Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P36941 (
Lymphotoxin-beta receptor
)
12
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We have constructed a physical map of a 4.6-cM region of human chromosome band 12p13.3 that contains a translocation breakpoint from a
mesothelioma
with a t(X;12)(q22;p13). The map contains a contig of 22 yeast artificial chromosomes (YACs), onto which we have placed 18 sequence tagged site (STS) markers, including seven genes:
D12S370
, FGF6, KCAN1, KCNA5, KCNA6, NTF3, and VWF. A second YAC contig, comprised of 22 YAC clones, was located distal to the
mesothelioma
breakpoint and contained 12 STS markers, including four genes (CACNL1A1, D12S380E, D12S381E, and D12S382E). Based on STS content and fluorescence in situ hybridization experiments, two stable, nonchimeric YAC clones were found that span the
mesothelioma
breakpoint. A long-range restriction map of an 800-kb region was constructed and used to refine the
mesothelioma
breakpoint to a region of approximately 100 kb, flanked by the potassium channel genes KCNA1 and KCNA5. The latter was confirmed by direct visual hybridization (DIRVISH) experiments, using cosmids isolated for markers flanking the breakpoint as probes.
...
PMID:A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13). 758 92
Two somatic cell hybrids containing the der(12) or the der(X) from a
mesothelioma
with a translocation t(X;12)(q22;p13) as the only chromosomal change were generated to characterize the region of 12p13 containing the translocation breakpoint. Fluorescence in situ hybridization analysis showed the breakpoint on chromosome 12 to occur between VWF and D12S158. On the linkage map developed by J. Weissenbach et al. (Nature, 1992, 359: 794-801), the breakpoints were located between D12S99 and D12S100 on chromosome 12 and between DXS1106 and DXS1001 on chromosome X. PCR analysis based on genomic sequences, with DNA from both somatic cell hybrids, enabled us to map CACNL1A1, FGF6,
D12S370
, D12S38OE, D12S381E, and D12S382E distally to the 12p13 breakpoint and to VWF.
...
PMID:Regional assignment of seven loci to 12p13.2-pter by PCR analysis of somatic cell hybrids containing the der(12) or the der(X) chromosome from a mesothelioma showing t(X;12)(q22;p13). 802 Sep 38