Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Endom Ismail"'
Autor:
Mohamed Afiq Hidayat Zailani, Raja Zahratul Azma Raja Sabudin, Azlin Ithnin, Hafiza Alauddin, Siti Aishah Sulaiman, Endom Ismail, Ainoon Othman
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder and a global public health concern that is most prevalent in malaria-endemic regions including Asia, Africa, and the Mediterranean. G6PD-deficient indi
Externí odkaz:
https://doaj.org/article/ede23874844e4c2a97711305a5be3024
Autor:
Danny Xuan-Rong Koh, Mohamed Afiq Hidayat Zailani, Raja Zahratul Azma Raja Sabudin, Sanggari Muniandy, Nur Awatif Akmal Muhamad Hata, Siti Noor Baya Mohd Noor, Norhazilah Zakaria, Ainoon Othman, Endom Ismail
Publikováno v:
PLoS ONE, Vol 18, Iss 12 (2023)
Externí odkaz:
https://doaj.org/article/34bafe750bd94dfeae87b2955db491a0
Autor:
Endom Ismail, Omimah Khaled Jaber Nofal, Rajalingham Sakthiswary, Syahrul Sazliyana Shaharir, Radhika Sridharan
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0153752 (2016)
Interleukin-1 receptor antagonist (IL-1Ra) acts as an inhibitor of IL-1; which is one of the culprit cytokines in rheumatoid arthritis (RA). Although +2018 polymorphism of IL-1Ra has been implicated in the pathogenesis of RA, its importance remains p
Externí odkaz:
https://doaj.org/article/d4fda3fe599647e9b5eb756e0d563593
Autor:
Khairina Kamarudin, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Loh C-Khai, Norunaluwar Jalil, Danny Koh-Xuan-Rong, Azlin Ithnin, Tang Yee Loong, Endom Ismail, Ainoon Othman, Hamidah Alias, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 42:247-251
Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice site mutation interferes with normal splicing of pre mRNA and results in activation of a cryp
Autor:
Ainoon Othman, Danny Xuan Rong Koh, Endom Ismail, Rahimah Ahmad, Raja Zahratul Azma Raja Sabudin, Malisa Mohd Yusoff, Noor Hamidah Hussin
Publikováno v:
Annals of Human Genetics. 81:205-212
Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the prevalence and common mutations among the indigenous people. This cross-sectional study was perform
Publikováno v:
Medicine & Health. 11:209-217
The search for novel biomarkers has taken centre stage in the past decades of research in Rheumatoid Arthritis (RA). The purpose of the present study was to determine the correlation of serum matrix metalloproteinase-3 (MMP-3) with disease activity,
Autor:
Farahnaz Amini, Endom Ismail
Publikováno v:
Journal of Human Genetics. 58:189-194
The combination of two silent mutations, c.1311CT in exon 11 and IVS11 T93C (glucose-6-phosphate dehydrogenase (G6PD) 1311T/93C), with unknown mechanism, have been reported in G6PD-deficient individuals in Asian populations including Malaysian aborig
Publikováno v:
Asian Journal of Animal and Veterinary Advances. 8:63-72
The genetic structure of horseshoe crab (Tachypleus gigas) populations were examined using 18 microsatellite markers. Samples were collected from 2 stations of east coast of Peninsular Malaysia and one station from East Malaysia. All the observed all
Autor:
Danny Xuan Rong, Koh, Raja Zahratul Azma, Raja Sabudin, Malisa, Mohd Yusoff, Noor Hamidah, Hussin, Rahimah, Ahmad, Ainoon, Othman, Endom, Ismail
Publikováno v:
Annals of human genetics. 81(5)
Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the prevalence and common mutations among the indigenous people. This cross-sectional study was perform
Autor:
Omimah Khaled Jaber Nofal, Syahrul Sazliyana Shaharir, Endom Ismail, Rajalingham Sakthiswary, Radhika Sridharan
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0153752 (2016)
PLoS ONE
PLoS ONE
Objective Interleukin-1 receptor antagonist (IL-1Ra) acts as an inhibitor of IL-1; which is one of the culprit cytokines in rheumatoid arthritis (RA). Although +2018 polymorphism of IL-1Ra has been implicated in the pathogenesis of RA, its importance