Growth Factor Preconditioning Increases the Function of Diabetes-Impaired Mesenchymal Stem Cells von Khan, Mohsin, Akhtar, Shoaib, Mohsin, Sadia, N. Khan, Shaheen, Riazuddin, Sheikh

Volltext

Mesenchymal stem cells and Interleukin-6 attenuate liver fibrosis in mice von Nasir, Ghazanfar Ali, Mohsin, Sadia, Khan, Mohsin, Shams, Sulaiman, Ali, Gibran, Khan, Shaheen N, Riazuddin, Sheikh

Volltext

Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse von Yousaf, Rizwan, Gu, Chunfang, Ahmed, Zubair M, Khan, Shaheen N, Friedman, Thomas B, Riazuddin, Sheikh, Shears, Stephen B, Riazuddin, Saima

Volltext

Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities von Choudhery, Mahmood Saba, Khan, Mohsin, Mahmood, Ruhma, Mehmood, Azra, Khan, Shaheen N., Riazuddin, Sheikh

Volltext

Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice von Khan, Mohsin, Mohsin, Sadia, Khan, Shaheen N., Riazuddin, Sheikh

Volltext

Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis von Ali, Gibran, Mohsin, Sadia, Khan, Mohsin, Nasir, Ghazanfar Ali, Shams, Sulaiman, Khan, Shaheen N, Riazuddin, Sheikh

Volltext

Tricellulin Is a Tight-Junction Protein Necessary for Hearing von Riazuddin, Saima, Ahmed, Zubair M., Fanning, Alan S., Lagziel, Ayala, Kitajiri, Shin-ichiro, Ramzan, Khushnooda, Khan, Shaheen N., Chattaraj, Parna, Friedman, Penelope L., Anderson, James M., Belyantseva, Inna A., Forge, Andrew, Riazuddin, Sheikh, Friedman, Thomas B.

Volltext

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 von Rehman, Atteeq Ur, Morell, Robert J., Belyantseva, Inna A., Khan, Shahid Y., Boger, Erich T., Shahzad, Mohsin, Ahmed, Zubair M., Riazuddin, Saima, Khan, Shaheen N., Riazuddin, Sheikh, Friedman, Thomas B.

Volltext

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma von Ali, Manir, McKibbin, Martin, Booth, Adam, Parry, David A., Jain, Payal, Riazuddin, S. Amer, Hejtmancik, J. Fielding, Khan, Shaheen N., Firasat, Sabika, Shires, Mike, Gilmour, David F., Towns, Katherine, Murphy, Anna-Louise, Azmanov, Dimitar, Tournev, Ivailo, Cherninkova, Sylvia, Jafri, Hussain, Raashid, Yasmin, Toomes, Carmel, Craig, Jamie, Mackey, David A., Kalaydjieva, Luba, Riazuddin, Sheikh, Inglehearn, Chris F.

Volltext

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86 von Rehman, Atteeq U., Santos-Cortez, Regie Lyn P., Morell, Robert J., Drummond, Meghan C., Ito, Taku, Lee, Kwanghyuk, Khan, Asma A., Basra, Muhammad Asim R., Wasif, Naveed, Ayub, Muhammad, Ali, Rana A., Raza, Syed I., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael, Riazuddin, Saima, Billington, Neil, Khan, Shaheen N., Friedman, Penelope L., Griffith, Andrew J., Ahmad, Wasim, Riazuddin, Sheikh, Leal, Suzanne M., Friedman, Thomas B.

Volltext

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1 von Khan, Shahid Y., Vasanth, Shivakumar, Kabir, Firoz, Gottsch, John D., Khan, Arif O., Chaerkady, Raghothama, Lee, Mei-Chong W., Leitch, Carmen C., Ma, Zhiwei, Laux, Julie, Villasmil, Rafael, Khan, Shaheen N., Riazuddin, Sheikh, Akram, Javed, Cole, Robert N., Talbot, C. Conover, Pourmand, Nader, Zaghloul, Norann A., Hejtmancik, J. Fielding, Riazuddin, S. Amer

Volltext

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts von Irum, Bushra, Khan, Shahid Y, Ali, Muhammad, Kaul, Haiba, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Nadeem, Raheela, Khan, Arif O, Al Obaisi, Saif, Naeem, Muhammad Asif, Nasir, Idrees A, Khan, Shaheen N, Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O, Riazuddin, S Amer

Volltext

Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families von Li, Lin, Chen, Yabin, Jiao, Xiaodong, Jin, Chongfei, Jiang, Dan, Tanwar, Mukesh, Ma, Zhiwei, Huang, Li, Ma, Xiaoyin, Sun, Wenmin, Chen, Jianjun, Ma, Yan, M'hamdi, Oussama, Govindarajan, Gowthaman, Cabrera, Patricia E, Li, Jiali, Gupta, Nikhil, Naeem, Muhammad Asif, Khan, Shaheen N, Riazuddin, Sheikh, Akram, Javed, Ayyagari, Radha, Sieving, Paul A, Riazuddin, S Amer, Hejtmancik, J Fielding

Volltext

A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa von Riazuddin, S. Amer, Iqbal, Muhammad, Wang, Yue, Masuda, Tomohiro, Chen, Yuhng, Bowne, Sara, Sullivan, Lori S., Waseem, Naushin H., Bhattacharya, Shomi, Daiger, Stephen P., Zhang, Kang, Khan, Shaheen N., Riazuddin, Sheikh, Hejtmancik, J. Fielding, Sieving, Paul A., Zack, Donald J., Katsanis, Nicholas

Volltext

An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans von Jaworek, Thomas J, Richard, Elodie M, Ivanova, Anna A, Giese, Arnaud P J, Choo, Daniel I, Khan, Shaheen N, Riazuddin, Sheikh, Kahn, Richard A, Riazuddin, Saima

Volltext

Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts von Irum, Bushra, Khan, Shahid Y, Ali, Muhammad, Daud, Muhammad, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Iqbal, Hira, Khan, Arif O, Al Obaisi, Saif, Naeem, Muhammad Asif, Nasir, Idrees A, Khan, Shaheen N, Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O, Riazuddin, S Amer

Volltext

Mesenchymal Stem Cells Pretreated with HGF and FGF4 Can Reduce Liver Fibrosis in Mice von Khan, Mohsin, Nasir, Ghazanfar Ali, Mohsin, Sadia, Shams, Sulaiman, Khan, Shaheen N.

Volltext

Adipose stem cells differentiated chondrocytes regenerate damaged cartilage in rat model of osteoarthritis von Latief, Noreen, Raza, Fahad Ali, Bhatti, Fazal-Ur-Rehman, Tarar, Moazzam Nazir, Khan, Shaheen N., Riazuddin, Sheikh

Volltext

Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment von Masoud, Muhammad Shareef, Anwar, Sanam Saiqa, Afzal, Muhammad Zeeshan, Mehmood, Azra, Khan, Shaheen N, Riazuddin, Sheikh

Volltext

Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts von Irum, Bushra, Khan, Shahid Y, Ali, Muhammad, Daud, Muhammad, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Iqbal, Hira, Khan, Arif O, Obaisi, Saif Al, Naeem, Muhammad Asif, Nasir, Idrees A, Khan, Shaheen N, Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O, Riazuddin, S Amer

Volltext