E. Dulioust

发表

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

P. Tufféry, P. Ray, T. Dirami, 2013, American journal of human genetics.

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018, American journal of human genetics.

Detection and quantification of HIV-1 in semen: identification of a subpopulation of men at high potential risk of viral sexual transmission.

C. Rouzioux, P. Jouannet, E. Dulioust, 1999, AIDS.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

No detection of HIV 1-RNA in semen of men on efficient HAART in the past 4 years of a 2002–2009 survey

C. Rouzioux, P. Jouannet, P. Sogni, 2010, AIDS.

Decreased ovarian reserve in HIV-infected women

P. Santulli, L. Marcellin, C. Chapron, 2016, AIDS.

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.

M. Ikawa, P. Ray, L. Jin, 2020, American journal of human genetics.

Assisted reproduction in HIV-1-serodifferent couples: the need for viral validation of processed semen

C. Rouzioux, L. Mandelbrot, P. Jouannet, 2002, AIDS.

Semen alterations in HIV-1 infected men.

C. Rouzioux, D. Costagliola, L. Mandelbrot, 2002, Human reproduction.

IgG subclass distribution in serum and various mucosal fluids of HIV type 1-infected subjects.

J. Excler, E. Dulioust, D. Salmon-Céron, 2000, AIDS research and human retroviruses.

Impaired sperm motility in HIV-infected men: an unexpected adverse effect of efavirenz?

S. Grabar, P. Jouannet, P. Sogni, 2015, Human reproduction.

Development and validation of a LC-MS/MS method for the quantification of tenofovir and emtricitabine in seminal plasma.

J. Wolf, E. Dulioust, J. Treluyer, 2016, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Cyclophosphamide in the male rat: cerebral biochemical changes in progeny.

E. Dulioust, E. Kempf, M. Auroux, 1990, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Hepatitis C virus in the semen of men coinfected with HIV-1: prevalence and origin

C. Rouzioux, S. Pol, P. Jouannet, 2005, AIDS.

Detection of HIV-1 in seminal plasma and seminal cells of HIV-1 seropositive men.

C. Rouzioux, P. Jouannet, E. Dulioust, 1998, Journal of reproductive immunology.

Antimitotic drugs (cyclophosphamide and vinblastine) in the male rat. Deaths and behavioral abnormalities in the offspring.

E. Dulioust, M. Auroux, N. Nawar, 1986, Journal of andrology.

Diagnostic genetic screening for assisted reproductive technologies patients with macrozoospermia

J. Auger, J. Dupont, E. Dulioust, 2017, Andrology.

Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.

N. Thierry-Mieg, B. Conne, P. Ray, 2019, American journal of human genetics.

Absence of annulus in human asthenozoospermia: case report.

T. Dirami, T. Bienvenu, D. Escalier, 2009, Human reproduction.

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.

P. Ray, S. Savinov, F. Guillonneau, 2019, American journal of human genetics.

Homozygous 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

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

Comparison of the distribution of IgG and IgA antibodies in serum and various mucosal fluids of HIV type 1-infected subjects.

J. Excler, E. Dulioust, D. Salmon-Céron, 1999, AIDS research and human retroviruses.

Development and standardization of methods to evaluate the antibody response to an HIV-1 candidate vaccine in secretions and sera of seronegative vaccine recipients.

J. Excler, E. Dulioust, D. Salmon-Céron, 1999, Journal of immunological methods.

Zika virus and reproduction: facts, questions and current management

A. Benachi, L. Epelboin, C. Patrat, 2017, Human reproduction update.

HIV-positive patients undertaking ART have longer infertility histories than age-matched control subjects.

P. Santulli, C. Chapron, N. Chopin, 2011, Fertility and sterility.

Assisted reproductive technology outcomes in women with a chronic viral disease

P. Santulli, L. Marcellin, C. Chapron, 2021, AIDS.

Decreased ovarian reserve in human immunodeficiency virus infected women: A matched cohort study.

P. Santulli, L. Marcellin, C. Chapron, 2016, AIDS.

Testicular impairment in Primary Adrenal Insufficiency caused by Nicotinamide Nucleotide Transhydrogenase (NNT) deficiency - a case report: implication of oxidative stress and importance of fertility preservation

X. Bertagna, C. Patrat, E. Dulioust, 2023, Basic and Clinical Andrology.

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility

N. Thierry-Mieg, P. Santulli, P. Ray, 2021, Clinical genetics.

Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia

T. Dirami, A. Touré, G. Gacon, 2015, Basic and Clinical Andrology.

Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility

N. Thierry-Mieg, P. Ray, Y. Fichou, 2020, Journal of Medical Genetics.

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

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2021, Human Genetics.

Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.

P. Santulli, A. Schmitt, A. Touré, 2021, Human reproduction.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Corrigendum: Homozygous 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.

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Intracytoplasmic sperm injection with microsurgically retrieved spermatozoa in azoospermic men infected with human immunodeficiency virus 1 or hepatitis C virus: the EP43 AZONECO ANRS study.

S. Grabar, P. Sogni, O. Launay, 2013, Fertility and sterility.

Decrease in HIV-1 seminal shedding in men receiving highly active antiretroviral therapy: an 18 month longitudinal study (ANRS EP012).

C. Rouzioux, P. Jouannet, B. Silbermann, 2002, AIDS.

Penetration and antiviral efficacy of total and unbound maraviroc, raltegravir and rilpivirine in both female and male genital fluids from HIV-positive patients receiving regimens containing these antiretrovirals

M. Lê, G. Peytavin, O. Launay, 2017, The Journal of antimicrobial chemotherapy.

Absence of CFAP 69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018 .

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans

N. Thierry-Mieg, P. Ray, Caroline Cazin, 2023, iScience.

Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.

N. Thierry-Mieg, P. Ray, E. Bieth, 2023, Journal of genetics and genomics = Yi chuan xue bao.

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.

CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.

P. Ray, Caroline Cazin, A. Touré, 2023, Clinical Genetics.