Zobrazeno 1 - 10
of 25
pro vyhledávání: '"VLCFA, very long chain fatty acids"'
Autor:
Marguerite Batsale, Marie Alonso, Stéphanie Pascal, Didier Thoraval, Richard P. Haslam, Frédéric Beaudoin, Frédéric Domergue, Jérôme Joubès
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
Very-long-chain fatty acids (VLCFA) are precursors for various lipids playing important physiological and structural roles in plants. Throughout plant tissues, VLCFA are present in multiple lipid classes essential for membrane homeostasis, and also s
Externí odkaz:
https://doaj.org/article/8638f9feb93143f7a393e8585396381f
Akademický článek
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Autor:
A. Paisiou, M. Rogalidou, R. Pons, E. Ioannidou, K. Dimakou, A. Papadopoulou, F.M. Vaz, G. Vessalas, S.M.I. Goorden, J. Roelofsen, A. Zoetekouw, M.M. Nieman, E. Dimitriou, M. Moraitou, I. Peristeri, H. Michelakakis, A.B.P. van Kuilenburg
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 30, Iss, Pp 100829-(2022)
Molecular Genetics and Metabolism Reports, Vol 30, Iss, Pp 100829-(2022)
We describe the case of a Greek female patient with the Classic form of the ultra- rare and fatal autosomal recessive disorder Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) and the impact of allogeneic hematopoietic stem cell transpla
Autor:
Hafiz, Muhammad Ahmad, Xiukang, Wang, Sajid, Fiaz, Mahmood-Ur-Rahman, Muhammad, Azhar Nadeem, Sher, Aslam Khan, Sunny, Ahmar, Farrukh, Azeem, Tayyaba, Shaheen, Freddy, Mora-Poblete
Publikováno v:
Saudi Journal of Biological Sciences
Sunflower occupies the fourth position among oilseed crops the around the world. Eceriferum (CER) is an important gene family that plays critical role in very-long-chain fatty acids elongation and biosynthesis of epicuticular waxes under both biotic
Autor:
Natalia A, Semenova, Marina V, Kurkina, Andrey V, Marakhonov, Elena L, Dadali, Natalia N, Taran, Tatyana V, Strokova
Publikováno v:
Molecular Genetics and Metabolism Reports
Background Peroxisome biogenesis disorders (PBD) are a heterogeneous group of autosomal recessive disorders that affect multiple organ systems. Approximately 80% of PBD patients are classifiedin the Zellweger syndrome spectrum, which is generally cau
Autor:
Susan Walker, Whiwon Lee, Hernan Gonorazky, Gregory Costain, Susan Blaser, Christian R. Marshall, Michal Inbar-Feigenberg
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100664-(2020)
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100664-(2020)
Defects in PEX3 are associated with a severe neonatal-lethal form of Zellweger spectrum disorder. We report two moderately affected siblings whose clinical and biochemical phenotypes expand the reported spectrum of PEX3-related disease. Genome sequen
Autor:
Aqeela H. Alhashim, Dalya S. Alam, Abdulaziz N. AlSaad, Riyam F. AlAnazi, Mohammed H. AlBanji, Zahra A. Aleisa
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100665-(2020)
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100665-(2020)
Introduction Hypotonia is a common presentation that child neurologists encounter daily. The hypotonic neonate represents a diagnostic challenge as a lesion at any level in the neuro-axis may cause hypotonia. In this paper, we study the diagnostic yi
Publikováno v:
Biochimie
Currently the molecular basis for the clinical heterogeneity of X-linked adrenoleukodystrophy (X-ALD) is poorly understood. The genetic bases for all different phenotypic variants of X-ALD are mutations in the gene encoding the peroxisomal ATP-bindin
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Akademický článek
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