Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ammara, Jabeen"'
Publikováno v:
The Healer Journal of Physiotherapy and Rehabilitation Sciences. 3:415-422
Background: It can be very stressful for students to be under constant pressure to succeed in becoming highly qualified healthcare professionals. Postgraduate and professional students were found to experience higher levels of stress than usual when
Autor:
Ammara Jabeen, Qaisar Mansoor, Tayyaba Zainab, Ammad Ahmad Farooqi, Mazhar Qayyum, Aqsa Mansha, Arifa Shakeel, Muhammad Sheeraz Ahmad
Publikováno v:
Molecular biology reports. 49(6)
Transforming growth factor beta (TGF-β) superfamily has key role in cell proliferation which leads to tumor promoting activities at metastatic stage of cancer. Inhibition of transforming growth factor beta receptor (TGFβR) signaling pathway can pro
Autor:
Nauman, Aziz, Abdul, Sami, Ammara, Jabeen, Muhammad, Gulfraz, Rahmatullah, Qureshi, Tanveer, Ibrahim, Ammad Ahmad, Farooqi, S M Saqlan, Naqvi, M Sheeraz, Ahmad
Publikováno v:
Pakistan journal of pharmaceutical sciences. 33(5)
Medicinal plants are long been used for pharmaceutical and cosmetic industry. Among medicinal plants, Polygonum amplexicaule of family polygonaceae has traditional use in medicines and skin care. P. amplexicaule belongs to genus Polygonum that contai
Autor:
Muhammad Sheeraz Ahmad, Arshad Islam, Sana Shamshad, Salma Batool, Azka Noureen, Warda Ahmed, Ammara Jabeen, Tayyaba Zainab, Maryam Shahid
Publikováno v:
Biochemistry of Drug Resistance ISBN: 9783030763190
Neurological disorders are the major health problem worldwide and expected to grow exponentially in coming years. One of the most challenging clinical aspect of neurological disorders is the development of resistance towards drugs in clinics. Failure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07a8f15e770f5a5ba5e9a2c525a94fac
https://doi.org/10.1007/978-3-030-76320-6_9
https://doi.org/10.1007/978-3-030-76320-6_9
Publikováno v:
African Journal of Biotechnology; Vol 12, No 16 (2013)
LAH 2 is a type of autosomal recessive hypotrichosis that affect hairs, eyebrows, scalp and eyelashes. Mutations in Lipase H gene result in LAH 2. Changes that result from mutation on physiochemical properties, post-translational modifications, funct