Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lilas Batool"'
Autor:
Lilas Batool, Olha Storozhuk, Constanze Raab, Christien Madlen Beez, Mareike Selig, Anja Harder, Andreas Kurtz
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103184- (2023)
We describe the generation of two human induced pluripotent stem cell (iPSC) lines derived from peripheral blood mononuclear cells (PBMCs) using a non-integrative episomal reprogramming strategy. The first cell line was derived from a NF1 patient wit
Externí odkaz:
https://doaj.org/article/368bfea34a37415a85d2a9998d4fc6d2
Autor:
Lilas Batool, Constanze Raab, Christien Madlen Beez, Andreas Kurtz, Maik Gollasch, Bella Rossbach
Publikováno v:
Stem Cell Research, Vol 69, Iss , Pp 103071- (2023)
Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic disorder of adults, characterized by uncontrolled cysts formation that causes a gradual impairment of kidney function. We generated a human induced pluripotent stem cell (hiPSC)
Externí odkaz:
https://doaj.org/article/5ec4561cb9b3400c8e8c12e12a03d31d
Autor:
Lilas Batool, Constanze Raab, Christien Madlen Beez, Krithika Hariharan, Andreas Kurtz, Maik Gollasch, Bella Rossbach
Publikováno v:
Stem Cell Research, Vol 69, Iss , Pp 103070- (2023)
Individuals with transient reception potential cation channel 6 (TRPC6) mutation have variable phenotypes, ranging from healthy carriers to focal segmental glomerulosclerosis (FSGS). Human induced pluripotent stem cell (hiPSC) line was generated from
Externí odkaz:
https://doaj.org/article/7899c10de37e479d980388ae43476fd9
Autor:
Khushnooda Ramzan, Sibtain Afzal, Lilas Batool, Abdul Wali, Abrar Hussain, Ambreen Ijaz, Ajab Gul, Sulman Basit, Jamil Ahmad
Publikováno v:
Congenital Anomalies. 59:18-21
Xeroderma pigmentosum (XP) is a rare autosomal recessive skin disorder characterized by hyperpigmentation, premature skin aging, ocular and cutaneous photosensitivity, and increased risk of skin carcinoma. We investigated seven consanguineous XP fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f4a66b53b322a2b2a03c89033ee9102
https://doi.org/10.1111/cga.12281
https://doi.org/10.1111/cga.12281
Autor:
Ambreen, Ijaz, Sulman, Basit, Ajab, Gul, Lilas, Batool, Abrar, Hussain, Sibtain, Afzal, Khushnooda, Ramzan, Jamil, Ahmad, Abdul, Wali
Publikováno v:
Congenital anomalies. 59(1)
Xeroderma pigmentosum (XP) is a rare autosomal recessive skin disorder characterized by hyperpigmentation, premature skin aging, ocular and cutaneous photosensitivity, and increased risk of skin carcinoma. We investigated seven consanguineous XP fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88986bb539f26020cbbe99bd516670db
https://pubmed.ncbi.nlm.nih.gov/29569758
https://pubmed.ncbi.nlm.nih.gov/29569758