Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 67

1.

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

Rondanino C, Duchesne V, Escalier D, Jumeau F, Verhaeghe F, Peers MC, Mitchell V, Rives N.

Reprod Biomed Online. 2015 Jul;31(1):89-99. doi: 10.1016/j.rbmo.2015.04.002. Epub 2015 Apr 16.

PMID:
26001636
2.

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

Mitchell V, Sigala J, Ballot C, Jumeau F, Barbotin AL, Duhamel A, Rives N, Rigot JM, Escalier D, Peers MC.

Andrologia. 2015 Mar;47(2):214-20. doi: 10.1111/and.12249. Epub 2014 Feb 24.

PMID:
24611953
3.

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

Ben Khelifa M, Coutton C, Zouari R, Karaouzène T, Rendu J, Bidart M, Yassine S, Pierre V, Delaroche J, Hennebicq S, Grunwald D, Escalier D, Pernet-Gallay K, Jouk PS, Thierry-Mieg N, Touré A, Arnoult C, Ray PF.

Am J Hum Genet. 2014 Jan 2;94(1):95-104. doi: 10.1016/j.ajhg.2013.11.017. Epub 2013 Dec 19.

4.

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

Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C, Tuffery P, Wolf JP, Becq F, Ray PF, Dulioust E, Gacon G, Bienvenu T, Touré A.

Am J Hum Genet. 2013 May 2;92(5):760-6. doi: 10.1016/j.ajhg.2013.03.016. Epub 2013 Apr 11.

5.

[ICSI treatment in severe asthenozoospermia].

Mitchell V, Sigala J, Jumeau F, Ballot C, Peers MC, Decanter C, Rives N, Perdrix A, Rigot JM, Escalier D.

Gynecol Obstet Fertil. 2012 Dec;40(12):776-9. doi: 10.1016/j.gyobfe.2012.10.003. Epub 2012 Nov 20. Review. French.

PMID:
23182233
6.

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

Kott E, Duquesnoy P, Copin B, Legendre M, Dastot-Le Moal F, Montantin G, Jeanson L, Tamalet A, Papon JF, Siffroi JP, Rives N, Mitchell V, de Blic J, Coste A, Clement A, Escalier D, Touré A, Escudier E, Amselem S.

Am J Hum Genet. 2012 Nov 2;91(5):958-64. doi: 10.1016/j.ajhg.2012.10.003.

7.

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

Blanchon S, Legendre M, Copin B, Duquesnoy P, Montantin G, Kott E, Dastot F, Jeanson L, Cachanado M, Rousseau A, Papon JF, Beydon N, Brouard J, Crestani B, Deschildre A, Désir J, Dollfus H, Leheup B, Tamalet A, Thumerelle C, Vojtek AM, Escalier D, Coste A, de Blic J, Clément A, Escudier E, Amselem S.

J Med Genet. 2012 Jun;49(6):410-6. doi: 10.1136/jmedgenet-2012-100867.

PMID:
22693285
8.

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

Escalier D, Touré A.

Med Sci (Paris). 2012 May;28(5):503-11. doi: 10.1051/medsci/2012285015. Epub 2012 May 30. Review. French.

9.

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

Coutton C, Zouari R, Abada F, Ben Khelifa M, Merdassi G, Triki C, Escalier D, Hesters L, Mitchell V, Levy R, Sermondade N, Boitrelle F, Vialard F, Satre V, Hennebicq S, Jouk PS, Arnoult C, Lunardi J, Ray PF.

Hum Reprod. 2012 Aug;27(8):2549-58. doi: 10.1093/humrep/des160. Epub 2012 May 24.

PMID:
22627659
10.

Septins at the annulus of mammalian sperm.

Toure A, Rode B, Hunnicutt GR, Escalier D, Gacon G.

Biol Chem. 2011 Aug;392(8-9):799-803. doi: 10.1515/BC.2011.074. Epub 2011 Jul 11. Review.

PMID:
21740329
11.

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

Merveille AC, Davis EE, Becker-Heck A, Legendre M, Amirav I, Bataille G, Belmont J, Beydon N, Billen F, Clément A, Clercx C, Coste A, Crosbie R, de Blic J, Deleuze S, Duquesnoy P, Escalier D, Escudier E, Fliegauf M, Horvath J, Hill K, Jorissen M, Just J, Kispert A, Lathrop M, Loges NT, Marthin JK, Momozawa Y, Montantin G, Nielsen KG, Olbrich H, Papon JF, Rayet I, Roger G, Schmidts M, Tenreiro H, Towbin JA, Zelenika D, Zentgraf H, Georges M, Lequarré AS, Katsanis N, Omran H, Amselem S.

