₈Michael T Ryan

Summary for 2004 [at-glance overview of Michael T Ryan work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Michael T Ryan. According to available data, in 2004 Michael T Ryan published at least 8 articles. This work was completed in collaboration with several authors including Thorburn, David R and Kirby, Denise M. Many other authors have collaborated with Michael T Ryan as well. At least 6 different grants are awarded to Michael T Ryan to support this work. All time total of the grant awards on file exceeds $974,567.

Michael T Ryan has rank 89 when compared to all other authors using the keyword DNA, Mitochondrial. Analysis of the article abstracts and the titles suggests that Michael T Ryan professional interests are focused around "mitochondrial outer membrane", "respiratory chain disorders" and "using blue native". These might also be referred to as "complex deficiency", "respiratory chain" or "infantile mitochondrial". Statistical analysis shows that Michael T Ryan's writing is likely to contains terms "mitochondrial", "complex", "presenilin", "mutations", "patients" and "gene".

Unfortunately, there is not enough information to establish Michael T Ryan affiliation. Luckily, several email addresses are on file.

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Alternative names (1) [other authors with names similar to Michael T Ryan]

₁₈Ryan, M T

Year 2004 Charts [Michael T Ryan frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Michael T Ryan publication and funding history for the range of years]

Emails (3) [email addresses extracted from Michael T Ryan affiliations]

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Michael T Ryan Coauthors (22) [all coauthors with the number of joint publications]

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₁₄Turnbull, Douglass M

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₂Williamson, Nicholas A

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Affiliations (6) [condensed summary of the Michael T Ryan affiliations, the leading number and the color conveys importance]

₂Murdoch Children's Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria 3052 Australia.
₂Department of Biochemistry, La Trobe University, 3086 3088, Melbourne, Australia.
₁Charleston Southern University, Charleston, SC 29423-8087, USA.
₁Dade W. Moeller & Associates Inc., 257 River Island Road, New Bern, NC 28562, USA.
₁Department of Pathology, The University of Melbourne, Australia.
₁Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, University of Newcastle upon Tyne, United Kingdom.

Key Opinion Leader In [Michael T Ryan is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

₈₉DNA, Mitochondrial

Keywords (32) [keywords assigned to Michael T Ryan articles by PubMed, the leading number and the color conveys importance]

₇Humans | ₄Female | ₃DNA, Mitochondrial | ₃Male | ₃Mutation | ₂Electron Transport Complex I | ₂Models, Biological | ₂Genetic Complementation Test | ₂Animals | ₂Mitochondria | ₂Adult | ₁Base Sequence | ₁Intracellular Membranes | ₁Infant, Newborn | ₁Brain | ₁Adolescent | ₁Cytoskeletal Proteins | ₁Body Burden | ₁Recombinant Fusion Proteins | ₁Hela Cells | ₁Sequence Homology, Amino Acid | ₁Sequence Deletion | ₁Membrane Glycoproteins | ₁Protein Structure, Tertiary | ₁Diet | ₁Radiation Dosage | ₁Amyloid Precursor Protein Secretases | ₁Cell Fusion | ₁Health Physics | ₁Mitochondrial Diseases | ₁Exons | ₁Radioactive Waste

Michael T Ryan Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Michael T Ryan might be a good expert witness on these terms]

₃₄mitochondrial | ₂₅complex | ₁₉presenilin | ₁₉mutations | ₁₀patients | ₉gene | ₉mutation | ₈deficiency | ₈chain | ₈respiratory | ₈brain | ₈cause | ₇disease | ₇genes | ₇disorders | ₇water | ₇membrane | ₆129i | ₆infantile | ₆outer | ₆human | ₆analysis | ₅dna | ₅proteins | ₅nd3 | ₅using | ₅membranes | ₅expression | ₄ground | ₄mtdna | ₄cells | ₄mouse
₈complex deficiency | ₈respiratory chain | ₆infantile mitochondrial | ₆outer membrane | ₅mitochondrial dna | ₅mitochondrial outer | ₅presenilin complex | ₄ground water | ₄mitochondrial morphology | ₄chain disorders | ₄de novo | ₄upper bound | ₃gel electrophoresis | ₃using blue | ₃blue native | ₃mitochondrial encephalopathies | ₃complex mobility | ₃native gel | ₃novo mutations | ₃mouse human | ₃cause infantile | ₃pharynx defective-1 | ₃human brain | ₃human fis1 | ₃presenilin enhancer-2 | ₃nicastrin presenilin | ₃anterior pharynx | ₃embryonic brain | ₂annual committed | ₂chain subunits | ₂encephalopathy complex | ₂neonatal mitochondrial
₅mitochondrial outer membrane | ₄respiratory chain disorders | ₃using blue native | ₃blue native gel | ₃infantile mitochondrial encephalopathies | ₃native gel electrophoresis | ₃nicastrin presenilin enhancer-2 | ₃anterior pharynx defective-1 | ₃cause infantile mitochondrial | ₃de novo mutations | ₃mouse human brain | ₂novel cause lethal | ₂characterization presenilin complexes | ₂human brain using | ₂infantile mitochondrial encephalopathy | ₂mitochondrial complex deficiency | ₂pathogenic presenilin mutations | ₂regulate mitochondrial morphology | ₂mitochondrial dna mutations | ₂brain using blue | ₂electrophoresis reveals expression | ₂minimal change complex | ₂beta barrels membranes | ₂levels human fis1 | ₂ndufs6 mutations novel | ₂reveals expression embryonic | ₂nd3 gene cause | ₂mutations novel cause | ₂gene cause infantile | ₂gel electrophoresis reveals | ₂association nicastrin presenilin | ₂upper bound annual

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