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

Year Number of Results
2005 4
2006 3
2007 2
2008 1
2009 1
2011 2
2012 2
2013 2
2014 1
2016 2
2017 1
2020 1
2021 1
2022 1
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24 results
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Page 1
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: dameron a. J Med Genet. 2021 Dec 15:jmedgenet-2021-107751. doi: 10.1136/jmedgenet-2021-107751. Online ahead of print. J Med Genet. 2021. PMID: 34930816
Microdisplacement printing.
Dameron AA, Hampton JR, Smith RK, Mullen TJ, Gillmor SD, Weiss PS. Dameron AA, et al. Nano Lett. 2005 Sep;5(9):1834-7. doi: 10.1021/nl050981j. Nano Lett. 2005. PMID: 16159233
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity.
Asselin L, Rivera Alvarez J, Heide S, Bonnet CS, Tilly P, Vitet H, Weber C, Bacino CA, Baranaño K, Chassevent A, Dameron A, Faivre L, Hanchard NA, Mahida S, McWalter K, Mignot C, Nava C, Rastetter A, Streff H, Thauvin-Robinet C, Weiss MM, Zapata G, Zwijnenburg PJG, Saudou F, Depienne C, Golzio C, Héron D, Godin JD. Asselin L, et al. Among authors: dameron a. Nat Commun. 2020 May 15;11(1):2441. doi: 10.1038/s41467-020-16294-6. Nat Commun. 2020. PMID: 32415109 Free PMC article.
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
Okur V, Cho MT, Henderson L, Retterer K, Schneider M, Sattler S, Niyazov D, Azage M, Smith S, Picker J, Lincoln S, Tarnopolsky M, Brady L, Bjornsson HT, Applegate C, Dameron A, Willaert R, Baskin B, Juusola J, Chung WK. Okur V, et al. Among authors: dameron a. Hum Genet. 2016 Jul;135(7):699-705. doi: 10.1007/s00439-016-1661-y. Epub 2016 Apr 5. Hum Genet. 2016. PMID: 27048600
Scanning electron microscopy of nanoscale chemical patterns.
Srinivasan C, Mullen TJ, Hohman JN, Anderson ME, Dameron AA, Andrews AM, Dickey EC, Horn MW, Weiss PS. Srinivasan C, et al. Among authors: dameron aa. ACS Nano. 2007 Oct;1(3):191-201. doi: 10.1021/nn7000799. ACS Nano. 2007. PMID: 19206649
Clonally related methicillin-resistant Staphylococcus aureus isolated from short-finned pilot whales (Globicephala macrorhynchus), human volunteers, and a bayfront cetacean rehabilitation facility.
Hower S, Phillips MC, Brodsky M, Dameron A, Tamargo MA, Salazar NC, Jackson CR, Barrett JB, Davidson M, Davis J, Mukherjee S, Ewing RY, Gidley ML, Sinigalliano CD, Johns L, Johnson FE 3rd, Adebanjo O, Plano LR. Hower S, et al. Among authors: dameron a. Microb Ecol. 2013 May;65(4):1024-38. doi: 10.1007/s00248-013-0178-3. Epub 2013 Mar 19. Microb Ecol. 2013. PMID: 23508733
24 results