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34 Possible Causes for (S, RAD23b, homolog

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  • Xeroderma Pigmentosum Complementation Group C

    This human protein of 940 residues forms a strong heterotrimeric complex with Rad23B and centrin 2.[ncbi.nlm.nih.gov] […] are functional homologs.[ncbi.nlm.nih.gov] -I. and Haga, T. and Aiba, S. Case Reports in Dermatology. 2013; 5(1): 64-68 [Pubmed][ijmpo.org]

  • Xeroderma Pigmentosum Complementation Group B

    Cerevisiae): RAD23B antibodies RAD23B ELISA Kits RAD23B Proteins CETN2 (Centrin, EF-Hand Protein, 2): CETN2 antibodies CETN2 Proteins DDB2 (Damage-Specific DNA Binding Protein[antibodies-online.com] The flanking probe strategy selects for long stretches of nucleotide sequence homology, and avoids isolation of small regions with fortuitous homology.[ncbi.nlm.nih.gov] F. , Keeney , S. , Smith , C. A. , Taylor , J. S. , Linn , S. & Sancar , A. ( 1993 ).[cambridge.org]

  • Xeroderma Pigmentosum

    Mutations in the XPB(ERCC3) gene can lead to XP or XP combined with Cockayne syndrome . [10] The XPC protein forms a complex with RAD23B protein to form the initial damage[en.wikipedia.org] We, particularly, developed the correction of XP-C skin cells using the fidelity of the homologous recombination pathway during repair of double-strand break (DSB) in the[ncbi.nlm.nih.gov] Fe-S proteins including XPD.[ncbi.nlm.nih.gov]

  • Wiedemann-Rautenstrauch Syndrome

    XPA, XPB, XPC, XPD, XPE, XPF, additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others also participate in nucleotide excision repair.[wikivisually.com] Seite 86 - Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 1996;85: 841-851. ‎[books.google.de] […] t u v w x y z BROWSE medications a b c d e f g h i j k l m n o p q r s t u v w x y z[drdoleary.com]

  • Xeroderma

    Mutations in the XPB(ERCC3) gene can lead to XP or XP combined with Cockayne syndrome . [13] The XPC protein forms a complex with RAD23B protein to form the initial damage[en.wikipedia.org] The repair mechanisms for UV rays are nucleotide excision repair and translesion synthesis while for X-rays, they are base excision repair, homologous recombination, and nonhomologous[ncbi.nlm.nih.gov] F. , Keeney , S. , Smith , C. A. , Taylor , J. S. , Linn , S. & Sancar , A. ( 1993 ).[cambridge.org]

  • Setleis Syndrome

    […] protein 2 1.60602 RTTN rotatin 1.60602 ORC3 origin recognition complex, subunit 3 1.60601 SMG6 SMG6 nonsense mediated mRNA decay factor 1.60298 RAD51C RAD51 paralog C 1.59796 RAD23B[amp.pharm.mssm.edu] In patients with no duplication/triplication of the 1p36.22p36.21 region and no mutations in TWIST2, there are mutation(s) in one of the 30 genes in this region or mutations[ncbi.nlm.nih.gov] The extract was collected and analyzed by Fourier-transform infrared s...[medworm.com]

  • Squamous Cell Carcinoma of the Head and Neck

    ., Laryngeal cancer risk associated with smoking and alcohol consumption is modified by genetic polymorphisms in ERCC5, ERCC6 and RAD23B but not by polymorphisms in five other[degruyter.com] In HNSCC and cervical cancer, there was significant enrichment for homologous recombination genes.[ncbi.nlm.nih.gov] According to the importance of CDC6 and CDK2 for G1 to S transition, WHSC1L1 knockdown induced strong G0/G1 arrest which was rescued by introduction of wild-type WHSC1L1 but[ncbi.nlm.nih.gov]

  • Cerebro-Oculo-Facio-Skeletal Syndrome

    XPA, XPB, XPC, XPD, XPE, XPF, additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others also participate in nucleotide excision repair.[wikivisually.com] At 12 months his head circumference was - 6.5 S. D., and at 18 and 26 months, - 7.0 S. D. and - 7.5 S. D. The figures for length were -4.5 S. D., -5 .5 S.[myslide.es] "DNA damage during the G0/G1 phase triggers RNA-templated, Cockayne syndrome B-dependent homologous recombination" . Proc. Natl. Acad. Sci.[en.wikipedia.org]

  • Xeroderma Pigmentosum Variant

    Mutations in the XPB(ERCC3) gene can lead to XP or XP combined with Cockayne syndrome . [13] The XPC protein forms a complex with RAD23B protein to form the initial damage[en.wikipedia.org] We suggest that this mutation POLH NG_009252.1: g.36847_40771del3925 is caused by an equal crossover event that occurred between two homologous chromosomes at meiosis.[ncbi.nlm.nih.gov] In this study the effects of UVC on S phase cells were compared in fibroblasts derived from normal donors (IDH4) and XP-V patients (CTag) and immortalized by expression of[ncbi.nlm.nih.gov]

  • Cerebro-Oculo-Facio-Skeletal Syndrome 1

    XPA, XPB, XPC, XPD, XPE, XPF, additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others also participate in nucleotide excision repair.[wikivisually.com] 115 Telomeres and DNA Repair Factors 116 Nonhomologous End Joining NHEJ Complex and Telomeres 117 PARP1 and Telomeres 120 Concerted Roles of PARP1 and p53 on Telomeres 122 Homologous[books.google.com] S).[pnas.org]