Xeroderma Pigmentosum, Complementation Group B (XP-B) ELISA Kits

Bezeichnung:
Xeroderma Pigmentosum, Complementation Group B ELISA Kits (XP-B)
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Synonyme:
BTF2, GTF2H, RAD25, TFIIH, XPB
list all ELISA KIts Gen GeneID UniProt
Human XP-B XP-B 2071 P19447

Weitere Synonyme anzeigen

Weitere ELISA Kits für Xeroderma Pigmentosum, Complementation Group B Interaktionspartner

Human Xeroderma Pigmentosum, Complementation Group B (XP-B) Interaktionspartner

  1. significant interactions between ERCC2 (zeige ERCC2 ELISA Kits) (Lys751Gln) and ERCC3 (zeige ERCC3 ELISA Kits) (7122 A>G) genotypes polymorphism and cadmium exposure in association with nasal polyposis disease

  2. Data did not find any association between ERCC2 (zeige ERCC2 ELISA Kits) or ERCC3 (zeige ERCC3 ELISA Kits) gene polymorphisms and the development of osteosarcoma.

  3. Transcriptional differences found between various TFIIH subunit variants participate in the phenotypic variability observed among xeroderma pigmentosum, XP associated with Cockayne syndrome, and trichothiodystrophy individuals.

  4. XPB (zeige GTF2H5 ELISA Kits) and XPD (zeige ERCC2 ELISA Kits) enrichment at G4 motifs characterizes specific signaling pathways and regulatory pathways associated with specific cancers

  5. findings suggest that benzene exposure may be associated with hypermethylation in ERCC3 (zeige ERCC3 ELISA Kits), and that genetic variants in EPHX1 (zeige EPHX1 ELISA Kits) may play an important role in epigenetic changes and hematotoxicity among benzene-exposed workers

  6. The crystal structure of the C-terminal half of the XPB (zeige GTF2H5 ELISA Kits) subunit of TFIIH (zeige GTF2H1 ELISA Kits) (residues 494-782) is reported, containing XPB (zeige GTF2H5 ELISA Kits) helicase domain (HD)2 (zeige HDAC2 ELISA Kits) and a C-terminal extension which shares structural similarity with RIG-I (zeige DDX58 ELISA Kits).

  7. results identify the ARCH domain of XPD (zeige ERCC2 ELISA Kits) as a platform for the recruitment of CAK (zeige CCNH ELISA Kits) and as a molecular switch that might control TFIIH (zeige GTF2H1 ELISA Kits) composition and play a role in conversion of TFIIH (zeige GTF2H1 ELISA Kits) from a factor active in transcription to a factor involved in DNA repair

  8. XPB (zeige GTF2H5 ELISA Kits) and XPD (zeige ERCC2 ELISA Kits) helicases differentially regulate TFIIH (zeige GTF2H1 ELISA Kits) compositional change during nucleotide excision repair.

  9. Phenotype-specific adverse effects of XPD (zeige ERCC2 ELISA Kits) mutations on human prenatal development implicate impairment of TFIIH (zeige GTF2H1 ELISA Kits)-mediated functions in placenta.

  10. reduction in ERCC3 (zeige ERCC3 ELISA Kits) by siRNA interference in human melanocytes in vitro reduced their tyrosinase (zeige TYR ELISA Kits) production ability

Xeroderma Pigmentosum, Complementation Group B (XP-B) Antigen-Profil

Beschreibung des Gens

ERCC3 is an ATP-dependent DNA helicase that functions in nucleotide excision repair and complements xeroderma pigmentosum group B mutations. It also is the 89 kDa subunit of basal transcription factor 2 (TFIIH) and thus functions in class II transcription.

Alternative names and synonyms associated with Xeroderma Pigmentosum, Complementation Group B (XP-B)

  • excision repair cross-complementing rodent repair deficiency, complementation group 3 (ERCC3) Elisa Kit
  • BTF2 Elisa Kit
  • GTF2H Elisa Kit
  • RAD25 Elisa Kit
  • TFIIH Elisa Kit
  • XPB Elisa Kit

Bezeichner auf Proteinebene für XP-B

BTF2 p89 , DNA excision repair protein ERCC-3 , DNA repair protein complementing XP-B cells , TFIIH 89 kDa subunit , TFIIH basal transcription factor complex 89 kDa subunit , TFIIH basal transcription factor complex helicase XPB subunit , TFIIH p89 , basic transcription factor 2 89 kDa subunit , xeroderma pigmentosum group B-complementing protein , xeroderma pigmentosum, complementation group B

GENE ID SPEZIES
2071 Homo sapiens
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