Hexose monophosphate shunt, the role of its metabolites and associated disorders: A review

Author:

Akram Muhammad1,Ali Shah Syed Muhammad1,Munir Naveed23,Daniyal Muhammad4,Tahir Imtiaz Mahmood2,Mahmood Zahed3,Irshad Muhammad5,Akhlaq Muhammad6,Sultana Sabira1,Zainab Rida1ORCID

Affiliation:

1. Department of Eastern Medicine Directorate of Medical Sciences, Government College University Faisalabad Pakistan

2. College of Allied Health Professional, Directorate of Medical Sciences, Government College University Faisalabad Pakistan

3. Department of Biochemistry Government College University Faisalabad Pakistan

4. TCM and Ethnomedicine Innovation & Development International Laboratory, School of Pharmacy, Hunan University of Chinese Medicine Changsha China

5. Department of Chemistry University of Kotli, Azad Jammu & Kashmir (UoKAJK) Pakistan

6. Department of Pharmaceutics Faculty of Pharmacy, Gomal University DIK KP Pakistan

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Reference82 articles.

1. Prevalence of glucose‐6‐phosphate dehydrogenase deficiency among male donors in Shiraz, southern Iran;Amoozegar H.;Iranian Journal of Medical Sciences,2015

2. Novel Heterozygous Mutations in TALDO1 Gene Causing Transaldolase Deficiency and Early Infantile Liver Failure

3. Serum soluble transferrin receptor concentrations are elevated in congolese children with glucose‐6‐phosphate dehydrogenase variants, but not sickle cell variants or α‐thalassemia;Barker M. K.;The Journal of Nutrition,2017

4. Hereditary Hemolytic Anemia Associated with Glucosephosphate Isomerase (GPI) Deficiency— a New Enzyme Defect of Human Erythrocytes

5. Maternal consumption of quinine-containing sodas may induce G6PD crises in breastfed children

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