Literature DB >> 11381601

Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria.

K Tanji1, E Bonilla.   

Abstract

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Year:  2001        PMID： 11381601     DOI： 10.1016/s0091-679x(01)65019-2

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN： 0091-679X            Impact factor:   1.441


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  15 in total

1.  Deletion of mitochondrial anchoring protects dysmyelinating shiverer: implications for progressive MS.

Authors:  Dinesh C Joshi; Chuan-Li Zhang; Tien-Min Lin; Anchal Gusain; Melissa G Harris; Esther Tree; Yewin Yin; Connie Wu; Zu-Hang Sheng; Robert J Dempsey; Zsuzsanna Fabry; Shing Yan Chiu
Journal:  J Neurosci       Date:  2015-04-01       Impact factor: 6.167

2.  Mutation in an mtDNA protein-coding gene: prenatal diagnosis aided by fetal muscle biopsy.

Authors:  Sara Shanske; Ali Naini; Ramen H Chmait; Hasan O Akman; Mahesh Mansukhani; Jiesheng Lu; Michio Hirano; Salvatore DiMauro
Journal:  J Child Neurol       Date:  2012-04-24       Impact factor: 1.987

3.  A history of mitochondrial diseases.

Authors:  Salvatore Dimauro
Journal:  J Inherit Metab Dis       Date:  2010-05-21       Impact factor: 4.982

Review 4.  The clinical maze of mitochondrial neurology.

Authors:  Salvatore DiMauro; Eric A Schon; Valerio Carelli; Michio Hirano
Journal:  Nat Rev Neurol       Date:  2013-07-09       Impact factor: 42.937

5.  Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene.

Authors:  Hasan O Akman; Guido Davidzon; Kurenai Tanji; Emma J Macdermott; Louann Larsen; Mercy M Davidson; Ronald G Haller; Lidia S Szczepaniak; Thomas J A Lehman; Michio Hirano; Salvatore DiMauro
Journal:  Neuromuscul Disord       Date:  2010-05-14       Impact factor: 4.296

6.  The hidden cost of sexually selected traits: the metabolic expense of maintaining a sexually selected weapon.

Authors:  Ummat Somjee; H Arthur Woods; Meghan Duell; Christine W Miller
Journal:  Proc Biol Sci       Date:  2018-11-14       Impact factor: 5.349

7.  Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) gene.

Authors:  Jorida Coku; Sara Shanske; Mahsa Mehrazin; Kurenai Tanji; Ali Naini; Valentina Emmanuele; Marc Patterson; Michio Hirano; Salvatore DiMauro
Journal:  J Neurol Sci       Date:  2009-12-22       Impact factor: 3.181

8.  Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM gene.

Authors:  Lorenzo Peverelli; Carl A Gold; Ali B Naini; Kurenai Tanji; H Orhan Akman; Michio Hirano; Salvatore Dimauro
Journal:  Muscle Nerve       Date:  2014-08       Impact factor: 3.217

Review 9.  Long survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature.

Authors:  Rebecca J Levy; Purificación Gutierrez Ríos; Hasan O Akman; Monica Sciacco; Darryl C De Vivo; Salvatore DiMauro
Journal:  J Child Neurol       Date:  2013-11-27       Impact factor: 1.987

Review 10.  Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations.

Authors:  Carlos T Moraes; David P Atencio; Jose Oca-Cossio; Francisca Diaz
Journal:  J Mol Diagn       Date:  2003-11       Impact factor: 5.568
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