Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Qining Xing"'
Autor:
Qining Xing, Wenjun Tian, Lin Wang, Zhongqing Zhao, Shuchao Pang, Bo Yan, Haihua Wang, Xianyun Qin
Publikováno v:
Gene. 554:101-104
Inguinal hernia is a common developmental disease in children and most cases are indirect inguinal hernia (IIH). Genetic factors have been suggested to play important roles in IIH. Although IIH has been observed in several human syndromes, genetic ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::293b8b4f5c3b97476d4791636a3daf0e
https://doi.org/10.1016/j.gene.2014.10.031
https://doi.org/10.1016/j.gene.2014.10.031
Publikováno v:
Gene. 547:86-90
Inguinal hernia is a common surgical disease, majority of which are indirect inguinal hernia (IIH). A positive family history has indicated that genetic factors play important roles in the IIH development. To date, genetic causes and underlying mecha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d57d8d97d9dbd7769b4ab62498ecb26d
https://doi.org/10.1016/j.gene.2014.06.030
https://doi.org/10.1016/j.gene.2014.06.030
Publikováno v:
Gene. 508:106-109
Congenital heart disease (CHD) is one of the most common birth defects in humans. Mutations in cardiac transcription factor genes, such as GATA4, NKX2-5 and TBX5 genes, have been associated to a small portion of familial and isolated CHD cases. NKX2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2425fca2401215a8eb8073ba40714e0
https://doi.org/10.1016/j.gene.2012.07.019
https://doi.org/10.1016/j.gene.2012.07.019
Publikováno v:
Gene. 500:28-31
Congenital heart disease (CHD) is the most common human birth defect. The morbidity and mortality of CHD patients are significantly higher than normal population even after surgical correction of cardiac defects, which is likely caused by genetic def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a02f4b20ea95b5b7ded4d860d6ae106
https://doi.org/10.1016/j.gene.2012.03.055
https://doi.org/10.1016/j.gene.2012.03.055
Publikováno v:
Gene. 546(1)
Inguinal hernia is a common surgical disease, for which genetic factors have been suggested to play a role. Sirtuin 1 (SIRT1), a highly conserved NAD-dependent class III deacetylase, has been implicated in human diseases. Since SIRT1 regulates differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::669d1999f8d81c621480fff0cff48adf
https://pubmed.ncbi.nlm.nih.gov/24875419
https://pubmed.ncbi.nlm.nih.gov/24875419
Publikováno v:
Gene. 535(2)
Inguinal hernia is a common disease, most cases of which are indirect inguinal hernia (IIH). Genetic factors play an important role for inguinal hernia. Increased incidences of inguinal hernia have been reported in patients with 22q11.2 microdeletion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f388c922dde57e23e8d85407aec0adab
https://pubmed.ncbi.nlm.nih.gov/24295890
https://pubmed.ncbi.nlm.nih.gov/24295890
Autor:
Guanghua Wu, Jiping Shan, Liming Ma, Shuchao Pang, Hongxin Wanyan, Yanli Qiao, Xianyun Qin, Bo Yan, Qining Xing
Publikováno v:
Pediatric cardiology. 33(8)
The ventricular septal defect (VSD) is the most common type of congenital heart disease (CHD). The morbidity and mortality of CHD patients are significantly higher due to late cardiac complications, likely caused by genetic defects. Mutations in card
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec1eba5f09fabb10f280ea933cff0406
https://pubmed.ncbi.nlm.nih.gov/22576768
https://pubmed.ncbi.nlm.nih.gov/22576768
Autor:
Haihua Wang, Jiping Shan, Guanghua Wu, Shuchao Pang, Bo Yan, Hongxin Wanyan, Yanli Qiao, Qining Xing, Liming Ma
Publikováno v:
Translational Research. 160:237-238
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e404600fc12a6a39a586a369991783c7
https://doi.org/10.1016/j.trsl.2012.04.003
https://doi.org/10.1016/j.trsl.2012.04.003
Autor:
Yuangang Qiao1, Zhiping Zhang2, Wenhui Huang3, Shuchao Pang3, Qining Xing4, Bo Yan3,5 yanbmd@gmail.com
Publikováno v:
Gene. Aug2014, Vol. 547 Issue 1, p86-90. 5p.