Zobrazeno 1 - 10
of 157
pro vyhledávání: '"Molybdenum cofactor sulfurase"'
Autor:
Nicole M. Tate, Katie M. Minor, Jody P. Lulich, James R. Mickelson, Allyson Berent, Jonathan D. Foster, Kasey H. Petersen, Eva Furrow
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100792- (2021)
Hereditary xanthinuria is a rare autosomal recessive disease caused by missense and loss of function variants in the xanthine dehydrogenase (XDH) or molybdenum cofactor sulfurase (MOCOS) genes. The aim of this study was to uncover variants underlying
Externí odkaz:
https://doaj.org/article/d0d68e09b2a84a188ca82aec80814820
Autor:
Amin Safa, Mir Davood Omrani, Fwad Nicknafs, Alireza Komaki, Mohammad Taheri, Soudeh Ghafouri-Fard
Publikováno v:
Frontiers in Molecular Biosciences, Vol 7 (2020)
BackgroundMolybdenum cofactor sulfurase (MOCOS) is an enzyme participating in purine metabolism. The aim of current study was to evaluate the role of a single nucleotide polymorphism (SNP) in the coding gene (rs594445) in mood disorders and methamphe
Externí odkaz:
https://doaj.org/article/470ae769256b4e1aa5b9cbb71c66d530
Akademický článek
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Autor:
Yunan Zhou, Xueguang Zhang, Rui Ding, Zuoxiang Li, Quan Hong, Yan Wang, Wei Zheng, Xiaodong Geng, Meng Fan, Guangyan Cai, Xiangmei Chen, Di Wu
Publikováno v:
Cellular Physiology and Biochemistry, Vol 35, Iss 6, Pp 2412-2421 (2015)
Background: Hypouricemia is caused by various diseases and disorders, such as hepatic failure, Fanconi renotubular syndrome, nutritional deficiencies and genetic defects. Genetic defects of the molybdoflavoprotein enzymes induce hypouricemia and xant
Externí odkaz:
https://doaj.org/article/a8e4e801589c4ae5a92a16643fc48ce4
Autor:
Nicole M, Tate, Katie M, Minor, Jody P, Lulich, James R, Mickelson, Allyson, Berent, Jonathan D, Foster, Kasey H, Petersen, Eva, Furrow
Publikováno v:
Molecular Genetics and Metabolism Reports
Hereditary xanthinuria is a rare autosomal recessive disease caused by missense and loss of function variants in the xanthine dehydrogenase (XDH) or molybdenum cofactor sulfurase (MOCOS) genes. The aim of this study was to uncover variants underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46700f034c9f08a1896a11a2aeaaf926
https://pubmed.ncbi.nlm.nih.gov/34584846
https://pubmed.ncbi.nlm.nih.gov/34584846
Publikováno v:
Clinica Chimica Acta. 504:168-171
Xanthinuria is a rare genetic metabolic disorder, the biochemical mechanism of xanthinuria is the disturbance of purine to uric acid metabolism due to the deficiency of xanthine dehydrogenase/xanthine oxidase (XDH/XO) and aldehyde oxidase 1 (AOX1). X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f259949b54b8756588e799451f2d7b97
https://doi.org/10.1016/j.cca.2020.02.012
https://doi.org/10.1016/j.cca.2020.02.012
Autor:
Madeleine Erard-Garcia, Sylvie Mavel, Ana Dudas, Michael J. Mihatsch, Julie Pailloux, Claire Mackowiak, Frédéric Foucher, Pauline Rontani, Nicolas Erard, Elodie Culerier, Bernhard Ryffel, Marc Le Bert, Valérie F. J. Quesniaux, Delphine Sedda, Antoine Lefevre, Patrick Emond
Publikováno v:
Kidney360
Kidney360, 2021, pp.10.34067/KID.0001732021. ⟨10.34067/kid.0001732021⟩
Kidney360, 2021, pp.10.34067/KID.0001732021. ⟨10.34067/kid.0001732021⟩
Background Xanthinuria type II is a rare autosomal purine disorder. This recessive defect of purine metabolism remains an under-recognized disorder. Methods Mice with targeted disruption of the molybdenum cofactor sulfurase (Mocos) gene were generate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a958596497f8a263cf84344fc6abc3b8
https://hal.archives-ouvertes.fr/hal-03429645
https://hal.archives-ouvertes.fr/hal-03429645
Autor:
Philippa M. Gibbons, Eva Furrow, Raquel R. Rech, Tasha Likavec, Krystal J Vail, Katie M. Minor, Nicole M. Tate
Publikováno v:
Journal of Veterinary Internal Medicine
A 2‐year‐old mixed breed goat was presented for a 1‐day history of anorexia and 1 week of weight loss. Serum biochemistry disclosed severe azotemia. Abdominal ultrasound examination showed decreased renal corticomedullary distinction, poor visu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::596e29b921388c633687e1e93af2d59f
https://doi.org/10.1111/jvim.15431
https://doi.org/10.1111/jvim.15431
Autor:
Paiboon Tunsagool, Janthima Jaresitthikunchai, Sittiruk Roytrakul, Warangkana Jutidamrongphan, Narumon Phaonakrop, Wichitra Leelasuphakul
Publikováno v:
Plant Cell Reports. 38:559-575
Bacillus subtilis CLP extract activates defense gene expression and increases the unique protein production involving in pathways of ISR, SAR, ubiquitin-proteasome system, and glycolysis for stress responses in flavedo tissues. Cyclic lipopeptides (C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea37268ba3f3b4fb7b4cb5316e9c060
https://doi.org/10.1007/s00299-019-02386-1
https://doi.org/10.1007/s00299-019-02386-1
Publikováno v:
Animal geneticsReferences. 52(4)
Qira black sheep is a famous indigenous sheep breed in China. The objectives of this study are to identify candidate genes related to body size, and to estimate the level of inbreeding depression on body size based on runs of homozygosity in Qira bla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04b10e258bf64d7af97a6aba15488733
https://pubmed.ncbi.nlm.nih.gov/34096079
https://pubmed.ncbi.nlm.nih.gov/34096079