Zhang, Xing-Ju ; Zheng, Ling-Ling ; Zeng, Cheng-Wu ; Lin, Kang-Yu ; Zhang, Peng ; Xu, Ling ; Chen, Yue-Qin

Human molecular genetics, 2011-12, Vol.20 (24), p.4903-4915 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies
Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies
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Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies

Sun, Bo Wen ; Yang, A. Cong ; Feng, Yun ; Sun, Yi Juan ; Zhu, Yu fei ; Zhang, Yi ; Jiang, Hua ; Li, Chun Liang ; Gao, Fu Rong ; Zhang, Zhi Hong ; Wang, Wei Cheng ; Kong, Xiang Yin ; Jin, Gang ; Fu, Shi Jun ; Jin, Ying

Human molecular genetics, 2006-01, Vol.15 (1), p.65-75 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes
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Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes

Li, Wen ; Wang, Xianming ; Fan, Wenxia ; Zhao, Ping ; Chan, Yau-Chi ; Chen, Shen ; Zhang, Shiqiang ; Guo, Xiangpeng ; Zhang, Ya ; Li, Yanhua ; Cai, Jinglei ; Qin, Dajiang ; Li, Xingyan ; Yang, Jiayin ; Peng, Tianran ; Zychlinski, Daniela ; Hoffmann, Dirk ; Zhang, Ruosi ; Deng, Kang ; Ng, Kwong-Man ; Menten, Bjorn ; Zhong, Mei ; Wu, Jiayan ; Li, Zhiyuan ; Chen, Yonglong ; Schambach, Axel ; Tse, Hung-Fat ; Pei, Duanqing ; Esteban, Miguel A

Human molecular genetics, 2012-01, Vol.21 (1), p.32-45 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus
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A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

Orrú, Valeria ; Tsai, Sophia J. ; Rueda, Blanca ; Fiorillo, Edoardo ; Stanford, Stephanie M. ; Dasgupta, Jhimli ; Hartiala, Jaana ; Zhao, Lei ; Ortego-Centeno, Norberto ; D’Alfonso, Sandra ; Arnett, Frank C. ; Wu, Hui ; Gonzalez-Gay, Miguel A. ; Tsao, Betty P. ; Pons-Estel, Bernardo ; Alarcon-Riquelme, Marta E. ; He, Yantao ; Zhang, Zhong-Yin ; Allayee, Hooman ; Chen, Xiaojiang S. ; Martin, Javier ; Bottini, Nunzio

Human molecular genetics, 2009-02, Vol.18 (3), p.569-579 [Periódico revisado por pares]

Oxford: Oxford University Press

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