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pro vyhledávání: '"1301 Biochemistry, Genetics and Molecular Biology (miscellaneous)"'
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Diploid plant genomes typically contain ~35,000 genes, almost all belonging to highly conserved gene families. Only a small fraction are lineage-specific, which are found in only one or few closely related species. Little is known about
Diploid plant genomes typically contain ~35,000 genes, almost all belonging to highly conserved gene families. Only a small fraction are lineage-specific, which are found in only one or few closely related species. Little is known about
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757b5db29180f05101cc61df9265aa2c
https://doi.org/10.5167/uzh-233953
https://doi.org/10.5167/uzh-233953
Autor:
Beat Thöny, Zumira Aparecida Carneiro, Marcela Almeida, Isabela F. Lopes, Laura Vagnini, Laís C. Silva, Jacqueline Fonseca, Charles Marques Lourenço, Janaina Dovidio
Publikováno v:
JIMD Reports
JIMD Reports, Vol 61, Iss 1, Pp 19-24 (2021)
JIMD Reports, Vol 61, Iss 1, Pp 19-24 (2021)
Tetrahydrobiopterin (BH4) is a cofactor that participates in the biogenesis reactions of a variety of biomolecules, including l‐tyrosine, l‐3,4‐dihydroxyphenylalanine, 5‐hydroxytryptophan, nitric oxide, and glycerol. Dihydropteridine reductas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f9e3255be6f53f36392b9f4849fe8ae
https://doi.org/10.1002/jmd2.12224
https://doi.org/10.1002/jmd2.12224
Autor:
Li Zhang, Felicia Dietsche, Bruno Seitaj, Liliana Rojas-Charry, Nadina Latchman, Dhanendra Tomar, Rob CI Wüst, Alexander Nickel, Katrin BM Frauenknecht, Benedikt Schoser, Sven Schumann, Michael J Schmeisser, Johannes vom Berg, Thorsten Buch, Stefanie Finger, Philip Wenzel, Christoph Maack, John W Elrod, Jan B Parys, Geert Bultynck, Axel Methner
Publikováno v:
Life science alliance, 5(10):e202201478, 1-15. Rockefeller University Press
Zhang, L, Dietsche, F, Seitaj, B, Rojas-Charry, L, Latchman, N, Tomar, D, Wüst, R C, Nickel, A, Frauenknecht, K B, Schoser, B, Schumann, S, Schmeisser, M J, Vom Berg, J, Buch, T, Finger, S, Wenzel, P, Maack, C, Elrod, J W, Parys, J B, Bultynck, G & Methner, A 2022, ' TMBIM5 loss of function alters mitochondrial matrix ion homeostasis and causes a skeletal myopathy ', Life science alliance, vol. 5, no. 10, e202201478, pp. 1-15 . https://doi.org/10.26508/lsa.202201478
Zhang, L, Dietsche, F, Seitaj, B, Rojas-Charry, L, Latchman, N, Tomar, D, Wüst, R C, Nickel, A, Frauenknecht, K B, Schoser, B, Schumann, S, Schmeisser, M J, Vom Berg, J, Buch, T, Finger, S, Wenzel, P, Maack, C, Elrod, J W, Parys, J B, Bultynck, G & Methner, A 2022, ' TMBIM5 loss of function alters mitochondrial matrix ion homeostasis and causes a skeletal myopathy ', Life science alliance, vol. 5, no. 10, e202201478, pp. 1-15 . https://doi.org/10.26508/lsa.202201478
Ion fluxes across the inner mitochondrial membrane control mitochondrial volume, energy production, and apoptosis. TMBIM5, a highly conserved protein with homology to putative pH-dependent ion channels, is involved in the maintenance of mitochondrial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c011d27b2946bcb5b6358afd11e5522
https://pubmed.ncbi.nlm.nih.gov/35715207
https://pubmed.ncbi.nlm.nih.gov/35715207
Publikováno v:
Cell Stress, Vol 4, Iss 6, Pp 147-150 (2020)
Dysregulation of the mitochondrial network in terminally differentiated cells contributes to a broad spectrum of disorders. Methylmalonic acidemia (MMA) is an autosomal recessive inborn error of intermediary metabolism caused by the deficiency of met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0f385e4e669bfad90879dc1985f687a
https://doi.org/10.15698/cst2020.06.222
https://doi.org/10.15698/cst2020.06.222
Publikováno v:
JIMD Reports, Vol 53, Iss 1, Pp 12-15 (2020)
JIMD Reports
JIMD Reports
Tyrosine hydroxylase deficiency is a rare autosomal recessive, treatable disorder of neurotransmission. Fewer than 100 cases have been reported so far. We present a case of a 10‐month‐old infant who was symptomatic since 5 months of age and who r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea2e788ff4281030c13a2df55ea4a3c
https://doi.org/10.1002/jmd2.12111
https://doi.org/10.1002/jmd2.12111
Autor:
Chen, Zhenyue, Zhou, Quanyu, Deán‐Ben, Xosé Luís, Gezginer, Irmak, Ni, Ruiqing, Reiss, Michael, Shoham, Shy, Razansky, Daniel
Publikováno v:
Advanced Science, 9 (24)
Modern optical neuroimaging approaches are expanding the ability to elucidate complex brain function. Diverse imaging contrasts enable direct observation of neural activity with functional sensors along with the induced hemodynamic responses. To date
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a84af8cba072297596a33f5912069dd
Autor:
Tobias Hasler, Leticia Tavares-Gomes, Sereina Gut, Meghna Swayambhu, Mario Gysi, Martin Hausmann, Natasha Arora, Thierry Hennet
The availability of endogenous and dietary carbohydrates in the gastrointestinal tract influences the composition of the gut microbiota. Carbohydrate foraging requires the action of bacterially-encoded glycoside hydrolases, which release mono- and ol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98b19e632b13b8e23e3da06fa6cc1a77
https://www.zora.uzh.ch/id/eprint/226421/
https://www.zora.uzh.ch/id/eprint/226421/
Publikováno v:
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences, Vol 8 (2021)
Frontiers in Molecular Biosciences, Vol 8 (2021)
Alternative splicing is an essential regulatory mechanism for gene expression in mammalian cells contributing to protein, cellular, and species diversity. In cancer, alternative splicing is frequently disturbed, leading to changes in the expression o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95cef150a2474a4a502c505272cbeed8
https://doi.org/10.3389/fmolb.2021.726902
https://doi.org/10.3389/fmolb.2021.726902