Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality
about
Dynamic interaction of TTDA with TFIIH is stabilized by nucleotide excision repair in living cellsDisruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethalityMore than blood, a novel gene required for mammalian postimplantation developmentConnecting the Dots: From DNA Damage and Repair to AgingDisease-causing missense mutations in human DNA helicase disordersReduced life- and healthspan in mice carrying a mono-allelic BubR1 MVA mutationRescue of progeria in trichothiodystrophy by homozygous lethal Xpd allelesEarly embryonic lethality due to targeted inactivation of DNA ligase IIIPostnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G geneAn Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.Relationship between XPD Lys 751 Gln polymorphism and colorectal cancer risk: a case-control study in a population-based studyHydrogen peroxide induced genomic instability in nucleotide excision repair-deficient lymphoblastoid cellsMale infertility and DNA damage in Doppel knockout and prion protein/Doppel double-knockout miceXPD localizes in mitochondria and protects the mitochondrial genome from oxidative DNA damage.The Polymerase Activity of Mammalian DNA Pol ζ Is Specifically Required for Cell and Embryonic Viability.Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer.DNA-damage repair; the good, the bad, and the ugly.XPD-dependent activation of apoptosis in response to triplex-induced DNA damage.Archaeal genome guardians give insights into eukaryotic DNA replication and damage response proteins.Genetic correction of stem cells in the treatment of inherited diseases and focus on xeroderma pigmentosum.DNA repair and transcriptional effects of mutations in TFIIH in Drosophila development.Cdk8 is essential for preimplantation mouse development.Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue.A Drosophila XPD model links cell cycle coordination with neuro-development and suggests links to cancer.Optical Control of DNA Helicase Function through Genetic Code Expansion.
P2860
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P2860
Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
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1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
name
Disruption of the mouse xerode ...... s in preimplantation lethality
@ast
Disruption of the mouse xerode ...... s in preimplantation lethality
@en
Disruption of the mouse xerode ...... s in preimplantation lethality
@nl
type
label
Disruption of the mouse xerode ...... s in preimplantation lethality
@ast
Disruption of the mouse xerode ...... s in preimplantation lethality
@en
Disruption of the mouse xerode ...... s in preimplantation lethality
@nl
prefLabel
Disruption of the mouse xerode ...... s in preimplantation lethality
@ast
Disruption of the mouse xerode ...... s in preimplantation lethality
@en
Disruption of the mouse xerode ...... s in preimplantation lethality
@nl
P2093
P3181
P1433
P1476
Disruption of the mouse xerode ...... s in preimplantation lethality
@en
P2093
P3181
P407
P577
1998-01-01T00:00:00Z