Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Eszter Vamos"'
Autor:
Kitti Bruszt, Orsolya Horvath, Katalin Ordog, Szilard Toth, Kata Juhasz, Eszter Vamos, Katalin Fekete, Ferenc Gallyas, Kalman Toth, Robert Halmosi, Laszlo Deres
Publikováno v:
PLoS ONE, Vol 19, Iss 11, p e0310394 (2024)
Mitochondria form a dynamic network in cells, regulated by the balance between mitochondrial fusion and fission. The inhibition of mitochondrial fission can have positive effects in acute ischemic/reperfusion injury models by preventing the fall in m
Externí odkaz:
https://doaj.org/article/1d412bb4e21a4b9ca093a2e6e47a9e5f
Autor:
Ailsa J. McKay, Laura H. Gunn, Thirunavukkarasu Sathish, Eszter Vamos, Manjula Nugawela, Azeem Majeed, German Molina, Sobha Sivaprasad
Publikováno v:
BMC Medicine, Vol 19, Iss 1, Pp 1-10 (2021)
Abstract Background The associations between England’s incentivised primary care-based diabetes prevention activities and hard clinical endpoints remain unclear. We aimed to examine the associations between attainment of primary care indicators and
Externí odkaz:
https://doaj.org/article/b19636f94db043f2841e9a331766a642
Autor:
Heidi Lai, Angelica Sharma, Kiara Chang, Mansour Sharabiani, Alex Bottle, Jonathan Valabhji, Lefkos Middleton, Azeem Majeed, Christopher Millett, Eszter Vamos
Publikováno v:
SSM Annual Scientific Meeting.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcb51292a4ec0b82c1f1c81bc5edde92
https://doi.org/10.1136/jech-2022-ssmabstracts.2
https://doi.org/10.1136/jech-2022-ssmabstracts.2
Autor:
Eszter Vamos, Harvey A. Greisman, Hye Son Yi, Alex Kentsis, Daniel E. Sabath, Vijay G. Sankaran, Michaël Bender
Publikováno v:
The Journal of Molecular Diagnostics. 18:92-99
Thalassemia is among the most common genetic diseases worldwide. α-Thalassemia is usually caused by deletion of one or more of the duplicated HBA genes on chromosome 16. In contrast, most β-thalassemia results from point mutations that decrease or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc80e0ea2cbe610ad2cf66527a80985b
https://doi.org/10.1016/j.jmoldx.2015.07.011
https://doi.org/10.1016/j.jmoldx.2015.07.011
Publikováno v:
Europe PubMed Central
We assessed the reliability of a method designed for common electron-impact GC-MS systems to determine in a single run most organic acids and glycine conjugates of clinical interest in amniotic fluid. Suitable sensitivity was achieved by dividing the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d1124a2b3a9c307957c5385fcacdfe4
https://doi.org/10.1023/b:boli.0000042981.52186.a9
https://doi.org/10.1023/b:boli.0000042981.52186.a9
Autor:
Eszter Vámos, Nikoletta Kálmán, Eva Maria Sturm, Barsha Baisakhi Nayak, Julia Teppan, Viola Bagóné Vántus, Dominika Kovács, Lilla Makszin, Tamás Loránd, Ferenc Gallyas, Balázs Radnai
Publikováno v:
Antioxidants, Vol 12, Iss 10, p 1790 (2023)
Macrophage polarization is highly involved in autoimmunity. M1 polarized macrophages drive inflammation and undergo metabolic reprogramming, involving downregulation of mitochondrial energy production and acceleration of glycolysis. Macrophage migrat
Externí odkaz:
https://doaj.org/article/c0c9d5b9aad4471c81497d27643fe5b2
Publikováno v:
American Journal of Medical Genetics. 93:244-249
Most cases with Kabuki syndrome (KS) were reported sporadically. Recently, a few familial cases of KS were reported. This report provides further evidence that the KS is inherited as a dominant trait with variable expressivity. The proposita is an 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d793ed5915b3b074ff96ffd5e509a4f7
https://doi.org/10.1002/1096-8628(20000731)93:3<244::aid-ajmg17>3.0.co
https://doi.org/10.1002/1096-8628(20000731)93:3<244::aid-ajmg17>3.0.co
Publikováno v:
Ghent University Academic Bibliography
A boy with features suggesting the diagnosis of Wiedemann-Rautenstrauch syndrome (WRS) or neonatal progeroid syndrome is presented. Abnormal findings included a generalized virtual absence of subcutaneous fat, sparse scalp hair, prominence of veins a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d9220f73fc8eaa1869cd347e38a9097
https://doi.org/10.1097/00019605-199707000-00004
https://doi.org/10.1097/00019605-199707000-00004
Autor:
János Garai, Marcell Krekó, László Őrfi, Péter Balázs Jakus, Zoltán Rumbus, Patrik Kéringer, András Garami, Eszter Vámos, Dominika Kovács, Viola Bagóné Vántus, Balázs Radnai, Tamás Lóránd
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1356-1368 (2021)
Macrophage migration inhibitory factor (MIF) is a pro-inflammatory cytokine playing crucial role in immunity. MIF exerts a unique tautomerase enzymatic activity that has relevance concerning its multiple functions and its small molecule inhibitors ha
Externí odkaz:
https://doaj.org/article/99c9586e388a44fd96582e44a894d6e8
Autor:
Stephen W. Scherer, Angela M. Christiano, Renata Rizzo, Anja Raams, Erik G. Puffenberger, Julio C. Salas-Alanis, Nicolaas G. J. Jaspers, Ulpu Saarialho-Kere, Jacques S. Beckmann, Jeffrey R. MacDonald, Charles E. Jackson, Clifford M. Les, Amalia Martinez-Mir, Yan Ren, Daniela Amann, Kazuhiko Nakabayashi, Nili Avidan, Simone Gentles, Eszter Vamos, Eric Seboun
Publikováno v:
American Journal of Human Genetics, 76(3), 510-516. Cell Press
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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7 páginas, 2 figuras, 1 tabla.
We have identified C7orf11, which localizes to the nucleus and is expressed in fetal hair follicles, as the first disease gene for nonphotosensitive trichothiodystrophy (TTD). C7orf11 maps to chromosome 7p14, and
We have identified C7orf11, which localizes to the nucleus and is expressed in fetal hair follicles, as the first disease gene for nonphotosensitive trichothiodystrophy (TTD). C7orf11 maps to chromosome 7p14, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f1ea1daef4dd268316977f47826a9b
https://pure.eur.nl/en/publications/5c612142-d8ee-4686-b6fc-438fbd31baeb
https://pure.eur.nl/en/publications/5c612142-d8ee-4686-b6fc-438fbd31baeb
