About: Michael T Ryan

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Australian mitochondrial biologist

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) Australian mitochondrial biologist (en)
rdfs:label	Michael T Ryan (en) Michael T Ryan (es) Michael T Ryan (nl) Michael T Ryan (sl) Michael T Ryan (ast) Michael T. Ryan (it) মাইকেল টি রায়ান (bn)
skos:prefLabel	Michael T Ryan (en) Michael T Ryan (es) Michael T Ryan (nl) Michael T Ryan (sl) Michael T Ryan (ast) Michael T. Ryan (it) মাইকেল টি রায়ান (bn)
name	Michael T Ryan (en) Michael T Ryan (es) Michael T Ryan (nl) Michael T Ryan (sl) Michael T Ryan (ast) Michael T. Ryan (it) মাইকেল টি রায়ান (bn)
LinkedIn personal profile ID	wds:Q37381043-83d257e8-4412-26b6-82a9-2eb1660cb7a6
LinkedIn personal profile ID	mike-ryan-00b928126
given name	wds:Q37381043-3E37DC50-55CE-4C76-8A50-0FF6B94D0E8E
given name	Michael
instance of	wds:Q37381043-1AAD440D-FB1F-4928-893B-3E3F0DD2575B
instance of	Homo sapiens
award received	wds:Q37381043-93bc9ecc-4f61-b1f3-2c6b-02d474bbcbf4
award received	Lemberg Medal
Google Scholar author ID	wds:Q37381043-5df64d2f-40ab-47e9-3deb-c2bfca4d8342
Google Scholar author ID	LPydMdEAAAAJ
skos:altLabel	Mike Ryan (en) Michael Ryan (en)
occupation	wds:Q37381043-83f08042-4d27-1cca-53b8-3976c71c3e20 wds:Q37381043-D8B66C8F-7ED7-4179-8937-F4942F2CAAA1
employer	wds:Q37381043-924B932A-39A9-4A23-9985-2261497C3EE8 wds:Q37381043-C63FB8AC-A60E-4701-8131-3E41065649C7
NLA Trove people ID	wds:Q37381043-ECDA328C-7231-459C-AA05-80101640BEB2
sex or gender	wds:Q37381043-A58C015D-7229-47B2-98B5-AE357781ACFF
family name	wds:Q37381043-02EFBCEF-B770-42EB-82FA-6419C1C59294
occupation	researcher biologist
employer	Monash University La Trobe University
NLA Trove people ID	1599879
sex or gender	male
family name	Ryan
Springer Nature person ID	wds:Q37381043-83C58189-E490-4276-95B3-556914154AA7
ORCID iD	wds:Q37381043-F5C78209-1EEC-4AF5-806F-B0185EFBC529
Dimensions author ID	wds:Q37381043-1F978799-B138-42BE-9611-04BB65FAB90C
ORCID iD	https://orcid.org/0000-0003-2586-8829
Springer Nature person ID	0721644642.91
ORCID iD	0000-0003-2586-8829
Dimensions author ID	0721644642.91
ResearcherID	wds:Q37381043-DCDC209A-F879-43CA-97BF-CF519088AB5D
Publons author ID	wds:Q37381043-5b7ddfc5-0413-4348-9a96-77542b34e194
ResearcherID	C-6673-2011
Publons author ID	2800904
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37381043
is author of	MiD49 and MiD51, new components of the mitochondrial fission machinery Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients Accessory subunits are integral for assembly and function of human mitochondrial complex I. Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I Assembly of mitochondrial complex I and defects in disease Splitting up the powerhouse: structural insights into the mechanism of mitochondrial fission De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex. Essential role of Isd11 in mitochondrial iron-sulfur cluster synthesis on Isu scaffold proteins The regulation of mitochondrial morphology: intricate mechanisms and dynamic machinery Machinery for protein sorting and assembly in the mitochondrial outer membrane Biochemical and molecular diagnosis of mitochondrial respiratory chain disorders. Analysis of mitochondrial subunit assembly into respiratory chain complexes using Blue Native polyacrylamide gel electrophoresis. Structural and functional analysis of MiD51, a dynamin receptor required for mitochondrial fission FunRich: An open access standalone functional enrichment and interaction network analysis tool Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1 Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I Assembly factors of human mitochondrial complex I and their defects in disease Understanding mitochondrial complex I assembly in health and disease Next-generation sequencing in molecular diagnosis:NUBPLmutations highlight the challenges of variant detection and interpretation Impaired Folding of the Mitochondrial Small TIM Chaperones Induces Clearance by the i-AAA Protease Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype Mitochondrial protein import machineries and lipids: a functional connection

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