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16 results
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Immunolocalization of Zic2 expression in the developing mouse forebrain.
Brown LY, Kottmann AH, Brown S. Brown LY, et al. Gene Expr Patterns. 2003 Jun;3(3):361-7. doi: 10.1016/s1567-133x(03)00043-7. Gene Expr Patterns. 2003. PMID: 12799086
Zic2 is expressed in pluripotent cells in the blastocyst and adult brain expression overlaps with makers of neurogenesis.
Brown L, Brown S. Brown L, et al. Gene Expr Patterns. 2009 Jan;9(1):43-9. doi: 10.1016/j.gep.2008.08.002. Epub 2008 Aug 12. Gene Expr Patterns. 2009. PMID: 18755297
Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene.
Brown LY, Hodge SE, Johnson WG, Guy SG, Nye JS, Brown S. Brown LY, et al. Am J Med Genet. 2002 Mar 1;108(2):128-31. doi: 10.1002/ajmg.10221. Am J Med Genet. 2002. PMID: 11857562
Zic2 patterns binocular vision by specifying the uncrossed retinal projection.
Herrera E, Brown L, Aruga J, Rachel RA, Dolen G, Mikoshiba K, Brown S, Mason CA. Herrera E, et al. Cell. 2003 Sep 5;114(5):545-57. doi: 10.1016/s0092-8674(03)00684-6. Cell. 2003. PMID: 13678579
In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation.
Brown L, Paraso M, Arkell R, Brown S. Brown L, et al. Hum Mol Genet. 2005 Feb 1;14(3):411-20. doi: 10.1093/hmg/ddi037. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590697
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
Brown SA, Warburton D, Brown LY, Yu CY, Roeder ER, Stengel-Rutkowski S, Hennekam RC, Muenke M. Brown SA, et al. Among authors: brown ly. Nat Genet. 1998 Oct;20(2):180-3. doi: 10.1038/2484. Nat Genet. 1998. PMID: 9771712
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
Brown LY, Odent S, David V, Blayau M, Dubourg C, Apacik C, Delgado MA, Hall BD, Reynolds JF, Sommer A, Wieczorek D, Brown SA, Muenke M. Brown LY, et al. Hum Mol Genet. 2001 Apr 1;10(8):791-6. doi: 10.1093/hmg/10.8.791. Hum Mol Genet. 2001. PMID: 11285244
Alanine tracts: the expanding story of human illness and trinucleotide repeats.
Brown LY, Brown SA. Brown LY, et al. Trends Genet. 2004 Jan;20(1):51-8. doi: 10.1016/j.tig.2003.11.002. Trends Genet. 2004. PMID: 14698619 Review.
Validation of QF-PCR for prenatal aneuploidy screening in the United States.
Brown L, Abigania M, Warburton D, Brown S. Brown L, et al. Prenat Diagn. 2006 Nov;26(11):1068-74. doi: 10.1002/pd.1558. Prenat Diagn. 2006. PMID: 16952193
Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report.
Brown LY, Alonso ML, Yu J, Warburton D, Brown S. Brown LY, et al. Among authors: brown s. Prenat Diagn. 2001 Jan;21(1):27-30. doi: 10.1002/1097-0223(200101)21:1<27::aid-pd971>;2-r. Prenat Diagn. 2001. PMID: 11180236
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