Zobrazeno 1 - 10
of 164
pro vyhledávání: '"B H, Paw"'
Autor:
Waheed, Marwa1 (AUTHOR), Hussain, Muhammad Bilal1 (AUTHOR), Saeed, Farhan1 (AUTHOR), Afzaal, Muhammad1 (AUTHOR) muhammadafzaal@gcuf.edu.pk, Ahmed, Aftab2 (AUTHOR), Irfan, Rushba3 (AUTHOR), Akram, Noor4 (AUTHOR), Ahmed, Faiyaz5 (AUTHOR), Hailu, Gebremichael Gebremedhin6 (AUTHOR) mikialejr@gmail.com
Publikováno v:
Food Science & Nutrition. Dec2024, Vol. 12 Issue 12, p9893-9912. 20p.
Autor:
A C, Oates, A, Brownlie, S J, Pratt, D V, Irvine, E C, Liao, B H, Paw, K J, Dorian, S L, Johnson, J H, Postlethwait, L I, Zon, A F, Wilks
Publikováno v:
Blood. 94(8)
Members of the JAK family of protein tyrosine kinase (PTK) proteins are required for the transmission of signals from a variety of cell surface receptors, particularly those of the cytokine receptor family. JAK function has been implicated in hematop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d22529b80282a7eacddbae28ba59055
https://pubmed.ncbi.nlm.nih.gov/10515866
https://pubmed.ncbi.nlm.nih.gov/10515866
Autor:
A C, Oates, P, Wollberg, S J, Pratt, B H, Paw, S L, Johnson, R K, Ho, J H, Postlethwait, L I, Zon, A F, Wilks
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 215(4)
Transcription factors of the STAT family are required for cellular responses to multiple signaling molecules. After ligand binding-induced activation of cognate receptors, STAT proteins are phosphorylated, hetero- or homodimerize, and translocate to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f84ed23ca7e0dcae812a402ac47ce75
https://pubmed.ncbi.nlm.nih.gov/10417824
https://pubmed.ncbi.nlm.nih.gov/10417824
Publikováno v:
Methods in cell biology. 59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::36cf2141170e34e3a10e52b9b59578ee
https://pubmed.ncbi.nlm.nih.gov/9891354
https://pubmed.ncbi.nlm.nih.gov/9891354
Publikováno v:
American journal of human genetics. 47(4)
Mutations in the HEX A gene, encoding the alpha-subunit of beta-hexosaminidase A (Hex A), are the cause of Tay-Sachs disease as well as of juvenile, chronic, and adult GM2 gangliosidoses. We have examined the distribution of three mutations--a 4-nucl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c1277e653633c7505b02ed0ce1ca77c
https://pubmed.ncbi.nlm.nih.gov/2220809
https://pubmed.ncbi.nlm.nih.gov/2220809
Publikováno v:
The Journal of biological chemistry. 265(16)
Juvenile GM2 gangliosidosis is a rare neurodegenerative disorder closely related to Tay-Sachs disease but of later onset and more protracted course. The biochemical defect lies in the alpha-subunit of the lysosomal enzyme beta-hexosaminidase. Culture
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7dc9216429a794f0d06f31bdd175c7b1
https://pubmed.ncbi.nlm.nih.gov/2140574
https://pubmed.ncbi.nlm.nih.gov/2140574
Autor:
Yulu Yang, Xianhui Zhang, Yao Yang, Pengfei Gao, Wuzhe Fan, Tao Zheng, Weihu Yang, Yu Tang, Kaiyong Cai
Publikováno v:
Bioactive Materials; Nov2024, Vol. 41, p336-354, 19p
Autor:
Song, Jia1,2,3 (AUTHOR), Zhang, Yuning4 (AUTHOR), Bai, Yunyang1,3 (AUTHOR), Sun, Xiaowen2 (AUTHOR), Lu, Yanhui2 (AUTHOR), Guo, Yusi1,3 (AUTHOR), He, Ying1,3 (AUTHOR), Gao, Min1,3 (AUTHOR), Chi, Xiaopei1,3 (AUTHOR), Heng, Boon Chin3,5 (AUTHOR), Zhang, Xin6 (AUTHOR), Li, Wenjing1,3 (AUTHOR), Xu, Mingming1,3 (AUTHOR), Wei, Yan1,3 (AUTHOR), You, Fuping6 (AUTHOR) fupingyou@bjmu.edu.cn, Zhang, Xuehui2,3,7 (AUTHOR) zhangxuehui@bjmu.edu.cn, Lu, Dan6 (AUTHOR) taotao@bjmu.edu.cn, Deng, Xuliang1,3,7 (AUTHOR) kqdengxuliang@bjmu.edu.cn
Publikováno v:
Advanced Science. 10/26/2023, Vol. 10 Issue 30, p1-16. 16p.
Autor:
Zeng, Fantian1 (AUTHOR), Nijiati, Sureya1 (AUTHOR), Tang, Longguang2 (AUTHOR), Ye, Jinmin1 (AUTHOR), Zhou, Zijian1,3 (AUTHOR) zhouz@xmu.edu.cn, Chen, Xiaoyuan4,5,6,7 (AUTHOR) chen.shawn@nus.edu.sg
Publikováno v:
Angewandte Chemie. 8/28/2023, Vol. 135 Issue 35, p1-26. 26p.
Normal transcription of the beta-hexosaminidase alpha-chain gene in the Ashkenazi Tay-Sachs mutation
Autor:
B H, Paw, E F, Neufeld
Publikováno v:
The Journal of biological chemistry. 263(6)
Tay-Sachs disease is a biochemically heterogeneous lysosomal storage disorder caused by lack of the A isoenzyme of beta-hexosaminidase; the underlying defect is a mutation in the gene encoding the alpha-chain. It has been shown that fibroblasts isola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a123ef7a5ef2d6bbb468c9514938183e
https://pubmed.ncbi.nlm.nih.gov/2449434
https://pubmed.ncbi.nlm.nih.gov/2449434