A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population (Q89477973)

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scientific article published on 10 July 2018

Language	Label	Description	Also known as
English	A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population	scientific article published on 10 July 2018

Statements

scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

cystic fibrosis

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based on heuristic

inferred from title

congenital bilateral aplasia of the vas deferens

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based on heuristic

inferred from title

Reza Mirfakhraie

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

author name string

Fatemeh Asadi

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

Farzaneh Mirzajani

3

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5 April 2020

publication date

10 July 2018

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

Iranian biomedical journal

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

23

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5 April 2020

2

1 reference

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PMC publication ID

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5 April 2020

92-98

1 reference

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PMC publication ID

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5 April 2020

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the azoospermic patient.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis mutation screening in healthy men with reduced sperm quality

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzyme digestion

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards an understanding of the genetics of human male infertility: lessons from flies

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis by mass spectrometry of 100 cystic fibrosis gene mutations in 92 patients with congenital bilateral absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse models of male infertility.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic dissection of mammalian fertility pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis transmembrane conductance regulator gene screening and clinical correlation in Taiwanese males with congenital bilateral absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Causes of azoospermia and their management

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathology of the CFTR locus in male infertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia]

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective CFTR-dependent CREB activation results in impaired spermatogenesis and azoospermia

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of Two Neighboring CFTR Mutations in Iranian Infertile Men with Non-Obstructive Azoospermia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/29986553

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29986553%20AND%20SRC:MED&resulttype=core&format=json

5 April 2020

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