Zobrazeno 1 - 10
of 2 007
pro vyhledávání: '"GALT"'
Autor:
Zhang, Pingting1
Publikováno v:
Scottish Literary Review. Autumn/Winter2022, Vol. 14 Issue 2, p1-20. 20p.
Publikováno v:
Drug Design, Development and Therapy, Vol Volume 18, Pp 3415-3428 (2024)
Jonathan Barratt,1 Jens Kristensen,2 Christian Pedersen,2 Markus Jerling3 1College of Life Sciences, University of Leicester, Leicester, UK; 2Calliditas Therapeutics AB, Stockholm, Sweden; 3Markus Jerling Consulting AB, Stockholm, SwedenCorrespondenc
Externí odkaz:
https://doaj.org/article/ab32ce7951d44313b8dfa5c98f8a1ed7
Autor:
Linley Mangini, Roger Lawrence, Manuel E. Lopez, Timothy C. Graham, Christopher R. Bauer, Hang Nguyen, Cheng Su, John Ramphal, Brett E. Crawford, Tom A. Hartl
Publikováno v:
JIMD Reports, Vol 65, Iss 4, Pp 280-294 (2024)
Abstract Classic galactosemia (CG) arises from loss‐of‐function mutations in the Galt gene, which codes for the enzyme galactose‐1‐phosphate uridylyltransferase (GALT), a central component in galactose metabolism. The neonatal fatality associ
Externí odkaz:
https://doaj.org/article/681f476298fc43008be14cb90904e903
Autor:
Natalija Jonić, Ivan Koprivica, Stavroula G. Kyrkou, Vasileios-Panagiotis Bistas, Christos Chatzigiannis, Nataša Radulović, Ivan Pilipović, Andjelina Jovanović, Milan B. Jovanović, Mirjana Dimitrijević, Andreas G. Tzakos, Ivana Stojanović
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Type 1 diabetes (T1D) is an autoimmune disease with a strong chronic inflammatory component. One possible strategy for the treatment of T1D is to stimulate the regulatory arm of the immune response, i.e. to promote the function of tolerogenic dendrit
Externí odkaz:
https://doaj.org/article/11b51184e3184bd1b78ab93ef5a4d033
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Galactosemia is an autosomal recessive disorder resulting from an enzyme defect in the galactose metabolic pathway. The most severe manifestation of classic galactosemia is caused by galactose-1-phosphate uridylyltransferase (GALT
Externí odkaz:
https://doaj.org/article/360a55cc99bd4b19938c2362c7edcda8
Publikováno v:
JIMD Reports, Vol 65, Iss 2, Pp 110-115 (2024)
Abstract Classical galactosemia (CG) is an autosomal recessive disorder of galactose metabolism. Despite early initiation of a galactose‐restricted diet, patients develop long‐term complications including cognitive impairment. There is an ongoing
Externí odkaz:
https://doaj.org/article/b62be939fa8541ff82ff87261d76a400
Publikováno v:
International Journal of Contemporary Hospitality Management, 2022, Vol. 36, Issue 2, pp. 524-542.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/IJCHM-03-2022-0403
Autor:
Isaac Rosado-Sánchez, Inés Herrero-Fernández, Salvador Sobrino, Ana E. Carvajal, Miguel Genebat, Laura Tarancón-Díez, María Carmen Garcia-Guerrero, María Carmen Puertas, Rocío M. de Pablos, Rocío Ruiz, Javier Martinez-Picado, Manuel Leal, Yolanda M. Pacheco
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 56, Iss 6, Pp 1129-1138 (2023)
Background: Blood OX40-expressing CD4 T-cells from antiretroviral (ART)-treated people living with HIV (PWH) were found to be enriched for clonally-expanded HIV sequences, hence contributing to the HIV reservoir. OX40-OX40L is also a checkpoint regul
Externí odkaz:
https://doaj.org/article/6a42bf8683cc4f4594a259ba027a4f58
Autor:
Nihal Almenabawy, Shalini Bahl, Alyssa-Lyn Ostlund, Shailly Ghai-Jain, Iveta Sosova, Alicia Chan, Saadet Mercimek-Andrews
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101055- (2024)
Background: Galactosemia type I is an autosomal recessive disorder of galactose metabolism due to galactose-1-phosphate uridyltransferase deficiency, encoded by GALT. To investigate the phenotypes, genotypes and long-term outcomes of galactosemia, we
Externí odkaz:
https://doaj.org/article/88374486eb8042e7a1ab271fd2577fbb