D. Escalier

发表

Failure of differentiation of the nuclear-perinuclear skeletal complex in the round-headed human spermatozoa.

D. Escalier, 1990, The International journal of developmental biology.

Knockout mouse models of sperm flagellum anomalies.

D. Escalier, 2006, Human reproduction update.

Outcome of ICSI with ejaculated spermatozoa in a series of men with distinct ultrastructural flagellar abnormalities.

D. Escalier, E. Escudier, N. Rives, 2006, Human reproduction.

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.

P. Jouk, F. Abada, P. Ray, 2012, Human reproduction.

Assessment of acrosome and nuclear abnormalities in human spermatozoa with large vacuoles.

J. Milazzo, A. Travers, M. Chelli, 2011, Human reproduction.

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

A. Rousseau, S. Amselem, H. Dollfus, 2012, Journal of Medical Genetics.

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

A. Rousseau, S. Amselem, A. Clément, 2012, Journal of Medical Genetics.

Human spermatozoa with large heads and multiple flagella: a quantitative ultrastructural study of 6 cases

D. Escalier, 1983, Biology of the cell.

Ultrastructural nuclear defects and increased chromosome aneuploidies in spermatozoa with elongated heads.

G. Tachdjian, D. Escalier, D. Schoevaert, 2007, Human reproduction.

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.

Light microscopy morphological characteristics of the sperm flagellum may be related to axonemal abnormalities

D. Escalier, F. Jumeau, J. Rigot, 2015, Andrologia.

Impact of genetic engineering on the understanding of spermatogenesis.

D. Escalier, D. Escalier, 2001, Human reproduction update.

Sex-Specific Gene Expression During Meiotic Prophase I: Xlr (X Linked, Lymphocyte Regulated), Not Its Male Homologue Xmr (Xlr Related, Meiosis Regulated), Is Expressed in Mouse Oocytes

H. Garchon, D. Escalier, L. Eloy, 2002, Biology of reproduction.

Mammalian spermatogenesis investigated by genetic engineering.

D. Escalier, 1999, Histology and histopathology.

Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia.

S. Amselem, A. Clément, B. Copin, 2012, American journal of human genetics.

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

J. Belmont, H. Zentgraf, J. Towbin, 2011, Nature Genetics.

Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia.

S. Amselem, A. Clément, D. Escalier, 2009, American journal of human genetics.

New Insights into the Assembly of the Periaxonemal Structures in Mammalian Spermatozoa

D. Escalier, 2003, Biology of reproduction.

Spermatid nuclear and sperm periaxonemal anomalies in the mouse Ube2b null mutant

D. Escalier, X. Bai, P. Xu, 2003, Molecular reproduction and development.

The cytoplasmic matrix of the human spermatozoon: cross‐filaments link the various cell components

D. Escalier, 1984, Biology of the cell.

Spermatogenesis of mice lacking CK2α′: Failure of germ cell survival and characteristic modifications of the spermatid nucleus

D. Escalier, Derek Silvius, Xin Xu, 2003, Molecular reproduction and development.

XMR is associated with the asynapsed segments of sex chromosomes in the XY body of mouse primary spermatocytes

H. Garchon, D. Escalier, 2000, Chromosoma.

J. Bernaudin, D. Escalier, E. Escudier, 1990, The American review of respiratory disease.

Genetic approach to male meiotic division deficiency: the human macronuclear spermatozoa.

D. Escalier, 2002, Molecular human reproduction.

Cytoplasmic events in human meiotic arrest as revealed by immunolabelling of spermatocyte proacrosin.

J. Gallo, D. Escalier, A. Viellefond, 1992, Differentiation; research in biological diversity.

The meiosis‐specific Xmr gene product is homologous to the lymphocyte Xlr protein and is a component of the XY body.

H. Garchon, A. Calenda, D. Escalier, 1994, The EMBO journal.

High level expression of the Xlr nuclear protein in immature thymocytes and colocalization with the matrix-associated region-binding SATB1 protein.

H. Garchon, D. Escalier, A. Badrichani, 1999, Journal of immunology.

XMR, a dual location protein in the XY pair and in its associated nucleolus in mouse spermatocytes

H. Garchon, D. Escalier, 2005, Molecular reproduction and development.

A putative human equivalent of the murine Xlr (X-linked, lymphocyte-regulated) protein

H. Garchon, D. Escalier, B. Allenet, 1995, Mammalian Genome.

Evaluation of sperm nuclear integrity in patients with different percentages of decapitated sperm in ejaculates.

D. Escalier, F. Jumeau, N. Rives, 2015, Reproductive biomedicine online.

Proacrosin as a marker of meiotic and post-meiotic germ cell differentiation: quantitative assessment of human spermatogenesis with a monoclonal antibody.

F Ríus, J. Gallo, D. Escalier, 1994, Journal of reproduction and fertility.

Unexplained in-vitro fertilization failure: implication of acrosomes with a small reacting region, as revealed by a monoclonal antibody.

