Makia F. Nasir
Multan, PB, Pakistan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Corrigendum: Disease specific symptoms indices in patients with celiac disease-A hardly recognised entity.
Journal: Frontiers in nutrition
Published: October 18, 2022
Genetic variation between hybrid (Labeo rohita ♂, Cirrhinus mrigala ♀ and Labeo rohita) by RAPD marker.
Journal: Brazilian journal of biology = Revista brasleira de biologia
Published: October 10, 2022
Molecular based identification and phylogenetic relationship by using cytochrome b gene of Pangasius pangasius.
Journal: Brazilian journal of biology = Revista brasleira de biologia
Published: September 19, 2022
Disease specific symptoms indices in patients with celiac disease-A hardly recognised entity.
Journal: Frontiers in nutrition
Published: May 15, 2022
Assessment of renal and hepato-protective potential of guava leaves in male Sprague dawley rats.
Journal: Cellular and molecular biology (Noisy-le-Grand, France)
Published: March 07, 2021
Hyperhomocysteinemia as an Independent Risk Factor for Coronary Heart Disease. Comparison with Conventional Risk Factors.
Journal: Brazilian journal of biology = Revista brasleira de biologia
Published: February 24, 2021
Amelioration potential of Moringa oleifera extracts against sodium arsenate induced embryotoxicity and genotoxicity in mouse (Mus musculus).
Journal: Brazilian journal of biology = Revista brasleira de biologia
Published: January 27, 2021
Tudor tells about new twists in the story tale of SMURFs.
Journal: Cellular and molecular biology (Noisy-le-Grand, France)
Published: April 22, 2016
Alpha-lipoic acid: An inimitable feed supplement for poultry nutrition.
Journal: Journal of animal physiology and animal nutrition
Published: December 12, 2015
Genetic association analysis of serotonin transporter polymorphism (5-HTTLPR) with type 2 diabetes patients of Pakistani population.
Journal: Diabetes research and clinical practice
Published: September 19, 2014
Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family.
Journal: Clinical genetics
Published: July 16, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026