Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Riyaz Ahmad Pandit"'
Publikováno v:
Gene. 516:316-319
Prolidase deficiency (PD) is a rare inborn disorder of collagen metabolism characterized by chronic recurrent cutaneous ulceration. We report a novel 3 bp insertion in the 12th exon of the PEPD gene in two Kashmiri siblings with prolidase deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42ae6f432353e1029fe9b397c0ab3c0c
https://doi.org/10.1016/j.gene.2012.12.070
https://doi.org/10.1016/j.gene.2012.12.070
Autor:
Chanan Angsuthanasombat, Riyaz Ahmad Pandit, Gerd Katzenmeier, Wanpen Chaicumpa, Kanungsuk Meetum, Kittipong Suvarnapunya
Publikováno v:
Biochemical and biophysical research communications. 466(1)
The 126-kDa Bordetella pertussis CyaA-hemolysin (CyaA-Hly) was previously expressed in Escherichia coli as a soluble precursor that can be acylated to retain hemolytic activity. Here, we investigated structural and functional characteristics of a ∼
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3de37eb7ef76cb08e2f1697625f6f40
https://pubmed.ncbi.nlm.nih.gov/26325465
https://pubmed.ncbi.nlm.nih.gov/26325465
Autor:
Kanokporn Triwitayakorn, Suthat Fucharoen, Saovaros Svasti, Pranee Winichagoon, Chayanon Peerapittayamongkol, Riyaz Ahmad Pandit, Thongperm Munkongdee, Orapan Sripichai
Publikováno v:
International journal of hematology. 88(4)
Increase in fetal hemoglobin (Hb F) reduces globin chain imbalance in beta-thalassemia, consequently improving symptoms. QTL mapping together with previous genome-wide association study involving approximately 110,000 gene-based SNPs in mild and seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::695b3c0aeaa991708e0e56b2756a87d9
https://pubmed.ncbi.nlm.nih.gov/18839276
https://pubmed.ncbi.nlm.nih.gov/18839276