Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jyotdeep Kour Raina"'
Autor:
Jyotdeep Kour Raina, Rakesh Kumar Panjaliya, Vikas Dogra, Sushil Sharma, Anupriya, Parvinder Kumar
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-21 (2022)
Abstract Background The risk of Congenital Heart Defects (CHD) is greatly influenced by variants within the genes involved in folate-homocysteine metabolism. Polymorphism in MTHFR (C677T and G1793A) and MS/MTR (A2756G) genes increases the risk of dev
Externí odkaz:
https://doaj.org/article/db9320a7f18e4d0ab6a624b5c7c25478
Autor:
Jyotdeep Kour Raina, Minakashee Sharma, Rakesh Kumar Panjaliya, Vikas Dogra, Ashok Bakaya, Parvinder Kumar
Publikováno v:
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-13 (2020)
Abstract Background Coronary artery disease (CAD) is a complex disease resulting from the cumulative and interactive effects of large number of genes along with environmental exposure. Therefore, the present study was envisaged as an effort to study
Externí odkaz:
https://doaj.org/article/5868707a52434e58a313e7e2f52e4c85
Autor:
Sawan Kumar, Jyotdeep Kour Raina, Amrit Sudershan, Kanak Mahajan, Raman Jasrotia, Chinmoyee Maharana, Rakesh K. Panjalia, Parvinder Kumar
Publikováno v:
European Neurology. 86:55-62
Introduction: Migraine is a neurovascular disorder and is clinically characterized by episodic attacks of mild to severe headaches. Due to the involvement of multiple environmental and genetic factors, it has become a much more complex neurological c
Autor:
Ankush Bala, Jyotdeep Kour Raina, Amrit Sudershan, Sanjeev Digra, Manoj K. Dhar, Rakesh K. Panjaliya, Parvinder Kumar
Publikováno v:
Indian Journal of Medical Sciences. 74:126-133
Objectives: There are many multifactorial causes for Congenital Heart Defects (CHDs) in which both genetic and non-genetic factors play role. MTHFD1 and CBS are two of the key enzymes that plays pivotal role in the metabolic pathway of homocysteine.
Autor:
Jyotdeep Kour Raina
Publikováno v:
Bioscience Biotechnology Research Communications. 13:610-615