Literature DB >> 10051550

Mitochondria and dystonia: the movement disorder connection?

D C Wallace1, D G Murdock.   

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Year:  1999        PMID: 10051550      PMCID: PMC33525          DOI: 10.1073/pnas.96.5.1817

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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  26 in total

1.  A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.

Authors:  B H Graham; K G Waymire; B Cottrell; I A Trounce; G R MacGregor; D C Wallace
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

2.  Import of mitochondrial carriers mediated by essential proteins of the intermembrane space.

Authors:  C M Koehler; E Jarosch; K Tokatlidis; K Schmid; R J Schweyen; G Schatz
Journal:  Science       Date:  1998-01-16       Impact factor: 47.728

3.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

4.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

5.  Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Authors:  A S Jun; I A Trounce; M D Brown; J M Shoffner; D C Wallace
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

6.  Human deafness dystonia syndrome is a mitochondrial disease.

Authors:  C M Koehler; D Leuenberger; S Merchant; A Renold; T Junne; G Schatz
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

7.  The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.

Authors:  L J Ozelius; J W Hewett; C E Page; S B Bressman; P L Kramer; C Shalish; D de Leon; M F Brin; D Raymond; D P Corey; S Fahn; N J Risch; A J Buckler; J F Gusella; X O Breakefield
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

8.  A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness.

Authors:  H Jin; M May; L Tranebjaerg; E Kendall; G Fontán; J Jackson; S H Subramony; F Arena; H Lubs; S Smith; R Stevenson; C Schwartz; D Vetrie
Journal:  Nat Genet       Date:  1996-10       Impact factor: 38.330

9.  Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.

Authors:  T Bourgeron; P Rustin; D Chretien; M Birch-Machin; M Bourgeois; E Viegas-Péquignot; A Munnich; A Rötig
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

10.  Leber's disease and dystonia: a mitochondrial disease.

Authors:  E J Novotny; G Singh; D C Wallace; L J Dorfman; A Louis; R L Sogg; L Steinman
Journal:  Neurology       Date:  1986-08       Impact factor: 9.910

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  12 in total

1.  Previously uncharacterized genes in the UV- and MMS-induced DNA damage response in yeast.

Authors:  Denise Hanway; Jodie K Chin; Gang Xia; Guy Oshiro; Elizabeth A Winzeler; Floyd E Romesberg
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

2.  Neuroprotective and neurorestorative strategies for neuronal injury.

Authors:  M F Beal; T Palomo; R M Kostrzewa; T Archer
Journal:  Neurotox Res       Date:  2000       Impact factor: 3.911

3.  Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Authors:  Sarah Doss; Katja Lohmann; Philip Seibler; Björn Arns; Thomas Klopstock; Christine Zühlke; Karen Freimann; Susen Winkler; Thora Lohnau; Mario Drungowski; Peter Nürnberg; Karin Wiegers; Ebba Lohmann; Sadaf Naz; Meike Kasten; Georg Bohner; Alfredo Ramirez; Matthias Endres; Christine Klein
Journal:  J Neurol       Date:  2013-11-08       Impact factor: 4.849

4.  Mitochondrial DNA as a cancer biomarker.

Authors:  John P Jakupciak; Wendy Wang; Maura E Markowitz; Delphine Ally; Michael Coble; Sudhir Srivastava; Anirban Maitra; Peter E Barker; David Sidransky; Catherine D O'Connell
Journal:  J Mol Diagn       Date:  2005-05       Impact factor: 5.568

5.  Thiamine and dystonia 16.

Authors:  Antonio Costantini; Erika Trevi; Maria Immacolata Pala; Roberto Fancellu
Journal:  BMJ Case Rep       Date:  2016-07-22

6.  Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes.

Authors:  Anna Sedivá; C I Edvard Smith; A Charlotta Asplund; Jan Hadac; Ales Janda; Jirí Zeman; Hana Hansíková; Lenka Dvoráková; Lenka Mrázová; Sirje Velbri; Carla Koehler; Karin Roesch; Kathleen E Sullivan; Takeshi Futatani; Hans D Ochs
Journal:  J Clin Immunol       Date:  2007-09-12       Impact factor: 8.317

Review 7.  The focal dystonias: current views and challenges for future research.

Authors:  H A Jinnah; Alfredo Berardelli; Cynthia Comella; Giovanni Defazio; Mahlon R Delong; Stewart Factor; Wendy R Galpern; Mark Hallett; Christy L Ludlow; Joel S Perlmutter; Ami R Rosen
Journal:  Mov Disord       Date:  2013-06-15       Impact factor: 10.338

8.  An exploratory analysis of mitochondrial haplotypes and allogeneic hematopoietic cell transplantation outcomes.

Authors:  Julie A Ross; Jakub Tolar; Logan G Spector; Todd DeFor; Troy C Lund; Daniel J Weisdorf; Erica Langer; Anthony J Hooten; Bharat Thyagarajan; Michelle K Gleason; John E Wagner; Kimberly Robien; Michael R Verneris
Journal:  Biol Blood Marrow Transplant       Date:  2014-10-06       Impact factor: 5.742

9.  The Mitochondrial Endonuclease M20 Participates in the Down-Regulation of Mitochondrial DNA in Pollen Cells.

Authors:  Fei Ma; Hui Qi; Yu-Fei Hu; Qian-Ru Jiang; Li-Guang Zhang; Peng Xue; Fu-Quan Yang; Rui Wang; Yan Ju; Hidenobu Uchida; Quan Zhang
Journal:  Plant Physiol       Date:  2018-10-09       Impact factor: 8.340

10.  A case of mitochondrial cytopathy with exertion induced dystonia.

Authors:  Sadanandavalli Retnaswami Chandra; Thomas Gregor Issac
Journal:  J Pediatr Neurosci       Date:  2015 Jul-Sep
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