Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pingming Gao"'
Autor:
Li Xiao, Min Wang, Wanhua Zhang, Yuan Song, Jiaying Zeng, Huilin Li, Hong Yu, Ling Li, Pingming Gao, Paul Yao
Publikováno v:
BMC Neuroscience, Vol 23, Iss 1, Pp 1-14 (2022)
Abstract Background Retinoic acid-related orphan receptor alpha (RORA) has been reported to be suppressed in autistic patients and is associated with autism spectrum disorders (ASD), although the potential role and mechanism of RORA on gastrointestin
Externí odkaz:
https://doaj.org/article/9aae774e1b1a4d56bd942741906f1937
Autor:
Jiaojiao Ren, Zhenghe Wang, Yujie Zhang, Peidong Zhang, Jianmeng Zhou, Wenfang Zhong, Xing Wang, Pingming Gao, Xiaoming Shi, Chen Mao
Publikováno v:
Frontiers in Public Health, Vol 9 (2021)
Introduction: The association patterns of hemoglobin (HB) concentrations with mortality among the longevity older adults are unclear. We aimed to evaluate the relationship among older adults form Chinese longevity regions.Methods: We included 1,785 o
Externí odkaz:
https://doaj.org/article/f3467e4b3b3f495c83787a04b7aaf597
Autor:
Jiaojiao Ren, Peidong Zhang, Zhihao Li, Xiru Zhang, Dong Shen, Peiliang Chen, Qingmei Huang, Pingming Gao, Chen Mao
Publikováno v:
International Journal of Cancer. 152:1778-1788
Whether screening can attenuate the influence of genetic risk and environmental risk factors for colorectal cancer (CRC) mortality risk remains unknown. Our study is to investigate the association of the screening history, genetic risk and environmen
Autor:
Xiaoying, He, Zhuobin, Jiang, Basma, Nasr, Cuiling, Wu, Saijun, Huang, Pingming, Gao, Yanna, Zhu
Publikováno v:
Annals of Nutrition and Metabolism. 78:187-196
Introduction: Premature infants are exceptionally vulnerable to nutrition-related diseases, and the utilization of standardized feeding guidelines may reduce nutritional practice variation, which can promote growth. Nutritional risk screening is the
Autor:
Jiaojiao Ren, Peidong Zhang, Zhihao Li, Xiru Zhang, Wenfang Zhong, Weiqi Song, Xing Wang, Pingming Gao, Chen Mao
Publikováno v:
Cancers; Volume 14; Issue 20; Pages: 5138
Regular use of non-steroidal anti-inflammatory drugs (NSAIDs) was associated with the lower risk of colorectal cancer (CRC). However, whether regular use of NSAIDs could attenuate the effect of genetic risk and environmental risk factors on CRC is un
Autor:
Mi Luo, Zhuohong Tang, Qingmei Lin, Peng Huang, Xing Wang, Shuwen Liu, Zihao He, Pingming Gao, Ting Luo, Jianghua Zhu
Publikováno v:
Food & Function. 12:11174-11189
Gestational diabetes mellitus (GDM) has become a global health concern as the main result of its contribution to the high risk of adverse pregnancy outcomes for both the mother and fetus. However, there is absence of an ideal and widely acceptable th
Autor:
Li Xiao, Min Wang, Wanhua Zhang, Yuan Song, Jiaying Zeng, Huilin Li, Hong Yu, Ling Li, Pingming Gao, Paul Yao
Publikováno v:
BMC neuroscience. 23(1)
Background Retinoic acid-related orphan receptor alpha (RORA) has been reported to be suppressed in autistic patients and is associated with autism spectrum disorders (ASD), although the potential role and mechanism of RORA on gastrointestinal (GI) s
Autor:
Xiaotong Wang, Jiajia Jing, Saijun Huang, Xiaoying He, Pingming Gao, Hailin Li, Zongyu Lin, Per Torp Sangild, Yanna Zhu
Publikováno v:
Nutrients; Volume 14; Issue 22; Pages: 4931
Anemia is associated with neurodevelopmental delays and brain injury in infants and toddlers, but whether early anemia has a similar effect in neonatal preterm infants is largely unknown. Thus, this study aimed to determine the relationship of early
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 43(2)
Rolandic epilepsy (RE) is among the most common focal epilepsies in childhood. For the majority of patients with RE and atypical RE (ARE), the etiology remains elusive. We thus screened patients with RE/ARE in order to detect disease-causing variants
Publikováno v:
Renal failure. 36(9)
NPHS2 mutations are responsible for autosomal recessive familial steroid-resistant nephrotic syndrome (SRNS) with minor glomerular abnormalities or focal segmental glomerulosclerosis (FSGS), which is characterized by early childhood onset and rapid p