Molecular analysis of cloned human 18S ribosomal DNA segments.
about
Human 18 S ribosomal RNA sequence inferred from DNA sequence. Variations in 18 S sequences and secondary modification patterns between vertebratesCharacterization of a human cDNA encoding a widely expressed and highly conserved cysteine-rich protein with an unusual zinc-finger motifHuman ribosomal RNA gene: nucleotide sequence of the transcription initiation region and comparison of three mammalian genesIsolation of novel non-HLA gene fragments from the hemochromatosis region (6p21.3) by cDNA hybridization selectionA new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations.A transforming growth factor beta (TGFbeta) control element drives TGFbeta-induced stimulation of smooth muscle alpha-actin gene expression in concert with two CArG elements.Construction of a uniform-abundance (normalized) cDNA library.cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments.mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisA molecular basis for discrete size variation in human ribosomal DNA.Structure and variation of human ribosomal DNA: the external transcribed spacer and adjacent regions.HeLa cell identification by analysis of ribosomal DNA segment patterns generated by endonuclease restriction.Delineation of a human histone H4 cell cycle element in vivo: the master switch for H4 gene transcription.Functional and structural features of a tandem duplication of the human mtDNA promoter region.Cloning and determination of the transcription termination site of ribosomal RNA gene of the mouseFractionation and reconstitution of factors required for accurate transcription of mammalian ribosomal RNA genes: identification of a species-dependent initiation factor.A family of long reiterated DNA sequences, one copy of which is next to the human beta globin geneMitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures.Molecular characterization of de novo secondary trisomy 13.Supercoil induced S1 hypersensitive sites in the rat and human ribosomal RNA genes.Human nucleolus organizers on nonhomologous chromosomes can share the same ribosomal gene variants.Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes.In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human delta and beta globin genesMouse beta-globin DNA-binding protein B1 is identical to a proto-oncogene, the transcription factor Spi-1/PU.1, and is restricted in expression to hematopoietic cells and the testisHuman ribosomal DNA fragments amplified in hamster cells are transcribed only by RNA polymerase II and are not silver stained.Formation of the transcription initiation complex on mammalian rDNA.Developmental regulation of collagenase-3 mRNA in normal, differentiating osteoblasts through the activator protein-1 and the runt domain binding sites.Expression of the transcription factor, Spi-1 (PU.1), in differentiating murine erythroleukemia cells Is regulated post-transcriptionally. Evidence for differential stability of transcription factor mRNAs following inducer exposure.A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn).The carboxyl-terminal domain of the granulocyte colony-stimulating factor receptor uncouples ribosomal biogenesis from cell cycle progression in differentiating 32D myeloid cells.Detection of a proliferation specific gene during development of the osteoblast phenotype by mRNA differential display.Functional and molecular mitochondrial abnormalities associated with a C --> T transition at position 3256 of the human mitochondrial genome. The effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing.Clones of human ribosomal DNA containing the complete 18 S-rRNA and 28 S-rRNA genes. Characterization, a detailed map of the human ribosomal transcription unit and diversity among clones.Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints.Regulation of collagenase-3 and osteocalcin gene expression by collagen and osteopontin in differentiating MC3T3-E1 cells.Enhanced levels of cathepsin B mRNA in murine tumors.
P2860
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P2860
Molecular analysis of cloned human 18S ribosomal DNA segments.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh
1978年學術文章
@zh-hant
name
Molecular analysis of cloned human 18S ribosomal DNA segments.
@en
Molecular analysis of cloned human 18S ribosomal DNA segments.
@nl
type
label
Molecular analysis of cloned human 18S ribosomal DNA segments.
@en
Molecular analysis of cloned human 18S ribosomal DNA segments.
@nl
prefLabel
Molecular analysis of cloned human 18S ribosomal DNA segments.
@en
Molecular analysis of cloned human 18S ribosomal DNA segments.
@nl
P2093
P2860
P356
P1476
Molecular analysis of cloned human 18S ribosomal DNA segments.
@en
P2093
Schmickel RD
Waterson JR
P2860
P304
P356
10.1073/PNAS.75.11.5367
P407
P577
1978-11-01T00:00:00Z