Fatkin D - Search Results

1

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.

Tarr I, Hesselson S, Iismaa SE, Rath E, Monger S, Troup M, Mishra K, Wong CMY, Hsu PC, Junday K, Humphreys DT, Adlam D, Webb TR, Baranowska-Clarke AA, Hamby SE, Carss KJ, Samani NJ, Bax M, McGrath-Cadell L, Kovacic JC, Dunwoodie SL, Fatkin D, Muller DWM, Graham RM, Giannoulatou E. Tarr I, et al. Among authors: fatkin d. Circ Genom Precis Med. 2022 Aug;15(4):e003527. doi: 10.1161/CIRCGEN.121.003527. Epub 2022 May 18. Circ Genom Precis Med. 2022. PMID: 35583931 Free PMC article.

2

Prognostic value of left ventricular hypertrophy in hypertrophic cardiomyopathy.

Fatkin D, Graham RM. Fatkin D, et al. N Engl J Med. 2001 Jan 4;344(1):63-5. doi: 10.1056/NEJM200101043440115. N Engl J Med. 2001. PMID: 11187116 No abstract available.

3

Molecular mechanisms of inherited cardiomyopathies.

Fatkin D, Graham RM. Fatkin D, et al. Physiol Rev. 2002 Oct;82(4):945-80. doi: 10.1152/physrev.00012.2002. Physiol Rev. 2002. PMID: 12270949 Free article. Review.

4

Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation.

Stennard FA, Costa MW, Lai D, Biben C, Furtado MB, Solloway MJ, McCulley DJ, Leimena C, Preis JI, Dunwoodie SL, Elliott DE, Prall OW, Black BL, Fatkin D, Harvey RP. Stennard FA, et al. Among authors: fatkin d. Development. 2005 May;132(10):2451-62. doi: 10.1242/dev.01799. Epub 2005 Apr 20. Development. 2005. PMID: 15843414

5

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: fatkin d. 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.

6

Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis.

Sparrow DB, Guillén-Navarro E, Fatkin D, Dunwoodie SL. Sparrow DB, et al. Among authors: fatkin d. Hum Mol Genet. 2008 Dec 1;17(23):3761-6. doi: 10.1093/hmg/ddn272. Epub 2008 Sep 5. Hum Mol Genet. 2008. PMID: 18775957

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: fatkin d. 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

Regulation of murine cardiac contractility by activation of α(1A)-adrenergic receptor-operated Ca(2+) entry.

Mohl MC, Iismaa SE, Xiao XH, Friedrich O, Wagner S, Nikolova-Krstevski V, Wu J, Yu ZY, Feneley M, Fatkin D, Allen DG, Graham RM. Mohl MC, et al. Among authors: fatkin d. Cardiovasc Res. 2011 Jul 15;91(2):310-9. doi: 10.1093/cvr/cvr081. Epub 2011 May 5. Cardiovasc Res. 2011. PMID: 21546445

9

Complexity of murine cardiomyocyte miRNA biogenesis, sequence variant expression and function.

Humphreys DT, Hynes CJ, Patel HR, Wei GH, Cannon L, Fatkin D, Suter CM, Clancy JL, Preiss T. Humphreys DT, et al. Among authors: fatkin d. PLoS One. 2012;7(2):e30933. doi: 10.1371/journal.pone.0030933. Epub 2012 Feb 3. PLoS One. 2012. PMID: 22319597 Free PMC article.

10

A heterozygous variant in the human cardiac miR-133 gene, MIR133A2, alters miRNA duplex processing and strand abundance.

Ohanian M, Humphreys DT, Anderson E, Preiss T, Fatkin D. Ohanian M, et al. Among authors: fatkin d. BMC Genet. 2013 Mar 6;14:18. doi: 10.1186/1471-2156-14-18. BMC Genet. 2013. PMID: 23497314 Free PMC article.

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