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1 . Academic Journal
Identification of SERPINA1 promoting better prognosis in papillary thyroid carcinoma along with Hashimoto’s thyroiditis through WGCNA analysis
저자
by
Yihan Zhang
;
Xin Xie
;
Hong Zhou
;
Bingxin Li
;
Li Ding
, et al.
소스
Frontiers in Endocrinology, Vol 14 (2023)
Open Access (DOAJ)
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7 . Academic Journal
In‐frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance
저자
by
Wenjiao Zhu
;
Yuanping Shi
;
Changrun Zhang
;
Yajie Peng
;
Yueyue Wan
, et al.
소스
Clinical and Translational Medicine, Vol 13, Iss 1, Pp n/a-n/a (2023)
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7 . Academic Journal
Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants
저자
by
Hui Zhu
;
Haijun Yao
;
Yue Xu
;
Yan Chen
;
Bing Han
, et al.
소스
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
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7 . Academic Journal
Generation of two induced pluripotent stem cell lines, SHIPMi001-A from a patient with hypertrophic cardiomyopathy caused by MYBPC3 gene mutation and SHIPMi002-A from a healthy male individual
저자
by
Yue Wang
;
Weiyao Xiong
;
Shuangxia Zhao
;
Bin Li
;
Alex Chia Yu Chang
.
소스
Stem Cell Research, Vol 57, Iss , Pp 102594- (2021)
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7 . Academic Journal
Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique
저자
by
Hao Wang
;
Hui Zhu
;
Nan Wang
;
Tong Cheng
;
Bing Han
, et al.
소스
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
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7 . Academic Journal
Effects of Osteoglycin (OGN) on treating senile osteoporosis by regulating MSCs
저자
by
Xia Chen
;
Junsong Chen
;
Dongliang Xu
;
Shuangxia Zhao
;
Huaidong Song
, et al.
소스
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-10 (2017)
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7 . Academic Journal
Correlation of TSHR and CTLA-4 Single Nucleotide Polymorphisms with Graves Disease
저자
by
Weihua Sun
;
Xiaomei Zhang
;
Jing Wu
;
Wendi Zhao
;
Shuangxia Zhao
, et al.
소스
International Journal of Genomics, Vol 2019 (2019)
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7 . Academic Journal
Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population.
저자
by
Liqiong Xue
;
Chunming Pan
;
Zhaohui Gu
;
Shuangxia Zhao
;
Bing Han
, et al.
소스
PLoS ONE, Vol 8, Iss 12, p e84514 (2013)
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7 . Academic Journal
Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency.
저자
by
Yue Xu
;
Shutian Jiang
;
Zheng Yan
;
Yao Niu
;
Wenhua Du
, et al.
소스
Journal of Clinical Endocrinology & Metabolism; Jun2022, Vol. 107 Issue 6, pe2610-e2618, 9p
Full Text (OUP)
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7 .
PARD3
gene variation as candidate cause of nonsyndromic cleft palate only
저자
by
Renjie Cui
;
Dingli Chen
;
Na Li
;
Ming Cai
;
Teng Wan
, et al.
소스
Journal of Cellular and Molecular Medicine
. 26:4292-4304
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