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Authors :
Jiang Z; a Department of Pathology , Second affiliated hospital of Zhejiang University , Hangzhou , China .; Yu J
Subjects: Mutation*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*chemistry ; Optic Atrophy, Hereditary, Leber/Optic Atrophy, Hereditary, Leber/Optic Atrophy, Hereditary, Leber/*genetics
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Source:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis [Mitochondrial DNA A DNA Mapp Seq Anal] 2016; Vol. 27 (2), pp. 1564-6. Date of Electronic Publication: 2014 Sep 04.Publisher: Taylor & Francis Group Country of Publication: England NLM ID: 101679980 Publication Model: Print-Electronic Cited Medium: Internet ISSN:
تفاصيل العنوان
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Authors :
Ding Y; a Central Laboratory , Hangzhou First People's Hospital , Hangzhou , China .; b Affiliated Hangzhou Hospital, Nanjing Medical University , Hangzhou , China , and.
Subjects: Cardiovascular Diseases/Cardiovascular Diseases/Cardiovascular Diseases/*genetics ; Mitochondria/Mitochondria/Mitochondria/*genetics ; Mutation/Mutation/Mutation/*genetics
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Source:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis [Mitochondrial DNA A DNA Mapp Seq Anal] 2016; Vol. 27 (1), pp. 205-8. Date of Electronic Publication: 2014 Feb 03.Publisher: Taylor & Francis Group Country of Publication: England NLM ID: 101679980 Publication Model: Print-Electronic Cited Medium: Internet ISSN:
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Authors :
Wang X; Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, Illinois, United States of America.; Pan T
Subjects: Genetic Code* ; Mutation* ; Protein Biosynthesis*
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Source:
PLoS genetics [PLoS Genet] 2015 Dec 28; Vol. 11 (12), pp. e1005745. Date of Electronic Publication: 2015 Dec 28 (Print Publication: 2015).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet
تفاصيل العنوان
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Authors :
Zhu Y; Department of Biochemistry, The University of Western Ontario, London, ON N6A 5C1, Canada.; Berg MD
Subjects: Alleles* ; Mutation*; Acetyltransferases/Acetyltransferases/Acetyltransferases/*genetics
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Source:
Biochemistry and cell biology = Biochimie et biologie cellulaire [Biochem Cell Biol] 2020 Oct; Vol. 98 (5), pp. 624-630. Date of Electronic Publication: 2020 May 30.Publisher: Canadian Science Publishing Country of Publication: Canada NLM ID: 8606068 Publication Model: Print-Electronic Cited Medium: Internet
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Authors :
Panecka J; Division of Biophysics, Institute of Experimental Physics, University of Warsaw, Warsaw, Poland; Interdisciplinary Centre for Mathematical and Computational Modelling, University of Warsaw, Warsaw, Poland.
Subjects: Molecular Dynamics Simulation* ; Mutation*; Paromomycin/Paromomycin/Paromomycin/*metabolism
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Source:
PloS one [PLoS One] 2014 Nov 07; Vol. 9 (11), pp. e111811. Date of Electronic Publication: 2014 Nov 07 (Print Publication: 2014).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet
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Authors :
D'Aco KE; Division of Genetics, Department of Pediatrics, University of Rochester School of Medicine and Dentistry, 601 Elmwood Ave, Box 777, Rochester, NY 14623, USA.; Manno M
Subjects: Mutation*; Kidney/Kidney/Kidney/*metabolism ; Kidney Failure, Chronic/Kidney Failure, Chronic/Kidney Failure, Chronic/*genetics
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Source:
Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2013 Mar; Vol. 28 (3), pp. 515-9. Date of Electronic Publication: 2012 Nov 08.Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN:
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Authors :
Tuppen HA; Mitochondrial Research Group, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.; Naess K
Subjects: Mutation*; Deafness/Deafness/Deafness/*genetics ; Epilepsy/Epilepsy/Epilepsy/*genetics
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Source:
European journal of human genetics : EJHG [Eur J Hum Genet] 2012 Aug; Vol. 20 (8), pp. 897-904. Date of Electronic Publication: 2012 Feb 29.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:
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