A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice
about
Oxidative stress, mitochondrial dysfunction, and agingFunctional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Knockout of the transcription factor NRF2 disrupts spermatogenesis in an age-dependent mannerDeficiency in the inner mitochondrial membrane peptidase 2-like (Immp21) gene increases ischemic brain damage and impairs mitochondrial functionMitochondrial peptidase IMMP2L mutation causes early onset of age-associated disorders and impairs adult stem cell self-renewalMitochondrial protein Fus1/Tusc2 in premature aging and age-related pathologies: critical roles of calcium and energy homeostasisGenetic associations for keratoconus: a systematic review and meta-analysis.Differential Evolution between Monotocous and Polytocous Species.Mitochondrial mechanisms in cerebral vascular control: shared signaling pathways with preconditioning.Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors.Transcriptomic profiling of proteases and antiproteases in the liver of sexually mature hens in relation to vitellogenesisExamination of bioenergetic function in the inner mitochondrial membrane peptidase 2-like (Immp2l) mutant mice.Chromosomal abnormalities & oxidative stress in women with premature ovarian failure (POF)Genome-Wide Analysis of Acute Endurance Exercise-Induced Translational Regulation in Mouse Skeletal Muscle.Oxidative stress is involved in age-dependent spermatogenic damage of Immp2l mutant miceAnalysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family StudyThe Immp2l mutation causes age-dependent degeneration of cerebellar granule neurons prevented by antioxidant treatment.Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.Superoxide overproduction and kidney fibrosis: a new animal model.Bladder dysfunction in a new mutant mouse model with increased superoxide--lack of nitric oxide?Reproductive switching analysis of Daphnia similoides between sexual female and parthenogenetic female by transcriptome comparison.The role of nitric oxide signaling in food intake; insights from the inner mitochondrial membrane peptidase 2 mutant mice.The mammalian ovary from genesis to revelation.Mitochondrial and sex steroid hormone crosstalk during aging.Studies of genomic copy number changes in human cancers reveal signatures of DNA replication stressRodent models for urodynamic investigation.New roles for mitochondrial proteases in health, ageing and disease.Genetic influences on the human oral microbiomeMitochondria-targeted antioxidant SkQ1 improves spermatogenesis in Immp2l mutant mice.Genetics of mitochondrial dysfunction and infertility.Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders.Genome-wide association with delayed puberty in swine.Oxidative stress and its possible relation to lower urinary tract functional pathology.A Role for Respiration in Regulating Meiosis Initiation in Saccharomyces cerevisiae.Substrain- and sex-dependent differences in stroke vulnerability in C57BL/6 mice.Suppression of Inner Mitochondrial Membrane Peptidase 2-Like (IMMP2L) Gene Exacerbates Hypoxia-Induced Neural Death Under High Glucose Condition.Role of Mitochondria in Cerebral Vascular Function: Energy Production, Cellular Protection, and Regulation of Vascular Tone.Nucleotide variations in mitochondrial DNA and supra-physiological ROS levels in cytogenetically normal cases of premature ovarian insufficiency.Triangle Consortium for Reproductive Biology 22nd Annual Meeting.
P2860
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P2860
A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice
description
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2008
@ast
im Dezember 2007 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
@en
vedecký článok (publikovaný 2008/04/01)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/04/01)
@nl
наукова стаття, опублікована у квітні 2008
@uk
مقالة علمية (نشرت في أبريل 2008)
@ar
name
A mutation in the inner mitoch ...... and impairs fertility in mice
@ast
A mutation in the inner mitoch ...... and impairs fertility in mice
@en
A mutation in the inner mitoch ...... and impairs fertility in mice
@nl
type
label
A mutation in the inner mitoch ...... and impairs fertility in mice
@ast
A mutation in the inner mitoch ...... and impairs fertility in mice
@en
A mutation in the inner mitoch ...... and impairs fertility in mice
@nl
prefLabel
A mutation in the inner mitoch ...... and impairs fertility in mice
@ast
A mutation in the inner mitoch ...... and impairs fertility in mice
@en
A mutation in the inner mitoch ...... and impairs fertility in mice
@nl
P2093
P2860
P3181
P1476
A mutation in the inner mitoch ...... and impairs fertility in mice
@en
P2093
Christian Gratzke
Christophe Poirier
Colin E Bishop
David Busija
Karl-Erik Andersson
Martin M Matzuk
Tamas Gaspar
Wilbur Harrison
P2860
P304
P3181
P356
10.1095/BIOLREPROD.107.065987
P407
P577
2007-12-19T00:00:00Z