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19 Possible Causes for (S, RAD23a, homolog

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  • Xeroderma Pigmentosum Complementation Group C

    […] are functional homologs.[ncbi.nlm.nih.gov] Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A.[genecards.org] -I. and Haga, T. and Aiba, S. Case Reports in Dermatology. 2013; 5(1): 64-68 [Pubmed][ijmpo.org]

  • Xeroderma Pigmentosum Complementation Group B

    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] Cerevisiae)): RAD23A antibodies RAD23A Proteins RAD23B - RAD23 Homolog B (S.[antibodies-online.com] F. , Keeney , S. , Smith , C. A. , Taylor , J. S. , Linn , S. & Sancar , A. ( 1993 ).[cambridge.org]

  • Wiedemann-Rautenstrauch Syndrome

    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] XPA, XPB, XPC, XPD, XPE, XPF, additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others also participate in nucleotide excision repair.[wikivisually.com] […] 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]

  • Cerebro-Oculo-Facio-Skeletal Syndrome

    Double-strand breaks can be repaired through homologous recombination or through non-homologous end joining, NHEJ is a DNA repair mechanism which, unlike homologous recombination[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]

  • Progressive External Ophthalmoplegia - Myopathy - Emaciation Syndrome

    […] hg38-Dec_2013) GoldenPath hg19 (UCSC) MGME1 - 20p11.23 [Description] (hg19-Feb_2009) Ensembl MGME1 - 20p11.23 [CytoView hg19] MGME1 - 20p11.23 [CytoView hg38] Mapping of homologs[atlasgeneticsoncology.org] ATR BRCA1 BRCA2 CHEK2 ERCC2 GADD45A HSPA1A MLH1 MSH3 NBN OGG1 PARP1 PRKDC RAD23B SIRT1 XRCC1 Stomach Neoplasms APEX1 ATM CHEK2 DDB1 ERCC1 ERCC2 GADD45A MUTYH NPM1 PRPF19 RAD23A[selfdecode.com] Schöler, AP Kudin, S Vielhaber, ...[scholar.google.de]

  • Xeroderma Pigmentosum-Cockayne Syndrome Complex

    Summary Homologous recombination is a major double-strand break (DSB) repair mechanism that acts during the S and G2 phases.[scinapse.io] Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A.[genecards.org] F. , Keeney S. , Smith C. A. , Taylor J. S. , Linn S. & Sancar A. ( 1993 ).[cambridge.org]

  • Cerebro-Oculo-Facio-Skeletal Syndrome 1

    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] XPA, XPB, XPC, XPD, XPE, XPF, additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others also participate in nucleotide excision repair.[wikivisually.com] S).[pnas.org]

  • UV-Sensitive Syndrome 1

    […] recombination Top of Page RAD51 Homologous pairing 15q15.1 NM_002875 RAD51B Rad51 homolog 14q24.1 NM_002877 RAD51D Rad51 homolog 17q12 NM_002878 DMC1 Rad51 homolog, meiosis[mdanderson.org] Two complementation groups have been identified among UV S S patient s, defined by mutation s in an as-yet-unidentified Author contributions: G.S., A.[yumpu.com] A DNA repair gene of Caenorhabditis elegans : a homolog of human XPF. DNA Repair(Amst). 3 , 1375–1383.[wormbook.org]

  • CAMFAK Syndrome

    Double-strand breaks can be repaired through homologous recombination or through non-homologous end joining, NHEJ is a DNA repair mechanism which, unlike homologous recombination[wikivisually.com] Presentation The name "CAMFAK" comes from the first letters of the characteristic findings of the disease: ca taract s, m icrocephaly , fa ilure to thrive , and k yphoscoliosis[en.academic.ru] Alessandro Castriota-Scanderbeg the possible the pattern of inheritance.This approach to the s- publication of this book.[books.google.com]

  • Disorder of Pyrimidine Metabolism

    The enzyme that catalyzes this addition, pyrimidine phosphoribosyl transferase, is homologous to a number of other phosphoribosyl transferases that add different groups to[namrata.co] 89 AGA 7 SSR2, FAR1, NOL12, NAV1, TRIOBP, SCCPDH, HSP90B1 75 HPRT1 5 SF1, MARS, TCEA2, ANKRD13A, PHF13 73 HPRT1 6 LPP, SKIL, ZNF281, PDLIM7, COL1A2, AMIGO2, STUB1, CD44, RAD23A[ojrd.biomedcentral.com] This X-linked recessive disorder is associated with reduced sensitivity of PPRP-S to nucleotide inhibition and increased specific activity of PPRP-S in vitro.[musculoskeletalkey.com]