Similar articles for PMID: 19202056

Year	Number of Results
1973	1
1990	1
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1996	3
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1998	2
1999	4
2000	7
2001	1
2002	4
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2004	3
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2006	3
2008	2
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2012	8
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2014	7
2015	5
2016	4
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2018	3
2019	6
2021	3
2022	2
2023	2
2024	0

1

Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function.

Blasius AL, Brandl K, Crozat K, Xia Y, Khovananth K, Krebs P, Smart NG, Zampolli A, Ruggeri ZM, Beutler BA. Blasius AL, et al. Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2706-11. doi: 10.1073/pnas.0813208106. Epub 2009 Feb 6. Proc Natl Acad Sci U S A. 2009. PMID: 19202056 Free PMC article.

2

The atypical Guanine-nucleotide exchange factor, dock7, negatively regulates schwann cell differentiation and myelination.

Yamauchi J, Miyamoto Y, Hamasaki H, Sanbe A, Kusakawa S, Nakamura A, Tsumura H, Maeda M, Nemoto N, Kawahara K, Torii T, Tanoue A. Yamauchi J, et al. J Neurosci. 2011 Aug 31;31(35):12579-92. doi: 10.1523/JNEUROSCI.2738-11.2011. J Neurosci. 2011. PMID: 21880919 Free PMC article.

3

Spontaneous mutation of Dock7 results in lower trabecular bone mass and impaired periosteal expansion in aged female Misty mice.

Le PT, Bishop KA, Maridas DE, Motyl KJ, Brooks DJ, Nagano K, Baron R, Bouxsein ML, Rosen CJ. Le PT, et al. Bone. 2017 Dec;105:103-114. doi: 10.1016/j.bone.2017.08.006. Epub 2017 Aug 15. Bone. 2017. PMID: 28821457 Free PMC article.

4

The murine misty mutation: phenotypic effects on melanocytes, platelets and brown fat.

Sviderskaya EV, Novak EK, Swank RT, Bennett DC. Sviderskaya EV, et al. Genetics. 1998 Jan;148(1):381-90. doi: 10.1093/genetics/148.1.381. Genetics. 1998. PMID: 9475748 Free PMC article.

5

Altered thermogenesis and impaired bone remodeling in Misty mice.

Motyl KJ, Bishop KA, DeMambro VE, Bornstein SA, Le P, Kawai M, Lotinun S, Horowitz MC, Baron R, Bouxsein ML, Rosen CJ. Motyl KJ, et al. J Bone Miner Res. 2013 Sep;28(9):1885-97. doi: 10.1002/jbmr.1943. J Bone Miner Res. 2013. PMID: 23553822 Free PMC article.

6

Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.

Perrault I, Hamdan FF, Rio M, Capo-Chichi JM, Boddaert N, Décarie JC, Maranda B, Nabbout R, Sylvain M, Lortie A, Roux PP, Rossignol E, Gérard X, Barcia G, Berquin P, Munnich A, Rouleau GA, Kaplan J, Rozet JM, Michaud JL. Perrault I, et al. Am J Hum Genet. 2014 Jun 5;94(6):891-7. doi: 10.1016/j.ajhg.2014.04.012. Epub 2014 May 8. Am J Hum Genet. 2014. PMID: 24814191 Free PMC article.

7

CRISPR/Cas9-Mediated Insertion of loxP Sites in the Mouse Dock7 Gene Provides an Effective Alternative to Use of Targeted Embryonic Stem Cells.

Bishop KA, Harrington A, Kouranova E, Weinstein EJ, Rosen CJ, Cui X, Liaw L. Bishop KA, et al. G3 (Bethesda). 2016 Jul 7;6(7):2051-61. doi: 10.1534/g3.116.030601. G3 (Bethesda). 2016. PMID: 27175020 Free PMC article.

8

The transcription factors Ets1 and Sox10 interact during murine melanocyte development.

Saldana-Caboverde A, Perera EM, Watkins-Chow DE, Hansen NF, Vemulapalli M, Mullikin JC; NISC Comparative Sequencing Program; Pavan WJ, Kos L. Saldana-Caboverde A, et al. Dev Biol. 2015 Nov 15;407(2):300-12. doi: 10.1016/j.ydbio.2015.04.012. Epub 2015 Apr 23. Dev Biol. 2015. PMID: 25912689 Free PMC article.

9

Guanine nucleotide exchange factor Dock7 mediates HGF-induced glioblastoma cell invasion via Rac activation.

Murray DW, Didier S, Chan A, Paulino V, Van Aelst L, Ruggieri R, Tran NL, Byrne AT, Symons M. Murray DW, et al. Br J Cancer. 2014 Mar 4;110(5):1307-15. doi: 10.1038/bjc.2014.39. Epub 2014 Feb 11. Br J Cancer. 2014. PMID: 24518591 Free PMC article.

10

Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment.

Kivrak Pfiffner F, Koller S, Ménétrey A, Graf U, Bähr L, Maspoli A, Hackenberg A, Kottke R, Gerth-Kahlert C, Berger W. Kivrak Pfiffner F, et al. Int J Mol Sci. 2022 Jul 2;23(13):7382. doi: 10.3390/ijms23137382. Int J Mol Sci. 2022. PMID: 35806387 Free PMC article.

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