✦ LIBER ✦

A Mutation in Mitochondrial Complex I Increases Ethanol Sensitivity in Caenorhabditis elegans

✍ Scribed by Ernst-Bernhard Kayser; Charles L. Hoppel; Phil G. Morgan; Margaret M. Sedensky

Book ID: 109123311
Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 565 KB
Volume: 27
Category: Article
ISSN: 0145-6008
DOI: 10.1111/j.1530-0277.2003.tb04394.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation in a mitochondrial ribosomal pr

Mutation in a mitochondrial ribosomal protein causes increased sensitivity to oxygen with decreased longevity in the nematode Caenorhabditis elegans

✍ Michihiko Fujii; Kazuki Shikatani; Ken-Ichi Ogura; Yoshio Goshima; Dai Ayusawa 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 628 KB

A mutation in Caenorhabditis elegans tha

A mutation in Caenorhabditis elegans that increases recombination frequency more than threefold

✍ Rose, A. M.; Baillie, D. L. 📂 Article 📅 1979 🏛 Nature Publishing Group 🌐 English ⚖ 241 KB

A heteroplasmic mitochondrial complex I

A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia

✍ David K. Simon; Jennifer Friedman; Xandra O. Breakefield; Joseph Jankovic; Mitch 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 155 KB

De novo mutations in the mitochondrial N

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

✍ Robert McFarland; Denise M. Kirby; Kerry J. Fowler; Akira Ohtake; Michael T. Rya 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 226 KB 👁 2 views

Evidence for complex nuclear inheritance

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

✍ Bykhovskaya, Yelena; Shohat, Mordechai; Ehrenman, Karen; Johnson, David; Hamon, 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 25 KB 👁 2 views

The relationship between mitochondrial genotype and clinical phenotype is complicated in most instances by the heteroplasmic nature of pathogenic mitochondrial mutations. We have previously shown that maternally inherited hearing loss in a large Arab-Israeli kindred is due to the homoplasmic A1555G

A novel mutation in the mitochondrial tR

A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

✍ Da Pozzo, Paola; Cardaioli, Elena; Malfatti, Edoardo; Gallus, Gian Nicola; Malan 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 171 KB