Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Zhonglin Jia"'
Autor:
Shiyu Chen, Zhonglin Jia, Ming Cai, Mujie Ye, Dandan Wu, Teng Wan, Bowen Zhang, Peixuan Wu, Yuexin Xu, Yuntao Guo, Chan Tian, Duan Ma, Jing Ma
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Non-syndromic cleft lip and palate (NSCLP) is one of the most common congenital malformations with multifactorial etiology. Although long non-coding RNAs (lncRNAs) have been implicated in the development of lip and palate, their roles in NSCLP are no
Externí odkaz:
https://doaj.org/article/203e1d5edb344a16a97c728e221cc62e
Autor:
Lulin Huang, Zhonglin Jia, Yi Shi, Qin Du, Jiayu Shi, Ziyan Wang, Yandong Mou, Qingwei Wang, Bihe Zhang, Qing Wang, Shi Ma, He Lin, Shijun Duan, Bin Yin, Yansong Lin, Yiru Wang, Dan Jiang, Fang Hao, Lin Zhang, Haixin Wang, Suyuan Jiang, Huijuan Xu, Chengwei Yang, Chenghao Li, Jingtao Li, Bing Shi, Zhenglin Yang
Publikováno v:
PLoS Genetics, Vol 15, Iss 10, p e1008357 (2019)
Nonsyndromic orofacial cleft (NSOFC) is a severe birth defect that occurs early in embryonic development and includes the subtypes cleft palate only (CPO), cleft lip only (CLO) and cleft lip with cleft palate (CLP). Given a lack of specific genetic f
Externí odkaz:
https://doaj.org/article/c1e71e270a1c416fb244477b65a1032c
Autor:
Zena T Wolf, Elizabeth J Leslie, Boaz Arzi, Kartika Jayashankar, Nili Karmi, Zhonglin Jia, Douglas J Rowland, Amy Young, Noa Safra, Saundra Sliskovic, Jeffrey C Murray, Claire M Wade, Danika L Bannasch
Publikováno v:
PLoS Genetics, Vol 10, Iss 4, p e1004257 (2014)
Cleft palate (CP) is one of the most commonly occurring craniofacial birth defects in humans. In order to study cleft palate in a naturally occurring model system, we utilized the Nova Scotia Duck Tolling Retriever (NSDTR) dog breed. Micro-computed t
Externí odkaz:
https://doaj.org/article/3c8a3673c2594cea8fff240da57ea38e
Autor:
Yanlian Xiong, Yaru Si, Rengui Quan, Xingyu Huo, Juntong Chen, Jinyu Xu, Zhonglin Jiang, Feibo Xu, Ranran Liu, Qiang Fu
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Premature ovarian insufficiency (POI), a major cause of female infertility, is defined as follicular atresia and a rapid loss of germ cells in women of reproductive age due to ovarian failure. Recently, findings from several studies have ind
Externí odkaz:
https://doaj.org/article/c9dce9e1b40f4f8b806a28f5c48cf6e5
Publikováno v:
Oral Diseases.
A significant genetic association between rs7078160 in VAX1 and NSCL/P has been established through genome-wide association studies (GWAS), and we previously replicated the association in the Chinese population. The critical issue in the post-GWAS er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d23881da05f5f86cf8350458c7bde90
https://doi.org/10.1111/odi.14210
https://doi.org/10.1111/odi.14210
Autor:
Xu Cheng, Jiayu Shi, Zhonglin Jia, Pin Ha, Chia Soo, Kang Ting, Aaron W. James, Bing Shi, Xinli Zhang
Publikováno v:
Am J Pathol
The American journal of pathology, vol 192, iss 3
The American journal of pathology, vol 192, iss 3
Neural epidermal growth factor-like (EGFL)-like protein (NELL)-1 is a potent and key osteogenic factor in the development and regeneration of skeletal tissues. Intriguingly, accumulative data from genome-wide association studies (GWASs) have started
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de763dfc15ada1959cd66ac7e7410c54
https://europepmc.org/articles/PMC8895422/
https://europepmc.org/articles/PMC8895422/
Autor:
null Sidi Zhang, null Qianming Chen, null Chao Yang, null Jiayu Shi, null Yansong Lin, null Shijun Duan, null Bing Shi, null Zhonglin Jia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b332d90e333e9ec67150cea6d7b63939
https://doi.org/10.1111/odi.14100/v3/response1
https://doi.org/10.1111/odi.14100/v3/response1
Autor:
Sidi Zhang, Qianming Chen, Chao Yang, Jiayu Shi, Yansong Lin, Shijun Duan, Bing Shi, Zhonglin Jia
Publikováno v:
Oral diseasesREFERENCES.
Considering limitations of previous studies and differences across populations and subtypes, this study aimed to identify new potential SNPs around IRF6 associated with non-syndromic orofacial cleft (NSOC) in Western Han Chinese.We recruited 376 NSOC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a21d76799f810038e5fb43f886ed38
https://pubmed.ncbi.nlm.nih.gov/34894020
https://pubmed.ncbi.nlm.nih.gov/34894020
Autor:
null Siyue Wang, null Jiayu Shi, null Chunfang Liu, null Ping Wang, null Mengying Wang, null Wenyong Li, null Ren Zhou, null Hongchen Zheng, null Jin Jiang, null Nan Li, null Jing Li, null Zhibo Zhou, null Hongping Zhu, null Yiqun Wu, null Zhonglin Jia, null Tao Wu, null Yonghua Hu, null Terri H. Beaty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23e6a05c86503398881f80c503a765d2
https://doi.org/10.1111/odi.14068/v3/response1
https://doi.org/10.1111/odi.14068/v3/response1
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562211253
Objective The role of MMP16 in lip development is unclear. This study aimed to identify nonsyndromic cleft lip with or without palate (NSCL ± P) susceptible loci of MMP16 in western Han Chinese. Design We performed targeted sequencing around MMP16 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71137d060d64e2f663ccb10c0a7f2072
https://doi.org/10.1177/10556656221125392
https://doi.org/10.1177/10556656221125392