Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Rizwan Yousaf"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101487- (2024)
Externí odkaz:
https://doaj.org/article/da4a623c356c4df8ab7d04cee7d13309
Autor:
Jorune Balciuniene, Ruby Liu, Lora Bean, Babi Ramesh Reddy Nallamilli, Naga Guruju, Xiangwen Chen-Deutsch, Rizwan Yousaf, Kristina Fura, Eprem Chin, Abhinav Mathur, Zeqiang Ma, Jonathan Carmichael, Christin Collins, Cristina da Silva, Brian Kirmse, Steven Bleyl, Madhuri Hegde
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101618- (2024)
Externí odkaz:
https://doaj.org/article/84b8713922944e74ae4f889c8f3d697e
Autor:
Fen Guo, Ruby Liu, Yinghong Pan, Christin D. Collins, Lora Bean, Babi Ramesh Reddy Nallamilli, Naga Guruju, Xiangwen Chen-Deutsch, Rizwan Yousaf, Ephrem Chin, Cristina da Silva, Abhinav Mathur, Zeqiang Ma, Jorune Balciuniene, Madhuri Hegde
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100425- (2023)
Externí odkaz:
https://doaj.org/article/bb65bd1c873948899aacfe604fed82df
Autor:
Lora Bean, Christin Collins, Fen Guo, Jorune Balciuniene, Xiangwen Chen-Deutsch, Babi Ramesh Reddy Nallamilli, Naga Guruju, Rizwan Yousaf, Kristina Fura, Amber Woodman, Ruby Liu, Jenny Zhang, Kate Liebmann, Julia Gerow, Ephrem Chin, Madhuri Hegde
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100473- (2023)
Externí odkaz:
https://doaj.org/article/5737bda9aefc434aa04197bf5333f2f5
Autor:
Jorune Balciuniene, Ruby Liu, Christin Collins, Lora Bean, Fen Guo, Babi Ramesh Reddy Nallamilli, Naga Guruju, Xiangwen Chen-Deutsch, Rizwan Yousaf, Kristina Fura, Ephrem Chin, Cristina da Silva, Abhinav Mathur, Zeqiang Ma, Madhuri Hegde
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100472- (2023)
Externí odkaz:
https://doaj.org/article/837911eed0a74417b39b5fc38ef7b6cb
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 5, Pp 1544-1547 (2021)
Objective: To determine frequency of vitamin D deficiency in patients presenting with fibromyalgia and its association with various factors. Study Design: Cross sectional study. Place and Duration of Study: Medicine department, Pak Emirates Mil
Externí odkaz:
https://doaj.org/article/312d9a49d7e34d768a80b561ba6a5471
Autor:
Amrita A Iyer, Ishwar Hosamani, John D Nguyen, Tiantian Cai, Sunita Singh, Melissa M McGovern, Lisa Beyer, Hongyuan Zhang, Hsin-I Jen, Rizwan Yousaf, Onur Birol, Jenny J Sun, Russell S Ray, Yehoash Raphael, Neil Segil, Andrew K Groves
Publikováno v:
eLife, Vol 11 (2022)
Reprogramming of the cochlea with hair-cell-specific transcription factors such as ATOH1 has been proposed as a potential therapeutic strategy for hearing loss. ATOH1 expression in the developing cochlea can efficiently induce hair cell regeneration
Externí odkaz:
https://doaj.org/article/4cbcd933e07d46508ec37fe3ede0949c
Autor:
Rizwan Yousaf, Qinghang Meng, Robert B. Hufnagel, Ying Xia, Chandrakala Puligilla, Zubair M. Ahmed, Saima Riazuddin
Publikováno v:
Disease Models & Mechanisms, Vol 8, Iss 12, Pp 1543-1553 (2015)
MAP3K1 is a serine/threonine kinase that is activated by a diverse set of stimuli and exerts its effect through various downstream effecter molecules, including JNK, ERK1/2 and p38. In humans, mutant alleles of MAP3K1 are associated with 46,XY sex re
Externí odkaz:
https://doaj.org/article/e2732dad116f4b91be1430b4adbc5deb
Autor:
Rizwan Yousaf, Chunfang Gu, Zubair M Ahmed, Shaheen N Khan, Thomas B Friedman, Sheikh Riazuddin, Stephen B Shears, Saima Riazuddin
Publikováno v:
PLoS Genetics, Vol 14, Iss 3, p e1007297 (2018)
Autosomal recessive nonsyndromic hearing loss is a genetically heterogeneous disorder. Here, we report a severe-to-profound sensorineural hearing loss locus, DFNB100 on chromosome 5q13.2-q23.2. Exome enrichment followed by massive parallel sequencing
Externí odkaz:
https://doaj.org/article/82cbaa41f0b04304a24ab3821e971473
Autor:
Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E. Turriff, Keith Pelstring, Bin Guan, Amelia Naik, Andrew J. Griffith, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Gordon A. Awandare, Robert J. Morell, Ekaterini Tsilou, Amanda G. Noyes, Laura A. G. Sulmonte, Ambroise Wonkam, Isabelle Schrauwen, Suzanne M. Leal, Hela Azaiez, Carmen C. Brewer, Sheikh Riazuddin, Robert B. Hufnagel, Michael Hoa, Wadih M. Zein, J. Karl de Dios, Thomas B. Friedman
Publikováno v:
Clinical Genetics. 103:699-703
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fa28c57eb07bd63d0020e5fb71c72c4
https://doi.org/10.1111/cge.14312
https://doi.org/10.1111/cge.14312