Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Zhi-ya Dong"'
Autor:
Juan-juan Zhang, Jun-qi Wang, Xu Xu, Li-dan Zhang, Cai-ping Zhang, Wen-li Lu, Wei-qiong Gu, Zhi-ya Dong, Yuan Xiao, Zhen-wei Xia
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
IntroductionThe frequency of celiac disease autoantibody (CDAb) positivity in type 1 diabetes (T1D) has increased due to unclear mechanisms, including autoimmune injury. Circular ribonucleic acids (circRNAs) participate in autoimmune diseases, but th
Externí odkaz:
https://doaj.org/article/f669d4923ab44e788ca2599c00e3902d
Publikováno v:
Neuroscience Letters. 256:5-8
Low density lipoprotein receptor related protein (LRP) is a receptor for protease complexes, and may function in cell growth and repair, and in tumor invasiveness. LRP expression increases in glioblastomas compared to lower grade astrocytomas. Two po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f86101863305212611b05e18bcb5b779
https://doi.org/10.1016/s0304-3940(98)00734-4
https://doi.org/10.1016/s0304-3940(98)00734-4
Autor:
Guo-ying, Chang, Zhi-ya, Dong, Wei, Wang, Yuan, Xiao, Feng-sheng, Chen, Ji-hong, Ni, Rui-fang, Wang, De-fen, Wang
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 49(6)
To analyze clinical characteristics of children with 45, X/46, XY mosaicism and explore effective managements for them.Five children with 45, X/46, XY mosaicism were all in puberty period, of whom, three were female and two male. The standing height,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4eeef397041fc7d55b90d4dd6177e2c
https://pubmed.ncbi.nlm.nih.gov/21924060
https://pubmed.ncbi.nlm.nih.gov/21924060
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 48(12)
To elucidate the curative and adverse effect of recombinant human growth hormone (rhGH) in 2 patients with isolated-growth hormone deficiency type IA (IGHDIA), to track sexual development and pregnancy, and reassess the quality of life in the adultho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c43996a3e1f7402f9e7a4c492e54fa43
https://pubmed.ncbi.nlm.nih.gov/21215191
https://pubmed.ncbi.nlm.nih.gov/21215191
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 47(10)
To detect CYP17A1 gene mutation in a patient with 17 alpha-hydroxylase/17, 20-lyase deficiency and her family members.Genomic DNA was extracted from the blood of the patient, her parents and twin sister. The 8 exons of CYP17A1 gene were amplified wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7afd9b5ff532937f4382aab6a89eb32c
https://pubmed.ncbi.nlm.nih.gov/20021817
https://pubmed.ncbi.nlm.nih.gov/20021817
Publikováno v:
Movement Disorders. 14:839-841
The C766T polymorphism in exon 3 of the low-density lipoprotein receptor-related protein (LRP) gene is underrepresented in Alzheimer's disease (AD) compared with normal subjects. We examined this polymorphism in 186 patients with Parkinson's disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f239423d8ff4dd8139593fe17946ebd
https://doi.org/10.1002/1531-8257(199909)14:5<839::aid-mds1019>3.0.co
https://doi.org/10.1002/1531-8257(199909)14:5<839::aid-mds1019>3.0.co
Autor:
Yuan, Xiao, Jun, Yang, Hui-jie, Zhang, Wei, Wang, Xiao-ying, Li, De-fen, Wang, Zhi-ya, Dong, Xiu-min, Wang
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 45(12)
Inactivating mutations of DAX-1 give rise to the X-linked form of adrenal hypoplasia congenita (AHC). Affected individuals are at risk of early postnatal Addisonian crisis, but the variable phenotypic expression of DAX-1 insufficiency renders this di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5540ab6ee7de02b9e71a0d4a6812bd38
https://pubmed.ncbi.nlm.nih.gov/18339285
https://pubmed.ncbi.nlm.nih.gov/18339285
Autor:
Wei, Wang, De-fen, Wang, Yi-fen, Cui, Ji-hong, Ni, Zhi-ya, Dong, Man-fen, Fu, Hong-mei, Fu, Guo-qiang, Lu, Feng-sheng, Chen
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 41(6)
Prader-Willi syndrome (PWS) is an example of a human genetic disorder that involves imprinting genes on the proximal long arm of chromosome 15 and SNRPN gene as a candidate gene for this syndrome. The purpose of this study was to show the molecular g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03e65d1bbac3c5091a7e8f91062e56d9
https://pubmed.ncbi.nlm.nih.gov/14749005
https://pubmed.ncbi.nlm.nih.gov/14749005