Nat Genet. 2011 Jan;43(1):72-8. doi: 10.1038/ng.726. Epub 2010 Dec 5.

12.

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

Perdrix A, Travers A, Chelli MH, Escalier D, Do Rego JL, Milazzo JP, Mousset-Siméon N, Macé B, Rives N.

Hum Reprod. 2011 Jan;26(1):47-58. doi: 10.1093/humrep/deq297. Epub 2010 Nov 18.

PMID:
21088015
13.

[Human asthenozoospermia and structural defects of the annulus].

Lhuillier P, Escalier D, Gacon G, Dulioust E, Touré A.

Med Sci (Paris). 2010 Aug-Sep;26(8-9):688-9. doi: 10.1051/medsci/2010268-9688. French. No abstract available.

14.

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

Duquesnoy P, Escudier E, Vincensini L, Freshour J, Bridoux AM, Coste A, Deschildre A, de Blic J, Legendre M, Montantin G, Tenreiro H, Vojtek AM, Loussert C, Clément A, Escalier D, Bastin P, Mitchell DR, Amselem S.

Am J Hum Genet. 2009 Dec;85(6):890-6. doi: 10.1016/j.ajhg.2009.11.008.

15.

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

Bai X, Silvius D, Chan ED, Escalier D, Xu SX.

Nucleic Acids Res. 2009 May;37(8):2699-711. doi: 10.1093/nar/gkp094. Epub 2009 Mar 9.

16.

Absence of annulus in human asthenozoospermia: case report.

Lhuillier P, Rode B, Escalier D, Lorès P, Dirami T, Bienvenu T, Gacon G, Dulioust E, Touré A.

Hum Reprod. 2009 Jun;24(6):1296-303. doi: 10.1093/humrep/dep020. Epub 2009 Feb 15.

PMID:
19221096
17.

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

Dieterich K, Zouari R, Harbuz R, Vialard F, Martinez D, Bellayou H, Prisant N, Zoghmar A, Guichaoua MR, Koscinski I, Kharouf M, Noruzinia M, Nadifi S, Sefiani A, Lornage J, Zahi M, Viville S, Sèle B, Jouk PS, Jacob MC, Escalier D, Nikas Y, Hennebicq S, Lunardi J, Ray PF.

Hum Mol Genet. 2009 Apr 1;18(7):1301-9. doi: 10.1093/hmg/ddp029. Epub 2009 Jan 15.

PMID:
19147683
18.

[Knockout mice in the service of reproduction].

Escalier D.

Gynecol Obstet Fertil. 2008 Dec;36(12):1224-9. doi: 10.1016/j.gyobfe.2008.10.005. Epub 2008 Nov 12. Review. French.

PMID:
19008143
19.

[An anion transporter is essential for spermatozoa motility].

Lhuillier P, Escalier D, Gacon G, Touré A.

Med Sci (Paris). 2008 Mar;24(3):226-8. doi: 10.1051/medsci/2008243226. French. No abstract available.

20.

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

Touré A, Lhuillier P, Gossen JA, Kuil CW, Lhôte D, Jégou B, Escalier D, Gacon G.

Hum Mol Genet. 2007 Aug 1;16(15):1783-93. Epub 2007 May 20.

PMID:
17517695
21.

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

Duriez B, Duquesnoy P, Escudier E, Bridoux AM, Escalier D, Rayet I, Marcos E, Vojtek AM, Bercher JF, Amselem S.

Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3336-41. Epub 2007 Feb 20. Erratum in: Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6490.

22.

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

Prisant N, Escalier D, Soufir JC, Morillon M, Schoevaert D, Misrahi M, Tachdjian G.

Hum Reprod. 2007 Apr;22(4):1052-9. Epub 2007 Jan 5.

PMID:
17208942
23.

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

Ravel C, Chantot-Bastaraud S, Siffroi JP, Escalier D, Antoine JM, Mandelbaum J.

Fertil Steril. 2006 Sep;86(3):719.e1-7.

PMID:
16952512
24.

[Animal models: Candidate genes for human male infertility].

Escalier D.

