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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 13, 2006
[Progresses and perspectives in the study on citrin deficiency]
Yao-bang Lu, Fei Peng, Meng-xian Li, et al.
Journal of Human Genetics
|
April 9, 2008
Identification of 13 novel mutations including a retrotransposal insertion in SLC25A13 gene and frequency of 30 mutations found in patients with citrin deficiency
Ayako Tabata, Jian-Sheng Sheng, Miharu Ushikai, et al.
Molecular Genetics and Metabolism
|
March 31, 2004
Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle
Takeyori Saheki, Keiko Kobayashi, Mikio Iijima, et al.
Molecular Genetics and Metabolism
|
December 19, 2003
Screening of nine SLC25A13 mutations: their frequency in patients with citrin deficiency and high carrier rates in Asian populations
Keiko Kobayashi, Yao Bang Lu, Meng Xian Li, et al.
Neuroscience Research
|
March 17, 2006
Fasting-induced reduction in locomotor activity and reduced response of orexin neurons in carnitine-deficient mice
Goichiro Yoshida, Meng Xian Li, Masahisa Horiuchi, et al.
Molecular Genetics and Metabolism
|
November 16, 2004
Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients
Yusaku Tazawa, Keiko Kobayashi, Daiki Abukawa, et al.
Journal of Human Genetics
|
August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency
Yao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 13, 2006
[Progresses and perspectives in the study on citrin deficiency]
Yao-bang Lu, Fei Peng, Meng-xian Li, et al.
Journal of Human Genetics
|
April 9, 2008
Identification of 13 novel mutations including a retrotransposal insertion in SLC25A13 gene and frequency of 30 mutations found in patients with citrin deficiency
Ayako Tabata, Jian-Sheng Sheng, Miharu Ushikai, et al.
Molecular Genetics and Metabolism
|
March 31, 2004
Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle
Takeyori Saheki, Keiko Kobayashi, Mikio Iijima, et al.
Molecular Genetics and Metabolism
|
December 19, 2003
Screening of nine SLC25A13 mutations: their frequency in patients with citrin deficiency and high carrier rates in Asian populations
Keiko Kobayashi, Yao Bang Lu, Meng Xian Li, et al.
Neuroscience Research
|
March 17, 2006
Fasting-induced reduction in locomotor activity and reduced response of orexin neurons in carnitine-deficient mice
Goichiro Yoshida, Meng Xian Li, Masahisa Horiuchi, et al.
Molecular Genetics and Metabolism
|
November 16, 2004
Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients
Yusaku Tazawa, Keiko Kobayashi, Daiki Abukawa, et al.
Journal of Human Genetics
|
August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency
Yao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.
Page
of 1