Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manif
about
The unfolded protein response affects readthrough of premature termination codonsTrans-splicing into highly abundant albumin transcripts for production of therapeutic proteins in vivo.Gene transfer for cystic fibrosisA shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia.Airway epithelial CFTR mRNA expression in cystic fibrosis patients after repetitive administration of a recombinant adenovirus.Gene transfer into respiratory epithelial cells by targeting the polymeric immunoglobulin receptor.Association of cystic fibrosis transmembrane conductance regulator gene variants with acute lung injury in African American children with pneumonia*.In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glandsCurrent status of gene therapy for inherited lung diseasesThe ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs.Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis.Macromolecular interactions and ion transport in cystic fibrosis.The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurementsAtypical 5' splice sites cause CFTR exon 9 to be vulnerable to skipping.Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis.Cell therapy for cystic fibrosis.Cystic fibrosis genetics: from molecular understanding to clinical application.Repairing the basic defect in cystic fibrosis - one approach is not enough.Impact of gene editing on the study of cystic fibrosis.Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides.Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct Cl- transport and overexpression can generate basolateral CFTR.Ectopic (illegitimate) transcription: new possibilities for the analysis and diagnosis of human genetic disease.Structural diversity in the 5'-untranslated region of cytokine-stimulated human inducible nitric oxide synthase mRNA.Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.Nominal carbonic anhydrase activity minimizes airway-surface liquid pH changes during breathing.Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.Markers of Cell Proliferation and Expression of Melanosomal Antigen in Lymphangioleiomyomatosis
P2860
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P2860
Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manif
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Extensive posttranscriptional ...... ciated with the clinical manif
@ast
Extensive posttranscriptional ...... ciated with the clinical manif
@en
type
label
Extensive posttranscriptional ...... ciated with the clinical manif
@ast
Extensive posttranscriptional ...... ciated with the clinical manif
@en
prefLabel
Extensive posttranscriptional ...... ciated with the clinical manif
@ast
Extensive posttranscriptional ...... ciated with the clinical manif
@en
P2093
P2860
P356
P1476
Extensive posttranscriptional ...... ciated with the clinical manif
@en
P2093
Crystal RG
Curristin SM
Cutting GR
Trapnell BC
P2860
P304
P356
10.1172/JCI115952
P407
P577
1992-09-01T00:00:00Z