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Refinado por: Nome da Publicação: Human Molecular Genetics remover
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41
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population
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An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Sun, Pengfei ; Zhou, Wei ; Fu, Yi ; Cheung, Chloe Y Y ; Dong, Yujun ; Yang, Min-Lee ; Zhang, He ; Jia, Jia ; Huo, Yong ; Willer, Cristen J ; Chen, Y Eugene ; Tang, Clara S ; Tse, Hung-Fat ; Lam, Karen S L ; Gao, Wei ; Xu, Ming ; Yu, Haiyi ; Sham, Pak Chung ; Zhang, Yan ; Ganesh, Santhi K

Human molecular genetics, 2021-05, Vol.30 (9), p.836-842 [Periódico revisado por pares]

England: Oxford University Press

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42
Impact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulation
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Impact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulation

Zhang, Xinjun ; Lin, Hai ; Zhao, Huiying ; Hao, Yangyang ; Mort, Matthew ; Cooper, David N ; Zhou, Yaoqi ; Liu, Yunlong

Human molecular genetics, 2014-06, Vol.23 (11), p.3024-3034 [Periódico revisado por pares]

England: Oxford University Press

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43
Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration
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Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration

Zhang, Zhongjian ; Lee, Yi-Ching ; Kim, Sung-Jo ; Choi, Moonsuk S. ; Tsai, Pei-Chih ; Saha, Arjun ; Wei, Hui ; Xu, Yan ; Xiao, Yi-Jin ; Zhang, Peng ; Heffer, Alison ; Mukherjee, Anil B.

Human molecular genetics, 2007-04, Vol.16 (7), p.837-847 [Periódico revisado por pares]

Oxford: Oxford University Press

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44
Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL
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Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL

Zhang, Zhongjian ; Lee, Yi-Ching ; Kim, Sung-Jo ; Choi, Moonsuk S. ; Tsai, Pei-Chih ; Xu, Yan ; Xiao, Yi-Jin ; Zhang, Peng ; Heffer, Alison ; Mukherjee, Anil B.

Human molecular genetics, 2006-01, Vol.15 (2), p.337-346 [Periódico revisado por pares]

Oxford: Oxford University Press

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45
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching
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Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

Carvalho, Claudia M.B. ; Zhang, Feng ; Liu, Pengfei ; Patel, Ankita ; Sahoo, Trilochan ; Bacino, Carlos A. ; Shaw, Chad ; Peacock, Sandra ; Pursley, Amber ; Tavyev, Y. Jane ; Ramocki, Melissa B. ; Nawara, Magdalena ; Obersztyn, Ewa ; Vianna-Morgante, Angela M. ; Stankiewicz, Pawel ; Zoghbi, Huda Y. ; Cheung, Sau Wai ; Lupski, James R.

Human molecular genetics, 2009-06, Vol.18 (12), p.2188-2203 [Periódico revisado por pares]

Oxford: Oxford University Press

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46
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
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Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium

Cai, Qiuyin ; Long, Jirong ; Lu, Wei ; Qu, Shimian ; Wen, Wanqing ; Kang, Daehee ; Lee, Ji-Young ; Chen, Kexin ; Shen, Hongbing ; Shen, Chen-Yang ; Sung, Hyuna ; Matsuo, Keitaro ; Haiman, Christopher A ; Khoo, Ui Soon ; Ren, Zefang ; Iwasaki, Motoki ; Gu, Kai ; Xiang, Yong-Bing ; Choi, Ji-Yeob ; Park, Sue K ; Zhang, Lina ; Hu, Zhibin ; Wu, Pei-Ei ; Noh, Dong-Young ; Tajima, Kazuo ; Henderson, Brian E ; Chan, Kelvin Y.K ; Su, Fengxi ; Kasuga, Yoshio ; Wang, Wenjing ; Cheng, Jia-Rong ; Yoo, Keun-Young ; Lee, Jong-Young ; Zheng, Hong ; Liu, Yao ; Shieh, Ya-Lan ; Kim, Sung-Won ; Lee, Jong Won ; Iwata, Hiroji ; Le Marchand, Loic ; Chan, Sum Yin ; Xie, Xiaoming ; Tsugane, Shoichiro ; Lee, Min Hyuk ; Wang, Shenming ; Li, Guoliang ; Levy, Shawn ; Huang, Bo ; Shi, Jiajun ; Delahanty, Ryan ; Zheng, Ying ; Li, Chun ; Gao, Yu-Tang ; Shu, Xiao-Ou ; Zheng, Wei

Human molecular genetics, 2011-12, Vol.20 (24), p.4991-4999 [Periódico revisado por pares]

Oxford: Oxford University Press

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47
Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case–control study
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Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case–control study

Calton, Melissa A. ; Ersoy, Baran A. ; Zhang, Sumei ; Kane, John P. ; Malloy, Mary J. ; Pullinger, Clive R. ; Bromberg, Yana ; Pennacchio, Len A. ; Dent, Robert ; McPherson, Ruth ; Ahituv, Nadav ; Vaisse, Christian

Human molecular genetics, 2009-03, Vol.18 (6), p.1140-1147 [Periódico revisado por pares]

Oxford: Oxford University Press

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48
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk
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Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk

Chang, Bao-Li ; Cramer, Scott D. ; Wiklund, Fredrik ; Isaacs, Sarah D. ; Stevens, Victoria L. ; Sun, Jielin ; Smith, Shelly ; Pruett, Kristen ; Romero, Lina M. ; Wiley, Kathleen E. ; Kim, Seong-Tae ; Zhu, Yi ; Zhang, Zheng ; Hsu, Fang-Chi ; Turner, Aubrey R. ; Adolfsson, Jan ; Liu, Wennuan ; Kim, Jin Woo ; Duggan, David ; Carpten, John ; Zheng, S. Lilly ; Rodriguez, Carmen ; Isaacs, William B. ; Grönberg, Henrik ; Xu, Jianfeng

Human molecular genetics, 2009-04, Vol.18 (7), p.1368-1375 [Periódico revisado por pares]

Oxford: Oxford University Press

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49
Genetic dissection of the Down syndrome critical region
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Genetic dissection of the Down syndrome critical region

Jiang, Xiaoling ; Liu, Chunhong ; Yu, Tao ; Zhang, Li ; Meng, Kai ; Xing, Zhuo ; Belichenko, Pavel V ; Kleschevnikov, Alexander M ; Pao, Annie ; Peresie, Jennifer ; Wie, Sarah ; Mobley, William C ; Yu, Y Eugene

Human molecular genetics, 2015-11, Vol.24 (22), p.6540-6551 [Periódico revisado por pares]

England: Oxford University Press

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50
The signaling pathways implicated in impairment of hepatic autophagy in glycogen storage disease type Ia
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The signaling pathways implicated in impairment of hepatic autophagy in glycogen storage disease type Ia

Gautam, Sudeep ; Zhang, Lisa ; Arnaoutova, Irina ; Lee, Cheol ; Mansfield, Brian C ; Chou, Janice Y

Human molecular genetics, 2020-03, Vol.29 (5), p.834-844 [Periódico revisado por pares]

England: Oxford University Press

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Deste Autor:

  1. Nawara, M
  2. Ramocki, M
  3. Liu, P
  4. Zhang, F
  5. Pursley, A

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