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21.
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[Clinical and molecular genetic analysis for 7 patients from 5 pedigrees with 17a-hydroxylase/17, 20 lyase deficiency]. [electronic resource] by
- Liu, Bing-li
- Qiao, Jie
- Chen, Xia
- Liang, Jun
- Zuo, Chun-lin
- Gu, Yan-yun
- Han, Bing
- Gong, Jing
- Ru, Ying
- Lu, Ying-li
- Wu, Wan-ling
- Chen, Ming-dao
- Song, Huai-dong
Producer: 20090917
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 26
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22.
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A Lon-like protease with no ATP-powered unfolding activity. [electronic resource] by
- Liao, Jiahn-Haur
- Kuo, Chiao-I
- Huang, Ya-Yi
- Lin, Yu-Ching
- Lin, Yen-Chen
- Yang, Chen-Yui
- Wu, Wan-Ling
- Chang, Wei-Hau
- Liaw, Yen-Chywan
- Lin, Li-Hua
- Chang, Chung-I
- Wu, Shih-Hsiung
Producer: 20130319
In:
PloS one vol. 7
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23.
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A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency. [electronic resource] by
- Qiao, Jie
- Han, Bing
- Liu, Bing-Li
- Liu, Wei
- Wu, Jia-Jun
- Pan, Chun-Ming
- Jiang, He
- Gu, Ting
- Jiang, Bo-Ren
- Zhu, Hui
- Lu, Ying-Li
- Wu, Wan-Ling
- Chen, Ming-Dao
- Song, Huai-Dong
Producer: 20110606
In:
European journal of endocrinology vol. 164
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24.
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Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency. [electronic resource] by
- Qiao, Jie
- Chen, Xia
- Zuo, Chun-Lin
- Gu, Yan-Yun
- Liu, Bing-Li
- Liang, Jun
- Lu, Ying-Li
- Tang, Jin-Feng
- Wu, Yi-Xin
- Chen, Ming-Dao
- Chen, Jia-Lun
- Wu, Wan-Ling
- Song, Huai-Dong
Producer: 20100701
In:
Clinical endocrinology vol. 72
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25.
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Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor. [electronic resource] by
- Han, Bing
- Wang, Zhi-quan
- Xue, Li-qiong
- Ma, Jun-hua
- Liu, Wei
- Liu, Bing-li
- Wu, Jia-jun
- Pan, Chun-ming
- Chen, Xia
- Zhao, Shuang-xia
- Lu, Ying-li
- Wu, Wan-ling
- Qiao, Jie
- Song, Huai-dong
Producer: 20120703
In:
Molecular human reproduction vol. 18
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26.
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Identifying a novel mutation of CYP17A1 gene from five Chinese 17α-hydroxylase/17, 20-lyase deficiency patients. [electronic resource] by
- Han, Bing
- Liu, Wei
- Zuo, Chun-Lin
- Zhu, Hui
- Li, Lu
- Xu, Chao
- Wang, Xia-Juan
- Liu, Bing-Li
- Pan, Chun-Ming
- Lu, Ying-Li
- Wu, Wan-Ling
- Chen, Ming-Dao
- Song, Huai-Dong
- Cheng, Kai-Xiang
- Qiao, Jie
Producer: 20130329
In:
Gene vol. 516
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27.
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A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism. [electronic resource] by
- Qiao, Jie
- Han, Bing
- Liu, Bing-Li
- Chen, Xia
- Ru, Ying
- Cheng, Kai-Xiang
- Chen, Fu-Guo
- Zhao, Shuang-Xia
- Liang, Jun
- Lu, Ying-Li
- Tang, Jin-Feng
- Wu, Yi-Xin
- Wu, Wan-Ling
- Chen, Jia-Lun
- Chen, Ming-Dao
- Song, Huai-Dong
Producer: 20091117
In:
Human mutation vol. 30
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28.
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Acetylome of [electronic resource] by
- Liao, Jiahn-Haur
- Tsai, Cheng-Han
- Patel, Sanjay G
- Yang, Jhih-Tian
- Tu, I-Fan
- Lo Cicero, Matteo
- Lipka-Lloyd, Magdalena
- Wu, Wan-Ling
- Shen, Wen-Jie
- Ho, Meng-Ru
- Chou, Chi-Chi
- Sharma, Garima R
- Okanishi, Hiroki
- Luk, Louis Y P
- Tsai, Yu-Hsuan
- Wu, Shih-Hsiung
Publication details: Frontiers in molecular biosciences 2017
In:
Frontiers in molecular biosciences vol. 4
Availability: No items available.
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