911 related articles for article (PubMed ID: 11586359)
21. Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.
Fujita E; Tanabe Y; Momoi MY; Momoi T
Neurosci Lett; 2012 Jan; 506(2):277-80. PubMed ID: 22133810
[TBL] [Abstract][Full Text] [Related]
22. FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it.
Tanabe Y; Fujita E; Momoi T
Biochem Biophys Res Commun; 2011 Jul; 410(3):593-6. PubMed ID: 21684252
[TBL] [Abstract][Full Text] [Related]
23. [FOXP2: from the specific disorder to the molecular biology of language. I. Aetiological, neuroanatomical, neurophysiological and molecular aspects].
Benítez-Burraco A
Rev Neurol; 2005 Jun 1-15; 40(11):671-82. PubMed ID: 15948071
[TBL] [Abstract][Full Text] [Related]
24. Evaluation of FOXP2 as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
Am J Med Genet; 2002 Jul; 114(5):566-9. PubMed ID: 12116195
[TBL] [Abstract][Full Text] [Related]
25. Modified sound-evoked brainstem potentials in Foxp2 mutant mice.
Kurt S; Groszer M; Fisher SE; Ehret G
Brain Res; 2009 Sep; 1289():30-6. PubMed ID: 19596273
[TBL] [Abstract][Full Text] [Related]
26. 7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder.
Rieger M; Krumbiegel M; Reuter MS; Schützenberger A; Reis A; Zweier C
Am J Med Genet A; 2020 Nov; 182(11):2737-2741. PubMed ID: 32885567
[TBL] [Abstract][Full Text] [Related]
27. Talk of genetics and vice versa.
Pinker S
Nature; 2001 Oct; 413(6855):465-6. PubMed ID: 11586336
[No Abstract] [Full Text] [Related]
28. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25.
Nishimura DY; Swiderski RE; Alward WL; Searby CC; Patil SR; Bennet SR; Kanis AB; Gastier JM; Stone EM; Sheffield VC
Nat Genet; 1998 Jun; 19(2):140-7. PubMed ID: 9620769
[TBL] [Abstract][Full Text] [Related]
29. Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.
Palka C; Alfonsi M; Mohn A; Cerbo R; Guanciali Franchi P; Fantasia D; Morizio E; Stuppia L; Calabrese G; Zori R; Chiarelli F; Palka G
Pediatrics; 2012 Jan; 129(1):e183-8. PubMed ID: 22144704
[TBL] [Abstract][Full Text] [Related]
30. Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.
Takahashi K; Liu FC; Hirokawa K; Takahashi H
J Neurosci Res; 2003 Jul; 73(1):61-72. PubMed ID: 12815709
[TBL] [Abstract][Full Text] [Related]
31. [Genetic factors in the development of language].
Sanjuán J; Tolosa A; Colomer-Revuelta J; Ivorra-Martínez J; Llacer B; Jover M
Rev Neurol; 2010 Mar; 50 Suppl 3():S101-6. PubMed ID: 20200835
[TBL] [Abstract][Full Text] [Related]
32. FoxP2 in song-learning birds and vocal-learning mammals.
Webb DM; Zhang J
J Hered; 2005; 96(3):212-6. PubMed ID: 15618302
[TBL] [Abstract][Full Text] [Related]
33. [Language gene].
Takahashi H
Rinsho Shinkeigaku; 2006 Nov; 46(11):848-50. PubMed ID: 17432197
[TBL] [Abstract][Full Text] [Related]
34. Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.
Saleem RA; Banerjee-Basu S; Berry FB; Baxevanis AD; Walter MA
Hum Mol Genet; 2003 Nov; 12(22):2993-3005. PubMed ID: 14506133
[TBL] [Abstract][Full Text] [Related]
35. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene.
Shu W; Cho JY; Jiang Y; Zhang M; Weisz D; Elder GA; Schmeidler J; De Gasperi R; Sosa MA; Rabidou D; Santucci AC; Perl D; Morrisey E; Buxbaum JD
Proc Natl Acad Sci U S A; 2005 Jul; 102(27):9643-8. PubMed ID: 15983371
[TBL] [Abstract][Full Text] [Related]
36. Speech sound disorder influenced by a locus in 15q14 region.
Stein CM; Millard C; Kluge A; Miscimarra LE; Cartier KC; Freebairn LA; Hansen AJ; Shriberg LD; Taylor HG; Lewis BA; Iyengar SK
Behav Genet; 2006 Nov; 36(6):858-68. PubMed ID: 16786424
[TBL] [Abstract][Full Text] [Related]
37. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
Jamieson RV; Farrar N; Stewart K; Perveen R; Mihelec M; Carette M; Grigg JR; McAvoy JW; Lovicu FJ; Tam PP; Scambler P; Lloyd IC; Donnai D; Black GC
Hum Mutat; 2007 Oct; 28(10):968-77. PubMed ID: 17492639
[TBL] [Abstract][Full Text] [Related]
38. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.
Warburton P; Baird G; Chen W; Morris K; Jacobs BW; Hodgson S; Docherty Z
Am J Med Genet; 2000 Apr; 96(2):228-34. PubMed ID: 10893502
[TBL] [Abstract][Full Text] [Related]
39. The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin.
Mollet G; Salomon R; Gribouval O; Silbermann F; Bacq D; Landthaler G; Milford D; Nayir A; Rizzoni G; Antignac C; Saunier S
Nat Genet; 2002 Oct; 32(2):300-5. PubMed ID: 12244321
[TBL] [Abstract][Full Text] [Related]
40. Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2.
Tomblin JB; O'Brien M; Shriberg LD; Williams C; Murray J; Patil S; Bjork J; Anderson S; Ballard K
J Speech Lang Hear Res; 2009 Oct; 52(5):1157-74. PubMed ID: 19797137
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]