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pro vyhledávání: '"Fehmida Farid Khan"'
Autor:
null Sana, Sahfiq Ur Rahman, Muhammad Zahid, Ayaz Ali Khan, Tariq Aziz, Zafar Iqbal, Waqar Ali, Fehmida Farid Khan, Sumbal Jamil, Muhammad Shahzad, Metab Alharbi, Abdulrahman Alshammari
Publikováno v:
Acta biochimica Polonica.
Walnut Oil and Caralluma are edible and form part of the traditional medicine system in many countries. These are frequently used in traditional medicine as remedies to relieve a wide range of illnesses and health problems. Walnut Oil and Caralluma s
Autor:
Muhammad Naeem, Sakina Rehman, Muhammad Erfan, Uzma Ali, Fehmida Farid Khan, Naima Khan, Amir Ejaz, Zubair M. Ahmed
Publikováno v:
Biomolecules
Biomolecules, Vol 11, Iss 620, p 620 (2021)
Volume 11
Issue 5
Biomolecules, Vol 11, Iss 620, p 620 (2021)
Volume 11
Issue 5
Epidermolysis bullosa (EB) includes a group of rare gesnodermatoses that result in blistering and erosions of the skin and mucous membranes. Genetically, pathogenic variants in around 20 genes are known to alter the structural and functional integrit
Publikováno v:
Molecular biology reports. 46(1)
Pseudoxanthoma elasticum (PXE) is an autosomal recessive disorder of ectopic mineralization and fragmentation of elastic fibers in skin, eyes, cardiovascular and digestive system. PXE is caused by sequence variants in ABCC6, which encodes multidrug r
Autor:
Fehmida Farid Khan, Sobia Tabassum
Publikováno v:
Journal of Asian Scientific Research. 3(2):204-213
Congestive heart failure is a condition in which heart loses its ability to fill with or pump sufficient amount of blood through the body. Two cardiac natriuretic peptides aterial natriuretic peptide and brain natriuretic peptide are secreted by the
Publikováno v:
IOSR Journal of Pharmacy and Biological Sciences. 7:73-82
Parkinson's disease involves a progressive loss of midbrain dopaminergic neurons in the substantia nigra, which causes motor symptoms such as dysfunctional bradykinesia, rigidity and tremor. Genetic mutations in Parkinson disease are infrequent and i