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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2004 | 2 |
2008 | 1 |
2009 | 1 |
2010 | 1 |
2016 | 2 |
2017 | 1 |
2024 | 0 |
PubMed (cited) for id: 614567
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Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T).
Acta Otorrinolaringol Esp (Engl Ed). 2017 May-Jun;68(3):183-185. doi: 10.1016/j.otorri.2016.06.004. Epub 2016 Sep 19.
Acta Otorrinolaringol Esp (Engl Ed). 2017.
PMID: 27658576
English, Spanish.
No abstract available.
High-throughput discovery of novel developmental phenotypes.
Dickinson ME, Flenniken AM, Ji X, Teboul L, Wong MD, White JK, Meehan TF, Weninger WJ, Westerberg H, Adissu H, Baker CN, Bower L, Brown JM, Caddle LB, Chiani F, Clary D, Cleak J, Daly MJ, Denegre JM, Doe B, Dolan ME, Edie SM, Fuchs H, Gailus-Durner V, Galli A, Gambadoro A, Gallegos J, Guo S, Horner NR, Hsu CW, Johnson SJ, Kalaga S, Keith LC, Lanoue L, Lawson TN, Lek M, Mark M, Marschall S, Mason J, McElwee ML, Newbigging S, Nutter LM, Peterson KA, Ramirez-Solis R, Rowland DJ, Ryder E, Samocha KE, Seavitt JR, Selloum M, Szoke-Kovacs Z, Tamura M, Trainor AG, Tudose I, Wakana S, Warren J, Wendling O, West DB, Wong L, Yoshiki A; International Mouse Phenotyping Consortium; Jackson Laboratory; Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS); Charles River Laboratories; MRC Harwell; Toronto Centre for Phenogenomics; Wellcome Trust Sanger Institute; RIKEN BioResource Center; MacArthur DG, Tocchini-Valentini GP, Gao X, Flicek P, Bradley A, Skarnes WC, Justice MJ, Parkinson HE, Moore M, Wells S, Braun RE, Svenson KL, de Angelis MH, Herault Y, Mohun T, Mallon AM, Henkelman RM, Brown SD, Adams DJ, Lloyd KC, McKerlie C, Beaudet AL, Bućan M, Murray SA.
Dickinson ME, et al.
Nature. 2016 Sep 22;537(7621):508-514. doi: 10.1038/nature19356. Epub 2016 Sep 14.
Nature. 2016.
PMID: 27626380
Free PMC article.
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Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.
Schoen CJ, Emery SB, Thorne MC, Ammana HR, Sliwerska E, Arnett J, Hortsch M, Hannan F, Burmeister M, Lesperance MM.
Schoen CJ, et al.
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13396-401. doi: 10.1073/pnas.1003027107. Epub 2010 Jul 12.
Proc Natl Acad Sci U S A. 2010.
PMID: 20624953
Free PMC article.
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Ubiquitin-mediated degradation of the formin mDia2 upon completion of cell division.
DeWard AD, Alberts AS.
DeWard AD, et al.
J Biol Chem. 2009 Jul 24;284(30):20061-9. doi: 10.1074/jbc.M109.000885. Epub 2009 May 19.
J Biol Chem. 2009.
PMID: 19457867
Free PMC article.
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Filopodia formation induced by active mDia2/Drf3.
Block J, Stradal TE, Hänisch J, Geffers R, Köstler SA, Urban E, Small JV, Rottner K, Faix J.
Block J, et al.
J Microsc. 2008 Sep;231(3):506-17. doi: 10.1111/j.1365-2818.2008.02063.x.
J Microsc. 2008.
PMID: 18755006
Free article.
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A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21.
Kim TB, Isaacson B, Sivakumaran TA, Starr A, Keats BJ, Lesperance MM.
Kim TB, et al.
J Med Genet. 2004 Nov;41(11):872-6. doi: 10.1136/jmg.2004.020628.
J Med Genet. 2004.
PMID: 15520414
Free PMC article.
No abstract available.
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Identification and characterization of human DIAPH3 gene in silico.
Katoh M, Katoh M.
Katoh M, et al.
Int J Mol Med. 2004 Mar;13(3):473-8.
Int J Mol Med. 2004.
PMID: 14767582
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