Physicochemical Properties and Potential Biological Activity of Conjugated Linoleic Acid Microcapsules from Tan Sheep Tail Fat

Authors: PEI Huimin, LI Yalei, CAO Songmin, LUO Ruiming, BI Yongzhao, FU Qihua

Source: Shipin Kexue, Vol 45, Iss 4, Pp 68-76 (2024)

Subject Terms: conjugated linoleic acid microcapsules, physicochemical properties, antioxidant activity, cholesterol lowering activity, Food processing and manufacture, TP368-456

File Description: electronic resource

Relation: https://www.spkx.net.cn/fileup/1002-6630/PDF/2024-45-4-009.pdf; https://doaj.org/toc/1002-6630

Access URL: https://doaj.org/article/017b4246e0514d5a8850d57f5766e78f

Effect of Adenosine 5’-Diphosphate Ribosylation on Meat Quality of Qinchuan Cattle

Authors: FU Qihua, LI Yalei, LUO Ruiming, WANG Xuerong, MA Xuhua

Source: Shipin Kexue, Vol 45, Iss 1, Pp 8-14 (2024)

Subject Terms: qinchuan cattle, longissimus dorsi muscle, adenosine 5’-diphosphate ribonylation, apoptosis, Food processing and manufacture, TP368-456

File Description: electronic resource

Relation: https://www.spkx.net.cn/fileup/1002-6630/PDF/2024-45-1-002.pdf; https://doaj.org/toc/1002-6630

Access URL: https://doaj.org/article/a4ecc14aebf04ab7afbe2974195c0837

Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities

Authors: Li, Niu ^{a, b, c, d, n}, Xu, Yufei ^{c, n}, Chen, Hongzhu ^{c, n}, Lin, Jingqi ^b, AlAbdi, Lama ^e, Bekheirnia, Mir Reza ^{f, g, h}, Li, Guoqiang ^{a, b}, Gofin, Yoel ^{f, g}, Bekheirnia, Nasim ^{g, h}, Faqeih, Eissa ⁱ, Chen, Lina ^c, Chang, Guoying ^j, Tang, Jie ^c, Yao, Ruen ^{c, d}, Yu, Tingting ^{c, d}, Wang, Xiumin ^j, Fu, Wei ^k, Fu, Qihua ^{k, l}, Shen, Yiping ^c, Alkuraya, Fowzan S. ^m, Machol, Keren ^{f, g, ∗}, Wang, Jian ^{b, c, d, l, ∗∗}

Source: In eBioMedicine January 2024 99

Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing

Authors: Ye, JiaJun, Niu, Yiwei, Peng, Yongxuan, Huang, Jihong, Wang, Huiying, Fu, Qihua, Li, Fen, Xu, Rang, Chen, Sun, Xu, Yuejuan, Sun, Kun

Source: In Genomics September 2023 115(5)

NEIL3 contributes to the Fanconi anemia/BRCA pathway by promoting the downstream double-strand break repair step

Authors: Li, Niu, Xu, Yufei, Chen, Hongzhu, Chen, Lina, Zhang, Yi, Yu, Tingting, Yao, Ruen, Chen, Jing, Fu, Qihua, Zhou, Jia, Wang, Jian

Source: In Cell Reports 8 November 2022 41(6)

Clinical features, laboratory findings and persistence of virus in 10 children with coronavirus disease 2019 (COVID-19)

Authors: Jiang, Hong, Cheng, Hongbin, Cao, Qing, Fei, Anxing, Yuan, Ming, Zhang, Lixia, Fei, Shinuan, Li, Jun, Yang, Shixiong, Wu, Jiang, Fu, Qihua, Li, Sheng, Zhang, Xiaoqing

Source: In Biomedical Journal February 2021 44(1):94-100

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing

Authors: Zu, Bailing, Zhang, Xiaoqing, Xu, Yunlan, Xiang, Ying, Wang, Zhigang, Cai, Haiqing, Wang, Bo, You, Guoling, Fu, Qihua

Source: In Computational and Structural Biotechnology Journal 2021 19:3482-3490

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families

Authors: Zu, Bailing, Wang, Zhigang, Xu, Yunlan, You, Guoling, Fu, Qihua

Source: Developmental dynamics. 250(9):1220-1228

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100129104142.0x000001&indx=1&recIds=ETOCvdc_100129104142.0x000001

Functional analysis of a novel pathogenic variant in CREBBP associated with bone development.

