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Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants.
Chapman G, Moreau JLM, I P E, Szot JO, Iyer KR, Shi H, Yam MX, O'Reilly VC, Enriquez A, Greasby JA, Alankarage D, Martin EMMA, Hanna BC, Edwards M, Monger S, Blue GM, Winlaw DS, Ritchie HE, Grieve SM, Giannoulatou E, Sparrow DB, Dunwoodie SL. Chapman G, et al. Among authors: sparrow db. Hum Mol Genet. 2020 Mar 13;29(4):566-579. doi: 10.1093/hmg/ddz270. Hum Mol Genet. 2020. PMID: 31813956 Free PMC article.
Diverse requirements for Notch signalling in mammals.
Sparrow DB, Clements M, Withington SL, Scott AN, Novotny J, Sillence D, Kusumi K, Beddington RS, Dunwoodie SL. Sparrow DB, et al. Int J Dev Biol. 2002;46(4):365-74. Int J Dev Biol. 2002. PMID: 12141422
Kousseff syndrome: a causally heterogeneous disorder.
Maclean K, Field MJ, Colley AS, Mowat DR, Sparrow DB, Dunwoodie SL, Kirk EP. Maclean K, et al. Among authors: sparrow db. Am J Med Genet A. 2004 Jan 30;124A(3):307-12. doi: 10.1002/ajmg.a.20418. Am J Med Genet A. 2004. PMID: 14708106
Mutated MESP2 causes spondylocostal dysostosis in humans.
Whittock NV, Sparrow DB, Wouters MA, Sillence D, Ellard S, Dunwoodie SL, Turnpenny PD. Whittock NV, et al. Among authors: sparrow db. Am J Hum Genet. 2004 Jun;74(6):1249-54. doi: 10.1086/421053. Epub 2004 Apr 30. Am J Hum Genet. 2004. PMID: 15122512 Free PMC article.
Evolution of distinct EGF domains with specific functions.
Wouters MA, Rigoutsos I, Chu CK, Feng LL, Sparrow DB, Dunwoodie SL. Wouters MA, et al. Among authors: sparrow db. Protein Sci. 2005 Apr;14(4):1091-103. doi: 10.1110/ps.041207005. Protein Sci. 2005. PMID: 15772310 Free PMC article.
Generation of conditional Cited2 null alleles.
Preis JI, Wise N, Solloway MJ, Harvey RP, Sparrow DB, Dunwoodie SL. Preis JI, et al. Among authors: sparrow db. Genesis. 2006 Dec;44(12):579-83. doi: 10.1002/dvg.20251. Genesis. 2006. PMID: 17133411
66 results