Zobrazeno 1 - 10
of 542
pro vyhledávání: '"Baran, E. A."'
Publikováno v:
In Revista de Gastroenterología de México (English Edition) January-March 2024 89(1):19-24
Publikováno v:
In Revista de Gastroenterología de México January-March 2024 89(1):19-24
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
The human Usher syndrome (USH) is the most common form of a sensory hereditary ciliopathy characterized by progressive vision and hearing loss. Mutations in the genes ADGRV1 and CIB2 have been associated with two distinct sub-types of USH, namely, US
Externí odkaz:
https://doaj.org/article/b051c4e7f75a4dd8b3aa8b33d9c8634b
Autor:
Linnert, Joshua1 (AUTHOR), Güler, Baran E.1 (AUTHOR), Krzysko, Jacek1 (AUTHOR), Wolfrum, Uwe1 (AUTHOR) wolfrum@uni-mainz.de
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. Oct2023, Vol. 133 Issue 4, p313-330. 18p.
Autor:
Güler, Baran E.1 (AUTHOR), Linnert, Joshua1 (AUTHOR), Wolfrum, Uwe1 (AUTHOR) wolfrum@uni-mainz.de
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. Oct2023, Vol. 133 Issue 4, p301-312. 12p.
Autor:
Kusuluri, Deva K., Güler, Baran E., Knapp, Barbara, Horn, Nicola, Boldt, Karsten, Ueffing, Marius, Aust, Gabriela, Wolfrum, Uwe
Publikováno v:
In iScience 23 April 2021 24(4)
Publikováno v:
In Journal of Medical Mycology March 2021 31(1)
Autor:
Knapp, Barbara, Roedig, Jens, Roedig, Heiko, Krzysko, Jacek, Horn, Nicola, Güler, Baran E., Kusuluri, Deva Krupakar, Yildirim, Adem, Boldt, Karsten, Ueffing, Marius, Liebscher, Ines, Wolfrum, Uwe
The very large G-protein-coupled receptor 1 (VLGR1/ADGRV1) is the largest member of the adhesion G-protein-coupled receptor (ADGR) family. Mutations in VLGR1/ADGRV1 cause human Usher syndrome (USH), a form of hereditary deaf-blindness, and have been
Externí odkaz:
https://ul.qucosa.de/id/qucosa%3A87161
https://ul.qucosa.de/api/qucosa%3A87161/attachment/ATT-0/
https://ul.qucosa.de/api/qucosa%3A87161/attachment/ATT-0/
Publikováno v:
STAR Protocols, Vol 2, Iss 4, Pp 100954- (2021)
Summary: Primary astrocytes have gained attention as an important model for in vitro biological and biochemical research in the last decades. In this protocol, we describe a fast and cost-effective technique for isolating, culturing, and maintaining
Externí odkaz:
https://doaj.org/article/741d2086c119436caa30703ee0d3c7af
Autor:
Deva K. Kusuluri, Baran E. Güler, Barbara Knapp, Nicola Horn, Karsten Boldt, Marius Ueffing, Gabriela Aust, Uwe Wolfrum
Publikováno v:
iScience, Vol 24, Iss 4, Pp 102283- (2021)
Summary: VLGR1 (very large G protein-coupled receptor-1) is by far the largest adhesion G protein-coupled receptor in humans. Homozygous pathologic variants of VLGR1 cause hereditary deaf blindness in Usher syndrome 2C and haploinsufficiency of VLGR1
Externí odkaz:
https://doaj.org/article/232b824b2ea04d888eca98f77fd93557