Nida Ajmal
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7936 Type 1 Diabetes Therapeutic Compound MSB-61: Using RNA Sequencing To Identify The Mechanism Open
Disclosure: P. Khan: None. K. Corbin: None. N. Ajmal: None. S. Bergmeir: None. G. Gu: None. X. Tong: None. C.S. Nunemaker: None. Abstract Type 1 diabetes (T1D) is a chronic autoimmune disease in which loss of insulin-producing beta-cells l…
8010 Potent MSB-61 as Type 1 Diabetes (T1D) therapy: mechanism of action in insulin secretion Open
Disclosure: N. Ajmal: None. M. Bogart: None. K. Corbin: None. P. Khan: None. M. Shafqat: None. S. Bergmeier: None. G. Gu: None. X. Tong: None. C.S. Nunemaker: None. Type 1 diabetes (T1D) is a chronic autoimmune disorder caused by proinflam…
Identifying Promising Immunomodulators for Type 1 Diabetes (T1D) and Islet Transplantation Open
Type 1 diabetes (T1D) is an autoimmune chronic disorder that damages beta cells in the pancreatic islets of Langerhans and results in hyperglycemia due to the loss of insulin. Exogenous insulin therapy can save lives but does not stop dise…
Emerging Anti-Diabetic Drugs for Beta-Cell Protection in Type 1 Diabetes Open
Type 1 diabetes (T1D) is a chronic autoimmune disorder that damages beta cells in the pancreatic islets of Langerhans and results in hyperglycemia due to the loss of insulin. Exogenous insulin therapy can save lives but does not halt disea…
DMD Gene Mutation identification in Duchenne Muscular Dystrophy Patients of Quetta, Balochistan, Pakistan Open
Duchenne Muscular Dystrophy (DMD) is the most common inherited muscular disorder in children. It is caused by mutations in DMD gene which encodes dystrophin protein. Mutation analysis has been challenging in DMD gene due to its large size …
Polycystic ovary syndrome (PCOS) and genetic predisposition: A review article Open
Polycystic ovary syndrome (PCOS) is a heterogeneous condition which is related to an endocrine reproductive disorder of females. It affects females of 18-44 age. The persistent hormonal disbalance leads to the complexities such as numerous…