Authors: Fang, Qing, Xu, Yunlan, Feng, Jue, Zhang, Xiaoqing, Wang, Bo, Fu, Qihua, Xiang, Ying

Source: Pediatric Research; Dec2024, Vol. 96 Issue 7, p1626-1635, 10p

Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing

Authors: Shi, Xin, Zhang, Li, Bai, Kai, Xie, Huilin, Shi, Tieliu, Zhang, Ruilin, Fu, Qihua, Chen, Sun, Lu, Yanan, Yu, Yu, Sun, Kun

Source: In Computational and Structural Biotechnology Journal 2020 18:381-392

Intracellular osteopontin negatively regulates toll-like receptor 4-mediated inflammatory response via regulating GSK3β and 4EBP1 phosphorylation

Authors: Yang, Haiou, Ye, Xingchen, Zhang, Xiaoqing, Li, Xiaoliang, Fu, Qihua, Tang, Zhenhua

Source: In Cytokine August 2018 108:89-95

A novel dNTP-limited PCR and HRM assay to detect Williams-Beuren syndrome

Authors: Zhang, Lichen, Zhang, Xiaoqing, You, Guoling, Yu, Yongguo, Fu, Qihua

Source: In Clinica Chimica Acta June 2018 481:171-176

Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA–IVS in an Unselected Chinese Cohort

Authors: He, Xiaomin, Zhang, Xiaoqing, Jing, Hui, Zhang, Xiaoyang, Gao, Manchen, Chen, Huiwen, Geng, Juan, Zheng, Zhaojing, Fu, Qihua, Zhu, Zhongqun, Zheng, Jinghao

Source: Pediatric cardiology. 40(4):762-767

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100125570408.0x000001&indx=1&recIds=ETOCvdc_100125570408.0x000001

In vitro residual activities in 20 variants of phenylalanine hydroxylase and genotype-phenotype correlation in phenylketonuria patients

Authors: Zhang, Xia, Ye, Jun, Shen, Nan, Tao, Yue, Han, Lianshu, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Fan, Yanjie, Wang, Jianguo, Gong, Zhuwen, Wang, Yu, You, Guoling, Fu, Qihua, Mo, Xi, Gu, Xuefan, Yu, Yongguo

Source: Gene. 707:239-245

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100082052158.0x000001&indx=1&recIds=ETOCvdc_100082052158.0x000001

Identification of a novel ANO5 missense mutation in a Chinese family with familial florid osseous dysplasia

Authors: Lv, Mingming, You, Guoling, Wang, Jinbing, Fu, Qihua, Gupta, Anand, Li, Jun, Sun, Jian

Source: Journal of human genetics. 64(7):599-607

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100181235118.0x000001&indx=1&recIds=ETOCvdc_100181235118.0x000001

The clinical application and laboratory management of molecular genetic diagnosis in children's hospital.

Authors: Bao, Wenjie^1,2 (AUTHOR), Fu, Qihua³ (AUTHOR), Zhang, Xiaoqing³ (AUTHOR), Mo, Xi³ (AUTHOR), Yu, Tingting² (AUTHOR) ytt.007@163.com

Source: Clinical & Translational Discovery. Jun2024, Vol. 4 Issue 3, p1-13. 13p.

Subject Terms: *LABORATORY management, *CHILDREN'S hospitals, *GENETIC disorder diagnosis, *MOLECULAR diagnosis, *CLINICAL medicine

Association between CYP2C9 and VKORC1 genetic polymorphisms and efficacy and safety of warfarin in Chinese patients.

Authors: Zhang, Suli, Zhao, Mingzhe, Zhong, Shilong, Niu, Jiamin, Zhou, Lijuan, Zhu, Bin, Su, Haili, Cao, Wei, Xing, Qinghe, Yan, Hongli, Han, Xia, Fu, Qihua, Li, Qiang, Chen, Luan, Yang, Fan, Zhang, Na, Wu, Hao, He, Lin, Qin, Shengying

Source: Pharmacogenetics & Genomics; Jun2024, Vol. 34 Issue 4, p105-116, 12p

Corrigendum to 'Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene' [Stem Cell Res. 56 (2021) 102517]

Authors: Zu, Bailing, Zhang, Xiaoqing, You, Guoling, Fu, Qihua

Source: Stem cell research. 62

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100188122096.0x000001&indx=1&recIds=ETOCvdc_100188122096.0x000001

Novel TSC1 and TSC2 gene mutations in Chinese patients with tuberous sclerosis complex

Authors: Yu, Tingting, He, Yingzhong, Li, Niu, Zhou, Yunqing, Wang, Zhiping, Fu, Qihua, Wang, Jiwen, Wang, Jian

Source: In Clinical Neurology and Neurosurgery March 2017 154:104-108

Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects

Authors: Zhang, Erge, Hong, Nanchao, Chen, Sun, Fu, Qihua, Li, Fen, Yu, Yu, Sun, Kun

Source: Gene. 641:341-348

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100067077909.0x000001&indx=1&recIds=ETOCvdc_100067077909.0x000001