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Year Number of Results
2003 2
2004 3
2005 3
2006 6
2007 3
2009 4
2010 2
2011 1
2012 2
2013 1
2015 2
2016 1
2017 4
2018 7
2020 3
2021 1
2022 3
2023 2
2024 2

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49 results

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Page 1
SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.
Bogaert E, Garde A, Gautier T, Rooney K, Duffourd Y, LeBlanc P, van Reempts E, Tran Mau-Them F, Wentzensen IM, Au KS, Richardson K, Northrup H, Gatinois V, Geneviève D, Louie RJ, Lyons MJ, Laulund LW, Brasch-Andersen C, Maxel Juul T, El It F, Marle N, Callier P, Relator R, Haghshenas S, McConkey H, Kerkhof J, Cesario C, Novelli A, Brunetti-Pierri N, Pinelli M, Pennamen P, Naudion S, Legendre M, Courdier C, Trimouille A, Fenzy MD, Pais L, Yeung A, Nugent K, Roeder ER, Mitani T, Posey JE, Calame D, Yonath H, Rosenfeld JA, Musante L, Faletra F, Montanari F, Sartor G, Vancini A, Seri M, Besmond C, Poirier K, Hubert L, Hemelsoet D, Munnich A, Lupski JR, Philippe C, Thauvin-Robinet C, Faivre L, Sadikovic B, Govin J, Dermaut B, Vitobello A. Bogaert E, et al. Among authors: govin j. Am J Hum Genet. 2023 May 4;110(5):790-808. doi: 10.1016/j.ajhg.2023.03.016. Epub 2023 Apr 17. Am J Hum Genet. 2023. PMID: 37071997 Free PMC article.
Genome reprogramming during sporulation.
Govin J, Berger SL. Govin J, et al. Int J Dev Biol. 2009;53(2-3):425-32. doi: 10.1387/ijdb.082687jg. Int J Dev Biol. 2009. PMID: 19412896 Free PMC article. Review.
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.
Cavarocchi E, Sayou C, Lorès P, Cazin C, Stouvenel L, El Khouri E, Coutton C, Kherraf ZE, Patrat C, Govin J, Thierry-Mieg N, Whitfield M, Ray PF, Dulioust E, Touré A. Cavarocchi E, et al. Among authors: govin j. iScience. 2023 Jul 10;26(8):107354. doi: 10.1016/j.isci.2023.107354. eCollection 2023 Aug 18. iScience. 2023. PMID: 37520705 Free PMC article.
Histone Deacetylases and Their Inhibition in Candida Species.
Garnaud C, Champleboux M, Maubon D, Cornet M, Govin J. Garnaud C, et al. Among authors: govin j. Front Microbiol. 2016 Aug 5;7:1238. doi: 10.3389/fmicb.2016.01238. eCollection 2016. Front Microbiol. 2016. PMID: 27547205 Free PMC article. Review.
Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomaly.
Thomas Q, Motta M, Gautier T, Zaki MS, Ciolfi A, Paccaud J, Girodon F, Boespflug-Tanguy O, Besnard T, Kerkhof J, McConkey H, Masson A, Denommé-Pichon AS, Cogné B, Trochu E, Vignard V, El It F, Rodan LH, Alkhateeb MA, Jamra RA, Duplomb L, Tisserant E, Duffourd Y, Bruel AL, Jackson A, Banka S, McEntagart M, Saggar A, Gleeson JG, Sievert D, Bae H, Lee BH, Kwon K, Seo GH, Lee H, Saeed A, Anjum N, Cheema H, Alawbathani S, Khan I, Pinto-Basto J, Teoh J, Wong J, Sahari UBM, Houlden H, Zhelcheska K, Pannetier M, Awad MA, Lesieur-Sebellin M, Barcia G, Amiel J, Delanne J, Philippe C, Faivre L, Odent S, Bertoli-Avella A, Thauvin C, Sadikovic B, Reversade B, Maroofian R, Govin J, Tartaglia M, Vitobello A. Thomas Q, et al. Among authors: govin j. Am J Hum Genet. 2022 Oct 6;109(10):1909-1922. doi: 10.1016/j.ajhg.2022.08.008. Epub 2022 Aug 30. Am J Hum Genet. 2022. PMID: 36044892 Free PMC article.
Establishment of male-specific epigenetic information.
Rousseaux S, Caron C, Govin J, Lestrat C, Faure AK, Khochbin S. Rousseaux S, et al. Among authors: govin j. Gene. 2005 Jan 31;345(2):139-53. doi: 10.1016/j.gene.2004.12.004. Epub 2005 Jan 25. Gene. 2005. PMID: 15716030 Review.
[Organizing the sperm nucleus].
Rousseaux S, Faure AK, Caron C, Lestrat C, Govin J, Hennebicq S, Sèle B, Khochbin S. Rousseaux S, et al. Among authors: govin j. Gynecol Obstet Fertil. 2004 Sep;32(9):785-91. doi: 10.1016/j.gyobfe.2004.07.003. Gynecol Obstet Fertil. 2004. PMID: 15380763 Review. French.
49 results