Francis P - Search Results

1

Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.

Berry V, Francis P, Kaushal S, Moore A, Bhattacharya S. Berry V, et al. Among authors: francis p. Nat Genet. 2000 May;25(1):15-7. doi: 10.1038/75538. Nat Genet. 2000. PMID: 10802646

2

Molecular genetic basis of inherited cataract and associated phenotypes.

Reddy MA, Francis PJ, Berry V, Bhattacharya SS, Moore AT. Reddy MA, et al. Surv Ophthalmol. 2004 May-Jun;49(3):300-15. doi: 10.1016/j.survophthal.2004.02.013. Surv Ophthalmol. 2004. PMID: 15110667 Review.

3

Clinical and genetic heterogeneity in autosomal dominant cataract.

Ionides A, Francis P, Berry V, Mackay D, Bhattacharya S, Shiels A, Moore A. Ionides A, et al. Among authors: francis p. Br J Ophthalmol. 1999 Jul;83(7):802-8. doi: 10.1136/bjo.83.7.802. Br J Ophthalmol. 1999. PMID: 10381667 Free PMC article.

4

Functional impairment of lens aquaporin in two families with dominantly inherited cataracts.

Francis P, Chung JJ, Yasui M, Berry V, Moore A, Wyatt MK, Wistow G, Bhattacharya SS, Agre P. Francis P, et al. Hum Mol Genet. 2000 Sep 22;9(15):2329-34. doi: 10.1093/oxfordjournals.hmg.a018925. Hum Mol Genet. 2000. PMID: 11001937

5

Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).

Francis P, Berry V, Bhattacharya S, Moore A. Francis P, et al. Br J Ophthalmol. 2000 Dec;84(12):1376-9. doi: 10.1136/bjo.84.12.1376. Br J Ophthalmol. 2000. PMID: 11090476 Free PMC article.

6

Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.

Berry V, Francis P, Reddy MA, Collyer D, Vithana E, MacKay I, Dawson G, Carey AH, Moore A, Bhattacharya SS, Quinlan RA. Berry V, et al. Among authors: francis p. Am J Hum Genet. 2001 Nov;69(5):1141-5. doi: 10.1086/324158. Epub 2001 Sep 27. Am J Hum Genet. 2001. PMID: 11577372 Free PMC article.

7

Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene.

Addison PK, Berry V, Ionides AC, Francis PJ, Bhattacharya SS, Moore AT. Addison PK, et al. Among authors: francis pj. Br J Ophthalmol. 2005 Feb;89(2):138-41. doi: 10.1136/bjo.2004.053413. Br J Ophthalmol. 2005. PMID: 15665340 Free PMC article.

8

Lens biology: development and human cataractogenesis.

Francis PJ, Berry V, Moore AT, Bhattacharya S. Francis PJ, et al. Trends Genet. 1999 May;15(5):191-6. doi: 10.1016/s0168-9525(99)01738-2. Trends Genet. 1999. PMID: 10322486 Review.

9

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.

Berry V, Mackay D, Khaliq S, Francis PJ, Hameed A, Anwar K, Mehdi SQ, Newbold RJ, Ionides A, Shiels A, Moore T, Bhattacharya SS. Berry V, et al. Among authors: francis pj. Hum Genet. 1999 Jul-Aug;105(1-2):168-70. doi: 10.1007/s004399900094. Hum Genet. 1999. PMID: 10480374

10

The genetics of childhood cataract.

Francis PJ, Berry V, Bhattacharya SS, Moore AT. Francis PJ, et al. J Med Genet. 2000 Jul;37(7):481-8. doi: 10.1136/jmg.37.7.481. J Med Genet. 2000. PMID: 10882749 Free PMC article. Review.

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