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hereafter x Genetics and Genomics x clear all


Overview page. Subjects: Biblical Studies.

Used by AV with the meaning ‘at some future time’ in John 13: 7 where NRSV and NJB have ‘later’, REB ‘one day’. At Matt. 26: 64 NRSV and REB have ‘from now on’, and NJB ‘from this time...

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Genetic analysis of variation for auxin-induced adventitious root formation among eighteen ecotypes of <i>Arabidopsis thaliana</i> L. Heynh.

JJ King and DP Stimart.

in Journal of Heredity

November 1998; p ublished online November 1998 .

Journal Article. Subjects: Genetics and Genomics. 0 words.

Eighteen ecotypes and two inbred lines of Arabidopsis thaliana L. Heynh. were analyzed for variation in the number of adventitious roots formed (hereafter referred to as rooting) on...

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<i>Gpr126/Adgrg6</i> deletion in cartilage models idiopathic scoliosis and pectus excavatum in mice

Courtney M. Karner, Fanxin Long, Lilianna Solnica-Krezel, Kelly R. Monk and Ryan S. Gray.

in Human Molecular Genetics

August 2015; p ublished online May 2015 .

Journal Article. Subjects: Genetics and Genomics. 5334 words.

Adolescent idiopathic scoliosis (AIS) and pectus excavatum (PE) are common pediatric musculoskeletal disorders. Little is known about the tissue of origin for either condition, or about...

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Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy

Olga Criado, Carmen Aguado, Javier Gayarre, Lara Duran-Trio, Ana M. Garcia-Cabrero, Santiago Vernia, Beatriz San Millán, Miguel Heredia, Carlos Romá-Mateo, Silvana Mouron, Lucía Juana-López, Mercedes Domínguez, Carmen Navarro, Jose M. Serratosa, Marina Sanchez, Pascual Sanz, Paola Bovolenta, Erwin Knecht and Santiago Rodriguez de Cordoba.

in Human Molecular Genetics

April 2012; p ublished online December 2011 .

Journal Article. Subjects: Genetics and Genomics. 7220 words.

Lafora disease (LD), a fatal neurodegenerative disorder characterized by the presence of intracellular inclusions called Lafora bodies (LBs), is caused by loss-of-function mutations in...

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Genetic Control of Floral Morph in Tristylous Pickerelweed (<i>Pontederia cordata</i> L.)

Lyn A. Gettys and David S. Wofford.

in Journal of Heredity

January 2008; p ublished online May 2008 .

Journal Article. Subjects: Genetics and Genomics. 3222 words.

Pickerelweed (Pontederia cordata L.) is a diploid (2n = 2x = 16) tristylous aquatic perennial. Populations usually contain 3 floral morphs that differ reciprocally in style length and...

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A mutation in the human <i>CBP4</i> ortholog <i>UQCC3</i> impairs complex III assembly, activity and cytochrome <i>b</i> stability

Bas F.J. Wanschers, Radek Szklarczyk, Mariël A.M. van den Brand, An Jonckheere, Janneke Suijskens, Roel Smeets, Richard J. Rodenburg, Katharina Stephan, Ingrid B. Helland, Areej Elkamil, Terje Rootwelt, Martin Ott, Lambert van den Heuvel, Leo G. Nijtmans and Martijn A. Huynen.

in Human Molecular Genetics

December 2014; p ublished online July 2014 .

Journal Article. Subjects: Genetics and Genomics. 5822 words.

Complex III (cytochrome bc1 ) is a protein complex of the mitochondrial inner membrane that transfers electrons from ubiquinol to cytochrome c. Its assembly requires the...

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PINK1 rendered temperature sensitive by disease-associated and engineered mutations

Derek P. Narendra, Chunxin Wang, Richard J. Youle and John E. Walker.

in Human Molecular Genetics

July 2013; p ublished online March 2013 .

Journal Article. Subjects: Genetics and Genomics. 11793 words.

Mutations in Parkin or PINK1 are the most common cause of recessively inherited parkinsonism. Parkin and PINK1 function in a conserved mitochondrial quality control pathway, in which PINK1,...

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CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in <i>Saccharomyces cerevisiae</i>

Bala S. Balakumaran, Catherine H. Freudenreich and Virginia A. Zakian.

in Human Molecular Genetics

January 2000; p ublished online January 2000 .

Journal Article. Subjects: Genetics and Genomics. 6914 words.

An expansion to >200 CGG/CCG repeats (hereafter called CGG) in the 5′ region of the FMR1 gene causes fragile X syndrome, and this locus becomes a folate-sensitive fragile site. We used Sacch...

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Recommendations for conducting the <i>in vivo</i> alkaline Comet assay

A. Hartmann, E. Agurell, C. Beevers, S. Brendler-Schwaab, B. Burlinson, P. Clay, A. Collins, A. Smith, G. Speit, V. Thybaud and R.R. Tice.

in Mutagenesis

January 2003; p ublished online January 2003 .

Journal Article. Subjects: Clinical Cytogenetics and Molecular Genetics; Genetics and Genomics. 6244 words.

The in vivo alkaline single cell gel electrophoresis assay, hereafter the Comet assay, can be used to investigate the genotoxicity of industrial chemicals, biocides, agrochemicals and...

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Clustering of Two Genes Putatively Involved in Cyanate Detoxification Evolved Recently and Independently in Multiple Fungal Lineages

M. Holly Elmore, Kriston L. McGary, Jennifer H. Wisecaver, Jason C. Slot, David M. Geiser, Stacy Sink, Kerry O’Donnell and Antonis Rokas.

in Genome Biology and Evolution

P ublished online February 2015 .

Journal Article. Subjects: Bioinformatics and Computational Biology; Evolutionary Biology; Genetics and Genomics. 6240 words.

Fungi that have the enzymes cyanase and carbonic anhydrase show a limited capacity to detoxify cyanate, a fungicide employed by both plants and humans. Here, we describe a novel two-gene...

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TEFM (c17orf42) is necessary for transcription of human mtDNA

Michal Minczuk, Jiuya He, Anna M. Duch, Thijs J. Ettema, Aleksander Chlebowski, Karol Dzionek, Leo G. J. Nijtmans, Martijn A. Huynen and Ian J. Holt.

in Nucleic Acids Research

May 2011; p ublished online January 2011 .

Journal Article. Subjects: Chemistry; Biochemistry; Bioinformatics and Computational Biology; Genetics and Genomics; Molecular and Cell Biology. 8780 words.

Here we show that c17orf42, hereafter TEFM (transcription elongation factor of mitochondria), makes a critical contribution to mitochondrial transcription. Inactivation of TEFM in cells by...

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