Hejtmancik JF - Search Results

1

Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.

Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF. Riazuddin SA, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2264-70. doi: 10.1167/iovs.04-1280. Invest Ophthalmol Vis Sci. 2005. PMID: 15980210

2

Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.

Padma T, Ayyagari R, Murty JS, Basti S, Fletcher T, Rao GN, Kaiser-Kupfer M, Hejtmancik JF. Padma T, et al. Among authors: hejtmancik jf. Am J Hum Genet. 1995 Oct;57(4):840-5. Am J Hum Genet. 1995. PMID: 7573044 Free PMC article.

3

Autosomal dominant congenital cataract. Interocular phenotypic variability.

Scott MH, Hejtmancik JF, Wozencraft LA, Reuter LM, Parks MM, Kaiser-Kupfer MI. Scott MH, et al. Among authors: hejtmancik jf. Ophthalmology. 1994 May;101(5):866-71. doi: 10.1016/s0161-6420(94)31246-2. Ophthalmology. 1994. PMID: 8190472

4

Autosomal dominant zonular cataract with sutural opacities in a four-generation family.

Basti S, Hejtmancik JF, Padma T, Ayyagari R, Kaiser-Kupfer MI, Murty JS, Rao GN. Basti S, et al. Among authors: hejtmancik jf. Am J Ophthalmol. 1996 Feb;121(2):162-8. doi: 10.1016/s0002-9394(14)70580-x. Am J Ophthalmol. 1996. PMID: 8623885

5

Association properties of betaB2- and betaA3-crystallin: ability to form dimers.

Hejtmancik JF, Wingfield PT, Chambers C, Russell P, Chen HC, Sergeev YV, Hope JN. Hejtmancik JF, et al. Protein Eng. 1997 Nov;10(11):1347-52. doi: 10.1093/protein/10.11.1347. Protein Eng. 1997. PMID: 9514125

6

Local microdomain structure in the terminal extensions of betaA3- and betaB2-crystallins.

Sergeev YV, David LL, Chen HC, Hope JN, Hejtmancik JF. Sergeev YV, et al. Among authors: hejtmancik jf. Mol Vis. 1998 Jun 18;4:9. Mol Vis. 1998. PMID: 9636238 Free article.

7

A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract.

Ren Z, Li A, Shastry BS, Padma T, Ayyagari R, Scott MH, Parks MM, Kaiser-Kupfer MI, Hejtmancik JF. Ren Z, et al. Among authors: hejtmancik jf. Hum Genet. 2000 May;106(5):531-7. doi: 10.1007/s004390000289. Hum Genet. 2000. PMID: 10914683 Free article.

8

Monomer-dimer equilibrium of normal and modified beta A3-crystallins: experimental determination and molecular modeling.

Sergeev YV, Wingfield PT, Hejtmancik JF. Sergeev YV, et al. Among authors: hejtmancik jf. Biochemistry. 2000 Dec 26;39(51):15799-806. doi: 10.1021/bi001882h. Biochemistry. 2000. PMID: 11123905

9

The metabolism of fatty acids in human Bietti crystalline dystrophy.

Lee J, Jiao X, Hejtmancik JF, Kaiser-Kupfer M, Gahl WA, Markello TC, Guo J, Chader GJ. Lee J, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2001 Jul;42(8):1707-14. Invest Ophthalmol Vis Sci. 2001. PMID: 11431432

10

Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?

Tsilou ET, Rubin BI, Caruso RC, Reed GF, Pikus A, Hejtmancik JF, Iwata F, Redman JB, Kaiser-Kupfer MI. Tsilou ET, et al. Among authors: hejtmancik jf. Acta Ophthalmol Scand. 2002 Apr;80(2):196-201. doi: 10.1034/j.1600-0420.2002.800215.x. Acta Ophthalmol Scand. 2002. PMID: 11952489 Free article.

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