Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mustafa, Khokha"'
Autor:
Bilal Azab, Dunia Aburizeg, Sherin T. Shaaban, Weizhen Ji, Lina Mustafa, Nooredeen Jamal Isbeih, Amal Saleh Al-Akily, Hashim Mohammad, Lauren Jeffries, Mustafa Khokha, Saquib A. Lakhani, Iyad Al-Ammouri
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Pediatric cardiomyopathies are mostly attributed to variants in sarcomere-related genes. Unfortunately, the genetic architecture of pediatric cardiomyopathies has never been previously studied in Jordan. We sought to uncover the genetic land
Externí odkaz:
https://doaj.org/article/5f67b5f0f24440549110a09f99d7af09
Autor:
Youying Mao, Ronen Schneider, Peter F.M. van der Ven, Marvin Assent, Keerthika Lohanadan, Verena Klämbt, Florian Buerger, Thomas M. Kitzler, Konstantin Deutsch, Makiko Nakayama, Amar J. Majmundar, Nina Mann, Tobias Hermle, Ana C. Onuchic-Whitford, Wei Zhou, Nandini Nagarajan Margam, Roy Duncan, Jonathan Marquez, Mustafa Khokha, Hanan M. Fathy, Jameela A. Kari, Sherif El Desoky, Loai A. Eid, Hazem Subhi Awad, Muna Al-Saffar, Shrikant Mane, Richard P. Lifton, Dieter O. Fürst, Shirlee Shril, Friedhelm Hildebrandt
Publikováno v:
Kidney International Reports, Vol 6, Iss 2, Pp 472-483 (2021)
Introduction: Most of the approximately 60 genes that if mutated cause steroid-resistant nephrotic syndrome (SRNS) are highly expressed in the glomerular podocyte, rendering SRNS a “podocytopathy.” Methods: We performed whole-exome sequencing (WE
Externí odkaz:
https://doaj.org/article/dd37eae7f792449e9379ede47e4cb65a
Publikováno v:
The FASEB Journal. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa63bd42d4d3f0e33be9d50343f914cb
https://doi.org/10.1096/fasebj.2022.36.s1.r4889
https://doi.org/10.1096/fasebj.2022.36.s1.r4889
Autor:
Nina N, Brodsky, Oksana, Boyarchuk, Tetyana, Kovalchuk, Tetyana, Hariyan, Andrew, Rice, Weizhen, Ji, Mustafa, Khokha, Saquib, Lakhani, Carrie L, Lucas
Publikováno v:
Journal of human genetics. 65(10)
Two variants in the ubiquitously expressed NHLRC2 gene have been reported to cause a lethal fibrotic cerebropulmonary disease termed fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA) syndrome in three Finnish children. Our objective was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24c2ef19f2ec0b91748f2be057680c32
https://pubmed.ncbi.nlm.nih.gov/32435055
https://pubmed.ncbi.nlm.nih.gov/32435055
Autor:
Robert L. Bacallao, Frank A. Carone, Sakie Nakamura, Mustafa Khokha, Yashpal S. Kanwar, W. J. Nelson
Publikováno v:
Kidney International. 47(3):861-868
Impaired tubulogenesis of cyst-derived cells from autosomal dominant polycystic kidneys. Under appropriate growth factor or hormonal influence, renal epithelial cells cultured in collagen gels form branching tubular elements, reminiscent of metanephr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6abe27502f4253ab3a800839fadc47e8
Autor:
Florencia, del Viso, Mustafa, Khokha
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 917
A spectacular advantage of Xenopus tropicalis is the ease with which diploid embryos can be generated year round. By the simple administration of human chorionic gonadotropin, an investigator can generate many hundreds of synchronized embryos by in v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a454a172ae4ad6f65b5329837610b17
https://pubmed.ncbi.nlm.nih.gov/22956081
https://pubmed.ncbi.nlm.nih.gov/22956081