Neonatal Sickle Cell Disease Assessment in Rural Indian Community: Demand for Point of Care Testing (POCT)
Neonatal Sickle Cell Disease Assessment in Rural Indian Community: Demand for Point of Care Testing (POCT)

Sarita Anil Shinde; Anita Deepak Deshmukh; Umesh Kisanrao More

Volume 7, Issue 1 , January 2024, , Pages 1-8

https://doi.org/10.26655/JMCHEMSCI.2024.1.1

Abstract
  The most prevalent hemoglobinopathy is sickle cell disease, which is followed by β-thalassemia and thalassemia syndrome. The Mediterranean region, Middle East, Indian subcontinent, ...  Read More
Haemoglobin Variant Study by HPLC Method at a Tertiary Care Centre
Haemoglobin Variant Study by HPLC Method at a Tertiary Care Centre

Pradnya Phalak; Abhijit Pratap

Volume 6, Issue 11 , November 2023, , Pages 2841-2848

https://doi.org/10.26655/JMCHEMSCI.2023.11.29

Abstract
  Haemoglobinopathies are genetic disorders arising due to defect in the globin chain of haemoglobin. It is relatively common amongst genetic disorders. Beta thalassemia and Sickle cell ...  Read More
Association of BCL11A Gene Polymorphism in Human Cells of Thalassemia Patient by Evaluation of Amplification Refractory Mutation System (ARMS)
Association of BCL11A Gene Polymorphism in Human Cells of Thalassemia Patient by Evaluation of Amplification Refractory Mutation System (ARMS)

Zahraa Qasim Mousa; Maytham A. Dragh

Volume 6, Issue 4 , April 2023, , Pages 834-845

https://doi.org/10.26655/JMCHEMSCI.2023.4.15

Abstract
  Thalassemia is an autosomal recessive disorder. It occurs due to mutations that lead to a decrease or absence of β-globin chains. In human erythroid cells, it was found that BCL11A ...  Read More
The Study of BCL11A Gene in Patients with Beta-Thalassemia Major and Intermedia by Random Amplephed Polymorphism DNA in Iraq
The Study of BCL11A Gene in Patients with Beta-Thalassemia Major and Intermedia by Random Amplephed Polymorphism DNA in Iraq

Zahraa Qasim Mousa; Maytham A. Dragh

Volume 6, Issue 4 , April 2023, , Pages 846-856

https://doi.org/10.26655/JMCHEMSCI.2023.4.16

Abstract
  Thalassemia Autosomal recessive disorders occur due to mutations that lead to a decrease or absence of b-globin chains because mutations occur in the BCL11A gene being a potential therapeutic ...  Read More