Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aneesha, Kohli"'
Autor:
Jana Key, Suzana Gispert, Lieke Koornneef, Esther Sleddens-Linkels, Aneesha Kohli, Sylvia Torres-Odio, Gabriele Koepf, Shady Amr, Marina Reichlmeir, Patrick N. Harter, Andrew Phillip West, Christian Münch, Willy M. Baarends, Georg Auburger
Publikováno v:
Cells, Vol 12, Iss 1, p 52 (2022)
Human Perrault syndrome (PRLTS) is autosomal, recessively inherited, and characterized by ovarian insufficiency with hearing loss. Among the genetic causes are mutations of matrix peptidase CLPP, which trigger additional azoospermia. Here, we analyze
Externí odkaz:
https://doaj.org/article/bfcfed9fb52d4af5857419515812626b
Autor:
Suzana Gispert, Jana Key, Aneesha Kohli, Sylvia Torres-Odio, Gabriele Koepf, Shady Amr, Marina Reichlmeir, Patrick N. Harter, A. Phillip West, Christian Münch, Georg Auburger
Human Perrault syndrome (PRLTS) is defined by autosomal recessive inheritance with primary ovarian insufficiency and early hearing loss. Most PRLTS disease proteins modulate mitochondrial transcription or translation. Among the genetic causes are Clp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23671b83d76833f8293951724ed4a250
https://doi.org/10.20944/preprints202205.0033.v1
https://doi.org/10.20944/preprints202205.0033.v1
Autor:
Aneesha, Kohli, Lucie, Sauerhering, Sarah K, Fehling, Kevin, Klann, Helmut, Geiger, Stephan, Becker, Benjamin, Koch, Patrick C, Baer, Thomas, Strecker, Christian, Münch
Publikováno v:
Life science alliance. 5(5)
Acute kidney injury is associated with mortality in COVID-19 patients. However, host cell changes underlying infection of renal cells with SARS-CoV-2 remain unknown and prevent understanding of the molecular mechanisms that may contribute to renal pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39dc0c45ee944ced2af04ce230f368e5
https://pubmed.ncbi.nlm.nih.gov/35110370
https://pubmed.ncbi.nlm.nih.gov/35110370
Autor:
Antonia Maletzko, Juliana Heidler, Clea Bárcena, Yuanjiu Lei, Sylvia Torres-Odio, Aneesha Kohli, Suzana Gispert, Georg Auburger, Jana Key, Carlos López-Otín, A. Phillip West, Ilka Wittig, Christian Münch
Publikováno v:
Scopus
RUO: Repositorio Institucional de la Universidad de Oviedo
Universidad de Oviedo (UNIOVI)
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Neurogenetics
RUO: Repositorio Institucional de la Universidad de Oviedo
Universidad de Oviedo (UNIOVI)
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Neurogenetics
Human RNF213, which encodes the protein mysterin, is a known susceptibility gene for moyamoya disease (MMD), a cerebrovascular condition with occlusive lesions and compensatory angiogenesis. Mysterin mutations, together with exposure to environmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98d244c8c2208b7129cb00d6101e45f
http://hdl.handle.net/10651/56676
http://hdl.handle.net/10651/56676
Autor:
Jana Key, Carlos López-Otín, Clea Bárcena, Aneesha Kohli, Juliana Heidler, Georg Auburger, Ilka Wittig
Research on healthy aging shows that lifespan reductions are often caused by mitochondrial dysfunction. Thus, it is very interesting that the deletion of mitochondrial matrix peptidase LonP1 was observed to abolish embryogenesis, while deletion of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23fe6fff387d28a7c7e206e98b6b1722
https://doi.org/10.20944/preprints201907.0144.v1
https://doi.org/10.20944/preprints201907.0144.v1