Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Sing‐Wai Wong"'
Publikováno v:
ACS Omega, Vol 3, Iss 3, Pp 3592-3598 (2018)
Externí odkaz:
https://doaj.org/article/c00ec7ec6c0944239515db6083829bd5
Autor:
Jinglei Zheng, Haochen Liu, Yuan Zhan, Yang Liu, Sing‐Wai Wong, Tao Cai, Hailan Feng, Dong Han
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background Ectrodactyly‐Ectodermal dysplasia‐Cleft lip/palate (EEC) syndrome and Ankyloblepharon‐Ectodermal defects‐Cleft lip/palate (AEC) syndrome belong to p63 syndromes, a group of rare disorders exhibiting a wide variety of clini
Externí odkaz:
https://doaj.org/article/f526f4478e254972b25c3a1bc9f66374
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
The skin is a highly organized first line of defense that stretches up to 1.8 m2 and is home to more than a million commensal bacteria. The microenvironment of skin is driven by factors such as pH, temperature, moisture, sebum level, oxidative stress
Externí odkaz:
https://doaj.org/article/5ab24d8a67a244528b7e837c6892ff1f
Autor:
Xiangxiang Hu, Sing-Wai Wong, Kaixin Liang, Tai-Hsien Wu, Sheng Wang, Lufei Wang, Jie Liu, Mitsuo Yamauchi, Brian L. Foster, Jenny P.-Y. Ting, Baohong Zhao, Henry C. Tseng, Ching-Chang Ko
Publikováno v:
Science Advances. 9
Degenerative diseases affecting the nervous and skeletal systems affect the health of millions of elderly people. Optineurin (OPTN) has been associated with numerous neurodegenerative diseases and Paget’s disease of bone (PDB), a degenerative bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7a615c76a6cef11c53f2735f7a88660
https://doi.org/10.1126/sciadv.ade6998
https://doi.org/10.1126/sciadv.ade6998
Autor:
Vinícius de Paiva Gonçalves, Marta Liliana Musskopf, Angeliz Rivera-Concepcion, Christina Yu, Sing Wai Wong, Stephen A. Tuin, Yizu Jiao, Cristiano Susin, Luís Carlos Spolidorio, Patricia Almeida Miguez
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 13; Pages: 7100
This study aimed to evaluate the effects of hesperidin (HE) on in vitro osteoclastogenesis and dietary supplementation on mouse periodontal disease and femoral bone phenotype. RAW 264.7 cells were stimulated with RANKL in the presence or absence of H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8e163ecc371b087b842edd09bb0f8ec
https://pubmed.ncbi.nlm.nih.gov/35806105
https://pubmed.ncbi.nlm.nih.gov/35806105
Autor:
Kai Sun, Heng Liu, Miao Yu, Zhuangzhuang Fan, Liutao Zhang, Sing-Wai Wong, Yupeng Liu, Dong Han, Hailan Feng
Publikováno v:
Journal of Dental Research. 100:415-422
Genes associated with the WNT pathway play an important role in the etiology of tooth agenesis. Low-density lipoprotein receptor–related protein 6 encoding gene ( LRP6) is a recently defined gene that is associated with autosomal dominant inherited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cefc525cbe606867ecfe00c2a5e12049
https://doi.org/10.1177/0022034520970459
https://doi.org/10.1177/0022034520970459
Autor:
Tao Cai, Miao Yu, Hong Qu, Liutao Zhang, Jinglei Zheng, Yang Liu, Dong Han, Yongsheng Zhou, Haochen Liu, Hailan Feng, Sing-Wai Wong, Zhuangzhuang Fan
Publikováno v:
Human Mutation. 41:1957-1966
Nonsyndromic oligodontia is a rare congenital anomaly. Mutations in the ectodysplasin A receptor (EDAR) gene are the primary cause of hypohidrotic ectodermal dysplasia but are rarely reported in nonsyndromic oligodontia. This study investigated EDAR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02f2114ac973dad1f2e501100658ce12
https://doi.org/10.1002/humu.24104
https://doi.org/10.1002/humu.24104
Autor:
Hailan Feng, Heng Liu, Yupeng Liu, Sing-Wai Wong, Jinguang Wu, Dong Han, Miao Yu, Yangyuan Wang
Publikováno v:
Journal of Dental Research. 99:311-319
WNT10A (Wingless-type MMTV integration site family, member 10A) plays a crucial role in tooth development, and patients with biallelic WNT10A mutation and mice lacking Wnt10a show taurodontism. However, whether epithelial or mesenchymal WNT10A contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faf07ab85d71bca449da45d3dbb09558
https://doi.org/10.1177/0022034519897607
https://doi.org/10.1177/0022034519897607
Autor:
Li Zeng, Sing-Wai Wong, Hailan Feng, Yang Liu, Hong Qu, Dong Han, Fang Li, Miao Yu, Haochen Liu, Shichen Sun
Publikováno v:
Archives of Oral Biology. 101:100-107
Objective: To explore the gene mutation in an incontinentia pigmenti (IP) patient with syndromic tooth agenesis. Methods: Long-range polymerase chain reaction (PCR) and Sanger sequencing were used to detect inhibitor of nuclear factor kappa-B kinase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::037041680abfd46c29acab4f313f22cf
https://doi.org/10.1016/j.archoralbio.2019.03.013
https://doi.org/10.1016/j.archoralbio.2019.03.013
Publikováno v:
Non-Canonical Autophagy ISBN: 9780128205389
Since its first description as a catabolic, survival mechanisms in 1963, our understanding and appreciation of autophagy has grown exponentially. No longer considered solely a nonselective recycling and degradation system triggered by nutrient depriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e01835a369757e968706c5818521b0f2
https://doi.org/10.1016/b978-0-12-820538-9.00005-3
https://doi.org/10.1016/b978-0-12-820538-9.00005-3