P. Jouannet, J. Gallo, D. Escalier, 1992, Human reproduction.

What are the germ cell phenotypes from infertile men telling us about spermatogenesis?

D. Escalier, 1999, Histology and histopathology.

evaluation. Characterization of a monoclonal antibody to human proacrosin and its use in acrosomal status

J. Gallo, D. Escalier, P. Grellier, 2011 .

Characterization of a monoclonal antibody to human proacrosin and its use in acrosomal status evaluation.

J. Gallo, D. Escalier, P. Grellier, 1991, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[ICSI treatment in severe asthenozoospermia].

D. Escalier, F. Jumeau, J. Rigot, 2012, Gynecologie, obstetrique & fertilite.

Tail stump syndrome associated with chromosomal translocation in two brothers attempting intracytoplasmic sperm injection.

C. Ravel, S. Chantot-Bastaraud, J. Antoine, 2006, Fertility and sterility.

Facilitation reaction (enhancing antibodies and suppressor cells) and rejection reaction (sensitized cells) from the mother to the paternal antigens of the conceptus.

D. Escalier, G. Chaouat, G. Voisin, 1979, Clinical and experimental immunology.

Human acrosome biogenesis: immunodetection of proacrosin in primary spermatocytes and of its partitioning pattern during meiosis.

J. Gallo, D. Escalier, M. Albert, 1991, Development.

Absence of annulus in human asthenozoospermia: case report.

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

New fibrous sheath anomaly in spermatozoa of men with consanguinity.

D. Escalier, M. Albert, 2006, Fertility and sterility.

Septins at the annulus of mammalian sperm

G. Hunnicutt, D. Escalier, A. Touré, 2011, Biological chemistry.

Arrest of flagellum morphogenesis with fibrous sheath immaturity of human spermatozoa

D. Escalier, 2006, Andrologia.

Impaired ability of human spermatozoa to penetrate zona-free hamster oocytes: is a postacrosomal sheath anomaly involved?

P. Jouannet, D. Escalier, G. David, 1987, Gamete research.

A 21-kDa Polypeptide Belonging to a New Family of Proteins Is Expressed in the Golgi Apparatus of Neural and Germ Cells*

J. Glowinski, R. Picart, D. Sabéran-Djoneidi, 1998, The Journal of Biological Chemistry.

The testis anion transporter 1 (Slc26a8) is required for sperm terminal differentiation and male fertility in the mouse.

B. Jégou, D. Escalier, A. Touré, 2007, Human molecular genetics.

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

N. Thierry-Mieg, D. Grunwald, P. Jouk, 2014, American journal of human genetics.

Pathology of the cytoskeleton of the human sperm flagellum: axonemal and peri‐axonemal anomalies

D. Escalier, G. David, 1984, Biology of the cell.

A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia

S. Amselem, J. Bercher, D. Escalier, 2007, Proceedings of the National Academy of Sciences.

Reproductive genetics MLPA and sequence analysis of DPY 19 L 2 reveals point mutations causing globozoospermia

P. Jouk, F. Abada, P. Ray, 2012 .

Rho family GTPase Rnd2 interacts and co-localizes with MgcRacGAP in male germ cells.

C. Pineau, N. Naud, Jianfeng Liu, 2003, The Biochemical journal.

Actin in spermatids and spermatozoa of Teladorsagia circumcincta and Trichostrongylus colubriformis (Nematoda, Trichostrongylida)

J. Justine, D. Escalier, J. Cabaret, 1997 .

Identification and characterization of a novel testis-specific gene CKT2, which encodes a substrate for protein kinase CK2

E. Chan, D. Escalier, X. Bai, 2009, Nucleic acids research.

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.

P. Jouk, S. Viville, P. Ray, 2009, Human molecular genetics.

[Morphological defects of sperm flagellum implicated in human male infertility].

D. Escalier, A. Touré, 2012, Medecine sciences : M/S.

Ultrastructural morphometry of the human sperm flagellum with a stereological analysis of the lengths of the dense fibres

D. Escalier, C. Serres, G. David, 1983, Biology of the cell.

Quantitative Ultrastructural Modifications in Human Spermatozoa after Freezing

D. Escalier, J. Bisson, 1980 .

[Knockout mice in the service of reproduction].

D. Escalier, 2008, Gynecologie, obstetrique & fertilite.

Sequestration of connexin43 in the early endosomes: An early event of Leydig cell tumor progression

I. Huhtaniemi, C. Fiorini, B. Mograbi, 2003, Molecular carcinogenesis.

Unexpectedly normal cilia and spermatozoa in an infertile man with Kartagener's syndrome.

J. Bernaudin, D. Escalier, E. Escudier, 1987, European journal of respiratory diseases.

Is there a relationship between large vacuoles in spermatozoa and nucleus or acrosome alterations

J. Milazzo, A. Travers, D. Escalier, 2010 .

Immunochemical Characterization of a Human Sperm Fibrous Sheath Protein, Its Developmental Expression Pattern, and Morphogenetic Relationships with Actin

J. Gallo, D. Escalier, J. Schrével, 1997, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.