Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Waseem Chauhan"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Background The apolipoprotein A5 (APOA5) gene, significantly expressed in liver, has been involved in regulation of triglyceride metabolism, plasma lipid levels, serum adipokine levels and cardiovascular traits. A single-nucleotide polymorph
Externí odkaz:
https://doaj.org/article/c2e9c4678fbd49c88a7341c98d195cf0
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Due to indels in the β-globin gene, patients with β-thalassemia major exhibit a range of severity, with genotype β0β0 > β0β+ > β+β+, according to the production level of the β-globin chain. More than 300 mutations have be
Externí odkaz:
https://doaj.org/article/fb010e0b638c40d3bd0858d1db15143a
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-24 (2022)
Abstract Background Single nucleotide polymorphism (SNP) variants are abundant, persistent and widely distributed across the genome and are frequently linked to the development of genetic diseases. Identifying SNPs that underpin complex diseases can
Externí odkaz:
https://doaj.org/article/bfe3f497fccb4a82be2246159b48e737
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
BackgroundBrain-derived neurotrophic factor (BDNF), a neurotransmitter modulator, plays a significant role in neuronal survival and growth and participates in neuronal plasticity, thus being essential for learning, memory, and the development of cogn
Externí odkaz:
https://doaj.org/article/43adf0c52f664c10af2cb3938f0ee130
Publikováno v:
Diabetes Epidemiology and Management, Vol 7, Iss , Pp 100097- (2022)
Current global estimates suggest that more than 537 million young adults are living with diabetes worldwide, which has become a serious health burden. From the genetic perspective, diabetes falls into two categories, viz. monogenic and polygenic diab
Externí odkaz:
https://doaj.org/article/a9aa3da6d8384e578a53cfa159b676f6
Autor:
Waseem Chauhan, Rahima Zennadi
Publikováno v:
Antioxidants, Vol 12, Iss 3, p 740 (2023)
Sickle cell disease (SCD) is a monogenic inheritable disease characterized by severe anemia, increased hemolysis, and recurrent, painful vaso-occlusive crises due to the polymerization of hemoglobin S (HbS)-generated oxidative stress. Up until now, o
Externí odkaz:
https://doaj.org/article/df479b1cd2194e738ff8b4dc6fc17070
Autor:
Shoaib Shoaib, Mohammad Azam Ansari, Geetha Kandasamy, Rajalakshimi Vasudevan, Umme Hani, Waseem Chauhan, Maryam S. Alhumaidi, Khadijah A. Altammar, Sarfuddin Azmi, Wasim Ahmad, Shadma Wahab, Najmul Islam
Publikováno v:
Molecules, Vol 28, Iss 2, p 795 (2023)
The novel pathogenic virus was discovered in Wuhan, China (December 2019), and quickly spread throughout the world. Further analysis revealed that the pathogenic strain of virus was corona but it was distinct from other coronavirus strains, and thus
Externí odkaz:
https://doaj.org/article/e13998ebb2bb426a80f7ff4e6a8c0c56
Publikováno v:
Genes & Genomics. 45:813-825
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c475ebee203329405b20c14acc585bf3
https://doi.org/10.1007/s13258-023-01367-9
https://doi.org/10.1007/s13258-023-01367-9
Publikováno v:
British Journal of Clinical Pharmacology. 88:3610-3626
Beta-thalassaemia, including sickle cell anaemia and thalassaemia E, is most common in developing countries in tropical and subtropic regions. Because carriers have migrated there owing to demographic migration, β-thalassaemia can now be detected in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00696bf1c8f2a86e44f02e9c6c60ccb
https://doi.org/10.1111/bcp.15343
https://doi.org/10.1111/bcp.15343
Publikováno v:
Asian Pacific Journal of Health Sciences. 8:41-47
Introduction: Deficiency of glucose-6-phosphate dehydrogenase (G6PD) enzyme in erythrocytes is among the prevalent X-linked recessive genetic disorders and affects approximately 400 million people across the globe. It causes neonatal hyperbilirubinem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f4a4a66e3a6ef537d321c7192ef0fdb
https://doi.org/10.21276/apjhs.2021.8.4.06
https://doi.org/10.21276/apjhs.2021.8.4.06