Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Omran, Rashidi"'
Autor:
Arwa Mastoor Alharthi, Babajan Banaganapalli, Sabah M. Hassan, Omran Rashidi, Bandar Ali Al-Shehri, Meshari A. Alaifan, Bakr H. Alhussaini, Hadeel A. Alsufyani, Kawthar Saad Alghamdi, Khalda Khalid Nasser, Yagoub Bin-Taleb, Ramu Elango, Noor Ahmad Shaik, Omar I. Saadah
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundAutoimmune diseases (AIDs) share a common molecular etiology and often present overlapping clinical presentations. Thus, this study aims to explore the complex molecular basis of AID by whole exome sequencing and computational biology analy
Externí odkaz:
https://doaj.org/article/c46bf0689f4942c6940e515e4bc91d32
Autor:
Jumana Yousuf Al-Aama, Noor Ahmad Shaik, Babajan Banaganapalli, Mohammed A Salama, Omran Rashidi, Ahmed N Sahly, Mohammed O Mohsen, Harbi A Shawoosh, Hebah Ahmad Shalabi, Mohammad Al Edreesi, Sameer E Alharthi, Jun Wang, Ramu Elango, Omar I Saadah
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176664 (2017)
Celiac disease (CD), a multi-factorial auto-inflammatory disease of the small intestine, is known to occur in both sporadic and familial forms. Together HLA and Non-HLA genes can explain up to 50% of CD's heritability. In order to discover the missin
Externí odkaz:
https://doaj.org/article/131ed546c31e47ea901ac980cfc0d987
Autor:
Babajan, Banaganapalli, Omran, Rashidi, Omar I, Saadah, Jun, Wang, Imran Ali, Khan, Jumana Y, Al-Aama, Noor Ahmad, Shaik, Ramu, Elango
Publikováno v:
Journal of cellular biochemistry. 118(8)
Celiac disease (CD) is a gluten intolerance disorder with known genetic contribution. The recent fine mapping and genome-wide association studies (GWAS) have identified up to 57 non-HLA CD susceptibility SNPs, majority of which are non-coding variant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee2be7bd4034f98636676d67221b808b
https://pubmed.ncbi.nlm.nih.gov/28059456
https://pubmed.ncbi.nlm.nih.gov/28059456