The genetics of male infertility in relation to cystic fibrosis (Q47736600)

5 February 2018

review article

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title

The genetics of male infertility in relation to cystic fibrosis (English)

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5 February 2018

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1

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5 February 2018

author name string

Liebaers I

series ordinal

2

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5 February 2018

publication date

1 December 1997

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5 February 2018

Bailliere's clinical obstetrics and gynaecology

published in

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5 February 2018

volume

11

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5 February 2018

issue

4

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5 February 2018

page(s)

797-817

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5 February 2018

Severity of chest disease in cystic fibrosis patients in relation to their genotypes

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Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect

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Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected

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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

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Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA

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Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens

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Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations

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Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels

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7 January 2021

Etiologic factors in 1294 consecutive cases of male infertility

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Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens

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Abnormal distribution of cystic fibrosis delta F508 allele in adults with chronic bronchial hypersecretion

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Congenital bilateral absence of vas deferens in absence of cystic fibrosis

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Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

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Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens

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Detection of over 98% cystic fibrosis mutations in a Celtic population

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Screening Young syndrome patients for CFTR mutations

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A Cystic Fibrosis Mutation Associated with Mild Lung Disease

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Sweat chloride and delta F508 mutation in chronic bronchitis or bronchiectasis

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Vasa aplasia and cystic fibrosis

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The ABC of channel regulation

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A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

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Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

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7 January 2021

Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia

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7 January 2021

Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation

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7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

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The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

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A mutation in CFTR produces different phenotypes depending on chromosomal background

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Congenital unilateral absence of the vas deferens: a heterogeneous disorder with two distinct subpopulations based upon aetiology and mutational status of the cystic fibrosis gene

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Uniparental inheritance of microsatellite alleles of the cystic fibrosis gene (CFTR): identification of a 50 kilobase deletion

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7 January 2021

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7 January 2021

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Congenital absence of the vas deferens: a mild form of cystic fibrosis

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7 January 2021

Aetiology of congenital absence of vas deferens: genetic study of three generations

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7 January 2021

Cystic fibrosis mutations impair the fertilization rate of epididymal sperm from men with congenital absence of the vas deferens.

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7 January 2021

Two births after microsurgical sperm aspiration in congenital absence of vas deferens

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7 January 2021

Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

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7 January 2021

Cystic fibrosis and congenital absence of the vas deferens

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7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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7 January 2021

Identification of the cystic fibrosis gene: chromosome walking and jumping

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7 January 2021

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

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7 January 2021

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7 January 2021

Cystic fibrosis gene mutations do not affect sperm function during in vitro fertilization with micromanipulation for men with bilateral congenital absence of vas deferens.

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7 January 2021

New treatment for infertility due to congenital absence of vas deferens

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7 January 2021

Pregnancy with sperm aspiration from the proximal head of the epididymis: A new treatment for congenital absence of the vas deferens

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7 January 2021

Congenital absence of the vas deferens. The fertilizing capacity of human epididymal sperm

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7 January 2021

Conventional in-vitro fertilization versus intracytoplasmic sperm injection for patients requiring microsurgical sperm aspiration.

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7 January 2021

The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: the genetic implications for male infertility

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7 January 2021

Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts

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7 January 2021

High fertilization and implantation rates after intracytoplasmic sperm injection.

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7 January 2021

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels

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7 January 2021

Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.

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7 January 2021

Microsurgical epididymal sperm aspiration and intracytoplasmic sperm injection: a new effective approach to infertility as a result of congenital bilateral absence of the vas deferens.

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7 January 2021

Cystic fibrosis mutation screening in healthy men with reduced sperm quality

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7 January 2021

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

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7 January 2021

Universal community carrier screening for cystic fibrosis?

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7 January 2021

Cystic fibrosis: genotypic and phenotypic variations

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7 January 2021

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

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7 January 2021

10.1016/S0950-3552(97)80014-4

Identifiers

DOI

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5 February 2018

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5 February 2018