Doudney K - Search Results

1

Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients.

Doudney K, Ybot-Gonzalez P, Paternotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P. Doudney K, et al. Am J Med Genet A. 2005 Jul 1;136(1):90-2. doi: 10.1002/ajmg.a.30766. Am J Med Genet A. 2005. PMID: 15952208 No abstract available.

2

Epithelial cell polarity genes are required for neural tube closure.

Doudney K, Stanier P. Doudney K, et al. Am J Med Genet C Semin Med Genet. 2005 May 15;135C(1):42-7. doi: 10.1002/ajmg.c.30052. Am J Med Genet C Semin Med Genet. 2005. PMID: 15800847 Review.

3

Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification.

Murdoch JN, Doudney K, Paternotte C, Copp AJ, Stanier P. Murdoch JN, et al. Among authors: doudney k. Hum Mol Genet. 2001 Oct 15;10(22):2593-601. doi: 10.1093/hmg/10.22.2593. Hum Mol Genet. 2001. PMID: 11709546

4

Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects.

Doudney K, Grinham J, Whittaker J, Lynch SA, Thompson D, Moore GE, Copp AJ, Greene ND, Stanier P. Doudney K, et al. Am J Med Genet A. 2009 Jul;149A(7):1585-9. doi: 10.1002/ajmg.a.32937. Am J Med Genet A. 2009. PMID: 19533788 No abstract available.

5

Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.

Robinson A, Escuin S, Doudney K, Vekemans M, Stevenson RE, Greene ND, Copp AJ, Stanier P. Robinson A, et al. Among authors: doudney k. Hum Mutat. 2012 Feb;33(2):440-7. doi: 10.1002/humu.21662. Epub 2011 Dec 20. Hum Mutat. 2012. PMID: 22095531 Free PMC article.

6

Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.

Murdoch JN, Henderson DJ, Doudney K, Gaston-Massuet C, Phillips HM, Paternotte C, Arkell R, Stanier P, Copp AJ. Murdoch JN, et al. Among authors: doudney k. Hum Mol Genet. 2003 Jan 15;12(2):87-98. doi: 10.1093/hmg/ddg014. Hum Mol Genet. 2003. PMID: 12499390

7

Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23.

Doudney K, Murdoch JN, Paternotte C, Bentley L, Gregory S, Copp AJ, Stanier P. Doudney K, et al. Genomics. 2001 Mar 1;72(2):180-92. doi: 10.1006/geno.2000.6463. Genomics. 2001. PMID: 11401431

8

Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.

Doudney K, Murdoch JN, Braybrook C, Paternotte C, Bentley L, Copp AJ, Stanier P. Doudney K, et al. Genomics. 2002 May;79(5):663-70. doi: 10.1006/geno.2002.6757. Genomics. 2002. PMID: 11991715

9

Abnormal folate metabolism in foetuses affected by neural tube defects.

Dunlevy LP, Chitty LS, Burren KA, Doudney K, Stojilkovic-Mikic T, Stanier P, Scott R, Copp AJ, Greene ND. Dunlevy LP, et al. Among authors: doudney k. Brain. 2007 Apr;130(Pt 4):1043-9. doi: 10.1093/brain/awm028. Brain. 2007. PMID: 17438019 Free PMC article.

10

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P. Braybrook C, et al. Among authors: doudney k. Nat Genet. 2001 Oct;29(2):179-83. doi: 10.1038/ng730. Nat Genet. 2001. PMID: 11559848

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