High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization
about
The human collagen X gene. Complete primary translated sequence and chromosomal localizationTargeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15Interferon-inducible gene maps to a chromosomal band associated with a (4;11) translocation in acute leukemia cellsIsolation of a cDNA clone and localization of human glutathione S-transferase 2 genes to chromosome band 6p12Assignment of the human and mouse prion protein genes to homologous chromosomesConcerted evolution of human amylase genesA truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignmentConstruction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transferLocalization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locusAssignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1Purification and properties of human cytosolic folylpoly-gamma-glutamate synthetase and organization, localization, and differential splicing of its geneMuscular dystrophy in girls with X;autosome translocations.Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomesHuman nuclear NAD+ ADP-ribosyltransferase: localization of the gene on chromosome 1q41-q42 and expression of an active human enzyme in Escherichia coliArray-CGH and quantitative PCR genetic analysis in a case with bilateral hypoplasia of pulmonary arteries and lungs and simultaneous unilateral renal agenesis.Identification of POMC exonic variants associated with substance dependence and body mass indexExon-intron organization, expression, and chromosomal localization of the human motilin gene.Primary structure of c-kit: relationship with the CSF-1/PDGF receptor kinase family--oncogenic activation of v-kit involves deletion of extracellular domain and C terminus.The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23.Chromosome deletion mapping of interspersed low-copy repetitive DNAFurther evidence for the dispersion of the human fibrillar collagen genes.The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1.5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.Assignment of the gene for the beta subunit of thyroid-stimulating hormone to the short arm of human chromosome 1.Integration of papillomavirus DNA near myc genes in genital carcinomas and its consequences for proto-oncogene expression.Protein tyrosine phosphatase containing SH2 domains: characterization, preferential expression in hematopoietic cells, and localization to human chromosome 12p12-p13.Amylase-producing ovarian carcinoma: A case report and a retrospective study.Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor.Genetics of human salivary proteins.Ectopic hormone syndromes.Isolation and characterization of mouse dishevelled-3.Two human myeloma cell lines, amylase-producing KMS-12-PE and amylase-non-producing KMS-12-BM, were established from a patient, having the same chromosome marker, t(11;14)(q13;q32).Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22.The calcitonin-like sequence of the beta CGRP gene.The structural gene for aldolase B (ALDB) maps to 9q13?32Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (?-FNR) to chromosome 10p11.2
P2860
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P2860
High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization
description
1983 nî lūn-bûn
@nan
1983 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1983 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
name
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@ast
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@en
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@nl
type
label
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@ast
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@en
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@nl
prefLabel
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@ast
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@en
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@nl
P2093
P2860
P356
P1476
High-resolution chromosomal lo ...... D3S1) by in situ hybridization
@en
P2093
A Y Sakaguchi
S L Naylor
P2860
P304
P356
10.1073/PNAS.80.22.6932
P407
P577
1983-11-01T00:00:00Z