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Emmanuel Dulioust Selected Research

Asthenozoospermia

7/2021Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
7/2021A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
10/2020Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility.
12/2019Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
1/2018Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.
1/2015Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia.

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Emmanuel Dulioust Research Topics

Disease

6Asthenozoospermia
07/2021 - 01/2015
6Male Infertility (Male Sterility)
07/2021 - 01/2018
2Bardet-Biedl Syndrome (Syndrome, Bardet-Biedl)
07/2021 - 07/2021
2Ciliary Motility Disorders (Primary Ciliary Dyskinesia)
01/2019 - 01/2018
1Infections
11/2005
1Hepatitis C
11/2005

Drug/Important Bio-Agent (IBA)

4Proteins (Proteins, Gene)FDA Link
10/2020 - 01/2015
2TubulinIBA
07/2021 - 07/2021
2Adenylate KinaseIBA
01/2019 - 01/2018
1Calmodulin (Calcium-Dependent Activator Protein)IBA
10/2020
1RNA (Ribonucleic Acid)IBA
11/2005