Zobrazeno 1 - 10
of 198
pro vyhledávání: '"Zubair A Ahmed"'
Autor:
Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A. Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A. Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M. Ahmed, Sheikh Riazuddin, Saima Riazuddin
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-13 (2024)
Abstract Microtubule associated proteins (MAPs) are widely expressed in the central nervous system, and have established roles in cell proliferation, myelination, neurite formation, axon specification, outgrowth, dendrite, and synapse formation. We r
Externí odkaz:
https://doaj.org/article/50e5cd7c61094b2f8a582125939521fc
Autor:
Ayesha Yousaf, Sairah Yousaf, Asra S. Shabbir, Rafia Yousaf, Saima Riazuddin, Rehan S. Shaikh, Regie Lyn P. Santos‐Cortez, Zubair M. Ahmed
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 9, Pp n/a-n/a (2024)
Abstract Background Otitis media (OM) is the most frequent and complex middle ear condition with multifactorial etiology including genetic predisposition. OM depicts a variable clinical spectrum, leading to speech, developmental delay, and hearing lo
Externí odkaz:
https://doaj.org/article/1e03f75a035c448caef401d07f158078
Autor:
Abbas, Shajar, Un Nisa, Zaib, Nazar, Mudassar, Metwally, Ahmed Sayed M., Kędzia, Krzysztof, Zubair Jan, Ahmed, Kamolova, Nargiza
Publikováno v:
In International Journal of Thermal Sciences January 2025 207
Autor:
Patel, Bilal Ahmed Alim1 (AUTHOR) patelbilal4862@gmail.com, Shaikh, Zubair Saghir Ahmed1 (AUTHOR) patelbilal4862@gmail.com, Patil, Sulbha G.1 (AUTHOR), Pulipati, Sowjanya2 (AUTHOR) sowjypulipati@gmail.com
Publikováno v:
Biology & Life Sciences Forum. 2023, Vol. 24, p3. 7p.
Autor:
Yilan Zhen, Carlie L. Cullen, Raphael Ricci, Benjamin S. Summers, Sakina Rehman, Zubair M. Ahmed, Antoinette Y. Foster, Ben Emery, Robert Gasperini, Kaylene M. Young
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-21 (2022)
Protocadherin 15 promotes lamellipodial and filopodial dynamics in oligodendrocyte progenitor cells by regulating Cdc42-Arp2/3 activity, but also suppresses ERK1/2 phosphorylation to reduce proliferation.
Externí odkaz:
https://doaj.org/article/5c6fb3dbd66a477395c3c0828c084902
Publikováno v:
Biology and Life Sciences Forum, Vol 24, Iss 1, p 3 (2023)
In several cultures, black cumin, also known as Nigella sativa, has long been used medicinally. Recent research has revealed that this plant has potent anti-inflammatory and antioxidant qualities, making it a possible treatment for several medical co
Externí odkaz:
https://doaj.org/article/318b16c724a8419982d5b79f5226f2e9
Autor:
Saumil Sethna, Patrick A. Scott, Arnaud P. J. Giese, Todd Duncan, Xiaoying Jian, Sheikh Riazuddin, Paul A. Randazzo, T. Michael Redmond, Steven L. Bernstein, Saima Riazuddin, Zubair M. Ahmed
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-19 (2021)
Age-related macular degeneration (AMD) has been connected to deficits in autophagy. Here, the authors demonstrate, in mice and dry-AMD patient samples, that calcium and integrin binding protein 2 (CIB2) regulates Rheb-mTORC1 signaling axis, and subse
Externí odkaz:
https://doaj.org/article/28f9c426a95d413a8bcf70e1675378bc
Publikováno v:
Materials Proceedings, Vol 14, Iss 1, p 57 (2023)
A frequent type of hair loss that affects both men and women, androgenetic alopecia is indicated by the gradual miniaturization of hair follicles, which results in thinner and shorter hair growth cycles. Despite the availability of various treatment
Externí odkaz:
https://doaj.org/article/ff88d5557d824db7bb70e1d2b3fc5536
Autor:
Saumil Sethna, Wadih M Zein, Sehar Riaz, Arnaud PJ Giese, Julie M Schultz, Todd Duncan, Robert B Hufnagel, Carmen C Brewer, Andrew J Griffith, T Michael Redmond, Saima Riazuddin, Thomas B Friedman, Zubair M Ahmed
Publikováno v:
eLife, Vol 10 (2021)
Usher syndrome type I (USH1) is characterized by deafness, vestibular areflexia, and progressive retinal degeneration. The protein-truncating p.Arg245* founder variant of PCDH15 (USH1F) has an ~2% carrier frequency amongst Ashkenazi Jews accounts for
Externí odkaz:
https://doaj.org/article/b6069badb6b14498bff5ec71588e5683
Autor:
Muhammad Rashid, Sairah Yousaf, Shakeel A. Sheikh, Zureesha Sajid, Asra S. Shabbir, Tasleem Kausar, Nabeela Tariq, Muhammad Usman, Rehan S. Shaikh, Muhammad Ali, Shazia A. Bukhari, Ali M. Waryah, Muhammad Qasim, Saima Riazuddin, Zubair M. Ahmed
Publikováno v:
Molecular Vision, Vol 25, Iss 1, Pp 144-154 (2019)
Purpose: Primary congenital glaucoma (PCG) is a clinically and genetically heterogeneous disease. The present study was undertaken to find the genetic causes of PCG segregating in 36 large consanguineous Pakistani families. Methods: Ophthalmic exa
Externí odkaz:
https://doaj.org/article/b5f6a5b6d40842db87f7126c07225a1f