Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair
about
Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair geneTAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemiaSite-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemiaThe tal gene undergoes chromosome translocation in T cell leukemia and potentially encodes a helix-loop-helix proteinHEN1 and HEN2: a subgroup of basic helix-loop-helix genes that are coexpressed in a human neuroblastomaLigation-independent cloning of PCR products (LIC-PCR)Ubiquitous mitochondrial creatine kinase downregulated in oral squamous cell carcinoma.Identification of new DNA markers close to the myotonic dystrophy locus.Coincidence cloning of Alu PCR products.A study of DNA methylation in myotonic dystrophy.Molecular cloning, expression, and chromosome 19 localization of a human Ro/SS-A autoantigen.An informative panel of somatic cell hybrids for physical mapping on human chromosome 19qD19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusDe novo myotonic dystrophy mutation in a Nigerian kindred.Modulation of gene activity by consecutive gene targeting of one creatine kinase M allele in mouse embryonic stem cells.Segregation distortion of the CTG repeats at the myotonic dystrophy locus.The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.NcoI RFLP at 19q13 identified by the DNA sequence pW119B (D19S169).RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63).A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245).A polymorphic DNA clone which maps to 19q13.2-19qter (D19S62).MspI RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112).Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.
P2860
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P2860
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair
description
1988 nî lūn-bûn
@nan
1988 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Human creatine kinase genes on ...... protein C2 and excision repair
@ast
Human creatine kinase genes on ...... protein C2 and excision repair
@en
Human creatine kinase genes on ...... protein C2 and excision repair
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type
label
Human creatine kinase genes on ...... protein C2 and excision repair
@ast
Human creatine kinase genes on ...... protein C2 and excision repair
@en
Human creatine kinase genes on ...... protein C2 and excision repair
@nl
prefLabel
Human creatine kinase genes on ...... protein C2 and excision repair
@ast
Human creatine kinase genes on ...... protein C2 and excision repair
@en
Human creatine kinase genes on ...... protein C2 and excision repair
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P2093
P2860
P1476
Human creatine kinase genes on ...... protein C2 and excision repair
@en
P2093
A W Strauss
L H Thompson
L L Bachinski
M J Siciliano
R L Stallings
P2860
P304
P407
P577
1988-08-01T00:00:00Z