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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1955 2
1964 7
1965 10
1966 4
1967 7
1968 6
1969 3
1970 3
1972 1
1973 1
1975 1
1976 1
1977 3
1978 6
1979 10
1980 2
1981 1
1982 4
1983 2
1984 5
1985 1
1986 3
1987 5
1988 2
1989 2
1990 2
1991 5
1992 4
1993 8
1994 12
1995 5
1996 1
1997 7
1998 5
1999 6
2000 4
2001 7
2002 6
2003 5
2004 9
2005 3
2006 4
2007 9
2008 12
2009 13
2010 12
2011 18
2012 18
2013 18
2014 24
2015 16
2016 22
2017 12
2018 11
2019 13
2020 23
2021 9
2022 33
2023 17
2024 4

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Article type

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Search Results

431 results

Results by year

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Page 1
[Transcriptional control of ciliary genes].
Vieillard J, Jerber J, Durand B. Vieillard J, et al. Among authors: durand b. Med Sci (Paris). 2014 Nov;30(11):968-75. doi: 10.1051/medsci/20143011010. Epub 2014 Nov 10. Med Sci (Paris). 2014. PMID: 25388578 Free article. Review. French.
Predicting veal-calf trading events in France.
Marsot M, Canini L, Janicot S, Lambert J, Vergu E, Durand B. Marsot M, et al. Among authors: durand b. Prev Vet Med. 2022 Dec;209:105782. doi: 10.1016/j.prevetmed.2022.105782. Epub 2022 Oct 19. Prev Vet Med. 2022. PMID: 36306640
Stent evolution for peripheral arterial disease.
Lejay A, Thaveau F, Girsowicz E, Georg Y, Heim F, Durand B, Chakfé N. Lejay A, et al. Among authors: durand b. J Cardiovasc Surg (Torino). 2012 Feb;53(1 Suppl 1):171-9. J Cardiovasc Surg (Torino). 2012. PMID: 22433736 Review.
Growth charts in DYRK1A syndrome.
Lanvin PL, Goronflot T, Isidor B, Nizon M, Durand B, El Chehadeh S, Geneviève D, Ruault V, Fradin M, Pasquier L, Thévenon J, Delobel B, Burglen L, Afenjar A, Faivre L, Francannet C, Guerrot AM, Goldenberg A, Mercier S, Héron D, Lehalle D, Mignot C, Marey I, Charles P, Moutton S, Bézieau S, Bayat A, Piton A, Willems M, Vincent M. Lanvin PL, et al. Among authors: durand b. Am J Med Genet A. 2024 Jan;194(1):9-16. doi: 10.1002/ajmg.a.63412. Epub 2023 Sep 22. Am J Med Genet A. 2024. PMID: 37740550
De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability.
Schalk A, Cousin MA, Dsouza NR, Challman TD, Wain KE, Powis Z, Minks K, Trimouille A, Lasseaux E, Lacombe D, Angelini C, Michaud V, Van-Gils J, Spataro N, Ruiz A, Gabau E, Stolerman E, Washington C, Louie R, Lanpher BC, Kemppainen JL, Innes M, Kooy F, Meuwissen M, Goldenberg A, Lecoquierre F, Vera G, Diderich KEM, Sheidley B, El Achkar CM, Park M, Hamdan FF, Michaud JL, Lewis AJ, Zweier C, Reis A, Wagner M, Weigand H, Journel H, Keren B, Passemard S, Mignot C, van Gassen K, Brilstra EH, Itzikowitz G, O'Heir E, Allen J, Donald KA, Korf BR, Skelton T, Thompson M, Robin NH, Rudy NL, Dobyns WB, Foss K, Zarate YA, Bosanko KA, Alembik Y, Durand B, Tran Mau-Them F, Ranza E, Blanc X, Antonarakis SE, McWalter K, Torti E, Millan F, Dameron A, Tokita M, Zimmermann MT, Klee EW, Piton A, Gerard B. Schalk A, et al. Among authors: durand b. J Med Genet. 2022 Oct;59(10):965-975. doi: 10.1136/jmedgenet-2021-107751. Epub 2021 Dec 15. J Med Genet. 2022. PMID: 34930816 Free PMC article.
431 results