Chapman G - Search Results

1

Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders.

Szot JO, Campagnolo C, Cao Y, Iyer KR, Cuny H, Drysdale T, Flores-Daboub JA, Bi W, Westerfield L, Liu P, Leung TN, Choy KW, Chapman G, Xiao R, Siu VM, Dunwoodie SL. Szot JO, et al. Among authors: chapman g. Am J Hum Genet. 2020 Jan 2;106(1):129-136. doi: 10.1016/j.ajhg.2019.12.006. Epub 2019 Dec 26. Am J Hum Genet. 2020. PMID: 31883644 Free PMC article.

2

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.

Sparrow DB, Chapman G, Wouters MA, Whittock NV, Ellard S, Fatkin D, Turnpenny PD, Kusumi K, Sillence D, Dunwoodie SL. Sparrow DB, et al. Among authors: chapman g. Am J Hum Genet. 2006 Jan;78(1):28-37. doi: 10.1086/498879. Epub 2005 Nov 16. Am J Hum Genet. 2006. PMID: 16385447 Free PMC article.

3

Disruption of the somitic molecular clock causes abnormal vertebral segmentation.

Sparrow DB, Chapman G, Turnpenny PD, Dunwoodie SL. Sparrow DB, et al. Among authors: chapman g. Birth Defects Res C Embryo Today. 2007 Jun;81(2):93-110. doi: 10.1002/bdrc.20093. Birth Defects Res C Embryo Today. 2007. PMID: 17600782 Review.

4

Role of Delta-like-3 in mammalian somitogenesis and vertebral column formation.

Chapman G, Dunwoodie SL. Chapman G, et al. Adv Exp Med Biol. 2008;638:95-112. doi: 10.1007/978-0-387-09606-3_5. Adv Exp Med Biol. 2008. PMID: 21038772 Review.

5

Notch inhibition by the ligand DELTA-LIKE 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis.

Chapman G, Sparrow DB, Kremmer E, Dunwoodie SL. Chapman G, et al. Hum Mol Genet. 2011 Mar 1;20(5):905-16. doi: 10.1093/hmg/ddq529. Epub 2010 Dec 7. Hum Mol Genet. 2011. PMID: 21147753

6

A cell autonomous role for the Notch ligand Delta-like 3 in αβ T-cell development.

Hoyne GF, Chapman G, Sontani Y, Pursglove SE, Dunwoodie SL. Hoyne GF, et al. Among authors: chapman g. Immunol Cell Biol. 2011 Aug;89(6):696-705. doi: 10.1038/icb.2010.154. Epub 2010 Dec 14. Immunol Cell Biol. 2011. PMID: 21151194

7

Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis.

Lopes Floro K, Artap ST, Preis JI, Fatkin D, Chapman G, Furtado MB, Harvey RP, Hamada H, Sparrow DB, Dunwoodie SL. Lopes Floro K, et al. Among authors: chapman g. Hum Mol Genet. 2011 Mar 15;20(6):1097-110. doi: 10.1093/hmg/ddq554. Epub 2010 Dec 28. Hum Mol Genet. 2011. PMID: 21224256

8

The mouse notches up another success: understanding the causes of human vertebral malformation.

Sparrow DB, Chapman G, Dunwoodie SL. Sparrow DB, et al. Among authors: chapman g. Mamm Genome. 2011 Aug;22(7-8):362-76. doi: 10.1007/s00335-011-9335-5. Epub 2011 Jun 11. Mamm Genome. 2011. PMID: 21667129 Review.

9

Cooperation between somatic Ikaros and Notch1 mutations at the inception of T-ALL.

Sontani Y, Chapman G, Papathanasiou P, Dunwoodie S, Goodnow CC, Hoyne GF. Sontani Y, et al. Among authors: chapman g. Leuk Res. 2011 Nov;35(11):1512-9. doi: 10.1016/j.leukres.2011.07.024. Epub 2011 Aug 15. Leuk Res. 2011. PMID: 21840596 Free article.

10

A mechanism for gene-environment interaction in the etiology of congenital scoliosis.

Sparrow DB, Chapman G, Smith AJ, Mattar MZ, Major JA, O'Reilly VC, Saga Y, Zackai EH, Dormans JP, Alman BA, McGregor L, Kageyama R, Kusumi K, Dunwoodie SL. Sparrow DB, et al. Among authors: chapman g. Cell. 2012 Apr 13;149(2):295-306. doi: 10.1016/j.cell.2012.02.054. Epub 2012 Apr 5. Cell. 2012. PMID: 22484060 Free article.

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