Whittock NV[Author] - Search Results

Year	Number of Results
1997	1
1999	2
2000	7
2001	4
2002	6
2003	8
2004	3
2005	1
2006	2
2008	1
2024	0

1

Maroto M, Whittock NV. Maroto M, et al. Among authors: whittock nv. Adv Exp Med Biol. 2008;638:v-vi. Adv Exp Med Biol. 2008. PMID: 21038767 No abstract available.

2

Targetting of desmoglein 1 in inherited and acquired skin diseases.

Whittock NV, Bower C. Whittock NV, et al. Clin Exp Dermatol. 2003 Jul;28(4):410-5. doi: 10.1046/j.1365-2230.2003.01311.x. Clin Exp Dermatol. 2003. PMID: 12823304 Review.

3

New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.

Whittock NV, Ashton GH, Griffiths WA, Eady RA, McGrath JA. Whittock NV, et al. Br J Dermatol. 2001 Aug;145(2):330-5. doi: 10.1046/j.1365-2133.2001.04327.x. Br J Dermatol. 2001. PMID: 11531804 Review.

4

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. 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.

5

The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.

Whittock NV, Coleman CM, McLean WH, Ashton GH, Acland KM, Eady RA, McGrath JA. Whittock NV, et al. J Invest Dermatol. 2000 Oct;115(4):694-8. doi: 10.1046/j.1523-1747.2000.00097.x. J Invest Dermatol. 2000. PMID: 10998145 Free article.

6

Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndrome.

Fassihi H, Grace J, Lashwood A, Whittock NV, Braude PR, Pickering SJ, McGrath JA. Fassihi H, et al. Among authors: whittock nv. Br J Dermatol. 2006 Mar;154(3):546-50. doi: 10.1111/j.1365-2133.2005.07102.x. Br J Dermatol. 2006. PMID: 16445790

7

Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency.

Whittock NV, Ashton GH, Dopping-Hepenstal PJ, Gratian MJ, Keane FM, Eady RA, McGrath JA. Whittock NV, et al. J Invest Dermatol. 1999 Dec;113(6):940-6. doi: 10.1046/j.1523-1747.1999.00783.x. J Invest Dermatol. 1999. PMID: 10594734 Free article.

8

Genomic organization and amplification of the human plakoglobin gene (JUP).

Whittock NV, Eady RA, McGrath JA. Whittock NV, et al. Exp Dermatol. 2000 Oct;9(5):323-6. doi: 10.1034/j.1600-0625.2000.009005323.x. Exp Dermatol. 2000. PMID: 11016852

9

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: whittock nv. 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.

10

Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndrome.

Nagasaka T, Nishifuji K, Ota T, Whittock NV, Amagai M. Nagasaka T, et al. Among authors: whittock nv. J Clin Invest. 2004 Nov;114(10):1484-92. doi: 10.1172/JCI20480. J Clin Invest. 2004. PMID: 15545999 Free PMC article.

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