Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I.

P2860

Q37120427-2C686ADA-BC70-43F4-9F5F-DB1835BA678F

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Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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http://www.wikidata.org/entity/Q34989078

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2013 nî lūn-bûn

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2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Marked repression of CFTR mRNA in the transgenic Cftr

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Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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type

Item

label

Marked repression of CFTR mRNA in the transgenic Cftr

@nl

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

@ast

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

@en

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Marked repression of CFTR mRNA in the transgenic Cftr

@nl

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

@ast

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

@en

P1476

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

@en

P2093

Bradford A Woodworth

http://www.w3.org/2001/XMLSchema#string

Daniel Skinner

http://www.w3.org/2001/XMLSchema#string

David M Bedwell

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Eric J Sorscher

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Jessica A Buckley-Lanier

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Neel K Ranganath

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Shaoyan Zhang

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P2860

Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain.

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A mouse model for the delta F508 allele of cystic fibrosis.

In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium

Chimeric constructs endow the human CFTR Cl- channel with the gating behavior of murine CFTR

Comparison of cystic fibrosis transmembrane conductance regulator (CFTR) and ciliary beat frequency activation by the CFTR Modulators Genistein, VRT-532, and UCCF-152 in primary sinonasal epithelial cultures.

A mouse model for the cystic fibrosis delta F508 mutation.

Comparison of vectorial ion transport in primary murine airway and human sinonasal air-liquid interface cultures, models for studies of cystic fibrosis, and other airway diseases.

Generation and characterization of a delta F508 cystic fibrosis mouse model.

P304

351-352

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P31

scholarly article

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10.1016/J.JCF.2013.11.009

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2013-12-27T00:00:00Z

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259498668

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24378376

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P932

4300118

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Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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P2860

P2860

Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932