Gynecol Obstet Fertil. 2006 Sep;34(9):827-30. Epub 2006 Aug 23. Review. French.

PMID:
16931095
25.

New fibrous sheath anomaly in spermatozoa of men with consanguinity.

Escalier D, Albert M.

Fertil Steril. 2006 Jul;86(1):219.e1-9. Epub 2006 Jun 5.

PMID:
16750828
26.

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

Mitchell V, Rives N, Albert M, Peers MC, Selva J, Clavier B, Escudier E, Escalier D.

Hum Reprod. 2006 Aug;21(8):2065-74. Epub 2006 Apr 27.

PMID:
16644911
27.

Knockout mouse models of sperm flagellum anomalies.

Escalier D.

Hum Reprod Update. 2006 Jul-Aug;12(4):449-61. Epub 2006 Mar 24. Review.

PMID:
16565154
28.
29.

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

Escalier D, Garchon HJ.

Mol Reprod Dev. 2005 Sep;72(1):105-12.

PMID:
15818601
30.

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

Segretain D, Decrouy X, Dompierre J, Escalier D, Rahman N, Fiorini C, Mograbi B, Siffroi JP, Huhtaniemi I, Fenichel P, Pointis G.

Mol Carcinog. 2003 Dec;38(4):179-87.

PMID:
14639657
31.
32.

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

Escalier D, Bai XY, Silvius D, Xu PX, Xu X.

Mol Reprod Dev. 2003 Jul;65(3):298-308.

PMID:
12784252
33.

New insights into the assembly of the periaxonemal structures in mammalian spermatozoa.

Escalier D.

Biol Reprod. 2003 Aug;69(2):373-8. Epub 2003 Apr 2. Review.

PMID:
12672659
34.

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

Naud N, Touré A, Liu J, Pineau C, Morin L, Dorseuil O, Escalier D, Chardin P, Gacon G.

Biochem J. 2003 May 15;372(Pt 1):105-12.

36.
37.

Impact of genetic engineering on the understanding of spermatogenesis.

Escalier D.

Hum Reprod Update. 2001 Mar-Apr;7(2):191-210. Review.

PMID:
11284662
38.
39.

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

Escalier D.

Histol Histopathol. 1999 Jul;14(3):959-71. doi: 10.14670/HH-14.959. Review.

PMID:
10425564
40.

Mammalian spermatogenesis investigated by genetic engineering.

Escalier D.

Histol Histopathol. 1999 Jul;14(3):945-58. doi: 10.14670/HH-14.945. Review.

PMID:
10425563
41.
42.

A 21-kDa polypeptide belonging to a new family of proteins is expressed in the Golgi apparatus of neural and germ cells.

Sabéran-Djoneidi D, Picart R, Escalier D, Gelman M, Barret A, Tougard C, Glowinski J, Lévi-Strauss M.

J Biol Chem. 1998 Feb 13;273(7):3909-14.

43.
44.

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

Allenet B, Escalier D, Garchon HJ.

Mamm Genome. 1995 Sep;6(9):640-4.

PMID:
8535073
45.

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

Bermúdez D, Escalier D, Gallo JM, Viellefond A, Ríus F, Pérez de Vargas I, Schrével J.

J Reprod Fertil. 1994 Mar;100(2):567-75.

PMID:
8021878
46.

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

Calenda A, Allenet B, Escalier D, Bach JF, Garchon HJ.

EMBO J. 1994 Jan 1;13(1):100-9.

47.

Pregnancy after subzonal insemination with spermatozoa lacking outer dynein arms.

Wolf JP, Feneux D, Escalier D, Rodrigues D, Frydman R, Jouannet P.

J Reprod Fertil. 1993 Mar;97(2):487-92.

PMID:
8501720
48.

[A new entity of sperm pathology: peri-axonemal flagellar dyskinesia].

David G, Feneux D, Serres C, Escalier D, Jouannet P.

Bull Acad Natl Med. 1993 Feb;177(2):263-71; discussion 272-5. French.

PMID:
8353778
49.

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

Escalier D, Bermùdez D, Gallo JM, Viellefond A, Schrével J.

Differentiation. 1992 Nov;51(3):233-43.

PMID:
1459363
50.

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

Albert M, Gallo JM, Escalier D, Parseghian N, Jouannet P, Schrevel J, David G.

Hum Reprod. 1992 Oct;7(9):1249-56.

PMID:
1479007

Supplemental Content

Loading ...
Support Center