Tissue-specific in vivo transcription start sites of the human and murine cystic fibrosis genes.

No abstract is available for this paper.

• Publication year

  1998

• Venue

  Human Molecular Genetics

• Publication date

  1998-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/HMG/7.3.363PMID 9466991
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1997cited by this paper
• Translational control in spermatogenesis.

  1995cited by this paper
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  1995cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1992cited by this paper
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  1992cited by this paper
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  1992cited by this paper
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  1992cited by this paper
• Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR).

  1992cited by this paper
• Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

  1991influential reference
• Structural features in eukaryotic mRNAs that modulate the initiation of translation.

  1991cited by this paper
• The cystic fibrosis gene has a "housekeeping"-type promoter and is expressed at low levels in cells of epithelial origin.

  1991cited by this paper
• Characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene.

  1991cited by this paper
• Immunocytochemical localization of the cystic fibrosis gene product CFTR.

  1991cited by this paper
• In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator

  1991cited by this paper
• An analysis of vertebrate mRNA sequences: intimations of translational control

  1991cited by this paper
• Post-meiotic gene expression.

  1990cited by this paper
• Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA

  1989cited by this paper
• Identification of the cystic fibrosis gene: chromosome walking and jumping.

  1989cited by this paper
• Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

  1989cited by this paper
• The Metabolic basis of inherited disease

  1989cited by this paper
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  1988cited by this paper
• Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

  1987cited by this paper
• A catalogue of splice junction sequences.

  1982cited by this paper
• The metabolic basis of inherited disease

  1961cited by this paper

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  2015cites this paper
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  2015cites this paper
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  2015cites this paper
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  2015cites this paper
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  2014cites this paper
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  2013cites this paper
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  2013cites this paper
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  2013cites this paper
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  2011cites this paper
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  2009cites this paper
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  2008influential citation
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  2007cites this paper
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  2007cites this paper
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  2006cites this paper
• [Cystic fibrosis: molecular update and clinical implications].

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  1999cites this paper
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  1999cites this paper
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  1999cites this paper
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