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Akademický článek

The minimal SUF system is not required for Fe–S cluster biogenesis in the methanogenic archaeon Methanosarcina acetivorans

Autor: Jasleen Saini, Thomas M. Deere, Daniel J. Lessner

Publikováno v: Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)

Abstract Iron–sulfur (Fe–S) proteins are essential for the ability of methanogens to carry out methanogenesis and biological nitrogen fixation (diazotrophy). Nonetheless, the factors involved in Fe–S cluster biogenesis in methanogens remain lar

Externí odkaz: https://doaj.org/article/915b17eb545243b280e3d5a98ea4e891

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Akademický článek

Methanosarcina acetivorans contains a functional ISC system for iron-sulfur cluster biogenesis

Autor: Thomas M. Deere, Divya Prakash, Faith H. Lessner, Evert C. Duin, Daniel J. Lessner

Publikováno v: BMC Microbiology, Vol 20, Iss 1, Pp 1-16 (2020)

Abstract Background The production of methane by methanogens is dependent on numerous iron-sulfur (Fe-S) cluster proteins; yet, the machinery involved in Fe-S cluster biogenesis in methanogens remains largely unknown. Methanogen genomes encode unchar

Externí odkaz: https://doaj.org/article/ccedc92bd4584154975087fbd8309cd7

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Methanosarcina acetivorans

Autor: Jasleen Saini, Thomas M. Deere, Melissa Chanderban, Gary J. McIntosh, Daniel J. Lessner

Publikováno v: Trends in Microbiology. 31:320-321

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ebfb734e7f94e6ed12a0a7d1607f358
https://doi.org/10.1016/j.tim.2022.10.001

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Vht hydrogenase is required for hydrogen cycling during nitrogen fixation by the non-hydrogenotrophic methanogen Methanosarcina acetivorans

Autor: Thomas M. Deere, Daniel J. Lessner, Jadelyn M. Hoerr, Ahmed E. Dhamad, Melissa Chanderban

Methanosarcina acetivorans is the primary model to understand the physiology of methanogens that do not use hydrogenase to consume or produce hydrogen (H2) during methanogenesis. The genome of M. acetivorans encodes putative methanophenazine-reducing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2e6c269f14dd8c9ca509b116cd658d1b
https://doi.org/10.1101/2021.10.12.464174

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Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia

Autor: M, Deere, T, Sanford, C A, Francomano, K, Daniels, J T, Hecht

Publikováno v: American journal of medical genetics. 85(5)

Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (EDM1) are allelic disorders caused by mutations in the gene encoding cartilage oligomeric matrix protein (COMP). PSACH is a dominant condition characterized by disproportionate short sta

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1b928ed7c7df4a5b251d3493d0466eb3
https://pubmed.ncbi.nlm.nih.gov/10405447

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Genomic characterization of human DSPG3

Autor: M, Deere, J L, Dieguez, S J, Yoon, D, Hewett-Emmett, A, de la Chapelle, J T, Hecht

Publikováno v: Genome research. 9(5)

DSPG3, the human homolog to chick PG-Lb, is a member of the small leucine-rich repeat proteoglycan (SLRP) family, including decorin, biglycan, fibromodulin, and lumican. In contrast to the tissue distribution of the other SLRPs, DSPG3 is predominantl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a5d01e2291d09c329806a7990c6c37f7
https://pubmed.ncbi.nlm.nih.gov/10330124

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Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia

Autor: M, Deere, T, Sanford, H L, Ferguson, K, Daniels, J T, Hecht

Publikováno v: American journal of medical genetics. 80(5)

Pseudoachondroplasia (PSACH) is an autosomal dominant dwarfing condition characterized by disproportionate short stature, joint laxity, and early-onset osteoarthrosis. PSACH is caused by mutations in the gene encoding cartilage oligomeric matrix prot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc59f2e1bfe5243d1488ddcbc304da9d
https://pubmed.ncbi.nlm.nih.gov/9880218

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Mosaicism in pseudoachondroplasia

Autor: H L, Ferguson, M, Deere, R, Evans, J, Rotta, J G, Hall, J T, Hecht

Publikováno v: American journal of medical genetics. 70(3)

Pseudoachondroplasia (PSACH) is a spondylo-epi-metaphyseal dysplasia characterized by disproportionate short stature, generalized ligamentous laxity, and precocious osteoarthritis. PSACH is caused by mutations in the cartilage oligomeric matrix prote

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9327c7fe81839878aa414733657b7109
https://pubmed.ncbi.nlm.nih.gov/9188668

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Genetic heterogeneity in multiple epiphyseal dysplasia

Autor: M, Deere, S H, Blanton, C I, Scott, L O, Langer, R M, Pauli, J T, Hecht

Publikováno v: American journal of human genetics. 56(3)

Multiple epiphyseal dysplasia (MED) comprises a group of hereditary chondrodysplasias in which there are major anatomic abnormalities of the long tubular bones. The Fairbank and Ribbing types are the most frequently cited types of MED. They are prima

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b32f44cc3c5b4a8172d4a583fc0e0272
https://pubmed.ncbi.nlm.nih.gov/7887425

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Akademický článek

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