Kelsell DP - Search Results

1

Cellular biomechanics impairment in keratinocytes is associated with a C-terminal truncated desmoplakin: An atomic force microscopy investigation.

Puzzi L, Borin D, Martinelli V, Mestroni L, Kelsell DP, Sbaizero O. Puzzi L, et al. Among authors: kelsell dp. Micron. 2018 Mar;106:27-33. doi: 10.1016/j.micron.2017.12.005. Epub 2017 Dec 19. Micron. 2018. PMID: 29291530 Free article.

2

The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes.

Cabral RM, Tattersall D, Patel V, McPhail GD, Hatzimasoura E, Abrams DJ, South AP, Kelsell DP. Cabral RM, et al. Among authors: kelsell dp. J Cell Sci. 2012 Jun 15;125(Pt 12):2853-61. doi: 10.1242/jcs.084152. Epub 2012 Mar 27. J Cell Sci. 2012. PMID: 22454510

3

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma.

Norgett EE, Hatsell SJ, Carvajal-Huerta L, Cabezas JC, Common J, Purkis PE, Whittock N, Leigh IM, Stevens HP, Kelsell DP. Norgett EE, et al. Among authors: kelsell dp. Hum Mol Genet. 2000 Nov 1;9(18):2761-6. doi: 10.1093/hmg/9.18.2761. Hum Mol Genet. 2000. PMID: 11063735

4

Whats new in genodermatoses?

Fear MW, Hatsell SJ, Leigh IM, Kelsell DP. Fear MW, et al. Among authors: kelsell dp. Keio J Med. 2001 Mar;50(1):35-8. doi: 10.2302/kjm.50.35. Keio J Med. 2001. PMID: 11296663 Free article.

5

Functional studies of human skin disease- and deafness-associated connexin 30 mutations.

Common JE, Becker D, Di WL, Leigh IM, O'Toole EA, Kelsell DP. Common JE, et al. Among authors: kelsell dp. Biochem Biophys Res Commun. 2002 Nov 15;298(5):651-6. doi: 10.1016/s0006-291x(02)02517-2. Biochem Biophys Res Commun. 2002. PMID: 12419304

6

Cellular mechanisms of mutant connexins in skin disease and hearing loss.

Common JE, Di WL, Davies D, Galvin H, Leigh IM, O'Toole EA, Kelsell DP. Common JE, et al. Among authors: kelsell dp. Cell Commun Adhes. 2003 Jul-Dec;10(4-6):347-51. doi: 10.1080/cac.10.4-6.347.351. Cell Commun Adhes. 2003. PMID: 14681040

7

Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.

Di WL, Gu Y, Common JE, Aasen T, O'Toole EA, Kelsell DP, Zicha D. Di WL, et al. Among authors: kelsell dp. J Cell Sci. 2005 Apr 1;118(Pt 7):1505-14. doi: 10.1242/jcs.01733. Epub 2005 Mar 15. J Cell Sci. 2005. PMID: 15769851 Free article.

8

EKV mutant connexin 31 associated cell death is mediated by ER stress.

Tattersall D, Scott CA, Gray C, Zicha D, Kelsell DP. Tattersall D, et al. Among authors: kelsell dp. Hum Mol Genet. 2009 Dec 15;18(24):4734-45. doi: 10.1093/hmg/ddp436. Epub 2009 Sep 14. Hum Mol Genet. 2009. PMID: 19755382 Free PMC article.

9

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children.

Cabral RM, Liu L, Hogan C, Dopping-Hepenstal PJ, Winik BC, Asial RA, Dobson R, Mein CA, Baselaga PA, Mellerio JE, Nanda A, Boente Mdel C, Kelsell DP, McGrath JA, South AP. Cabral RM, et al. Among authors: kelsell dp. J Invest Dermatol. 2010 Jun;130(6):1543-50. doi: 10.1038/jid.2010.7. Epub 2010 Feb 4. J Invest Dermatol. 2010. PMID: 20130592 Free article.

10

Insights into desmosome biology from inherited human skin disease and cardiocutaneous syndromes.

Nitoiu D, Etheridge SL, Kelsell DP. Nitoiu D, et al. Among authors: kelsell dp. Cell Commun Adhes. 2014 Jun;21(3):129-40. doi: 10.3109/15419061.2014.908854. Epub 2014 Apr 16. Cell Commun Adhes. 2014. PMID: 24738885 Review.

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