Hejtmancik JF - Search Results

1

Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts.

Rowan S, Jiang S, Francisco SG, Pomatto LCD, Ma Z, Jiao X, Campos MM, Aryal S, Patel SD, Mahaling B, Riazuddin SA, Duh EJ, Lachke SA, Hejtmancik JF, de Cabo R, FitzGerald PG, Taylor A. Rowan S, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2021 Dec 1;62(15):10. doi: 10.1167/iovs.62.15.10. Invest Ophthalmol Vis Sci. 2021. PMID: 34882206 Free PMC article.

2

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

3

Glutathione S-transferase M1 genotype and age-related cataracts. Lack of association in an Italian population.

Alberti G, Oguni M, Podgor M, Sperduto RD, Tomarev S, Grassi C, Williams S, Kaiser-Kupfer M, Maraini G, Hejtmancik JF. Alberti G, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 1996 May;37(6):1167-73. Invest Ophthalmol Vis Sci. 1996. PMID: 8631631

4

Identification, isolation, and characterization of a 32-kDa fatty acid-binding protein missing from lymphocytes in humans with Bietti crystalline dystrophy (BCD).

Lee J, Jiao X, Hejtmancik JF, Kaiser-Kupfer M, Chader GJ. Lee J, et al. Among authors: hejtmancik jf. Mol Genet Metab. 1998 Oct;65(2):143-54. doi: 10.1006/mgme.1998.2723. Mol Genet Metab. 1998. PMID: 9787106

5

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

6

Cataract- and lens-specific upregulation of ARK receptor tyrosine kinase in Emory mouse cataract.

Sheets NL, Chauhan BK, Wawrousek E, Hejtmancik JF, Cvekl A, Kantorow M. Sheets NL, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1870-5. Invest Ophthalmol Vis Sci. 2002. PMID: 12036992 Free PMC article.

7

Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.

Jiao X, Munier FL, Schorderet DF, Zografos L, Smith J, Rubin B, Hejtmancik JF. Jiao X, et al. Among authors: hejtmancik jf. Hum Genet. 2003 May;112(5-6):593-9. doi: 10.1007/s00439-002-0905-1. Epub 2003 Feb 27. Hum Genet. 2003. PMID: 12607114

8

A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts.

Pras E, Raz J, Yahalom V, Frydman M, Garzozi HJ, Pras E, Hejtmancik JF. Pras E, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1940-5. doi: 10.1167/iovs.03-1117. Invest Ophthalmol Vis Sci. 2004. PMID: 15161861

9

Molecular genetics of age-related cataract.

Hejtmancik JF, Kantorow M. Hejtmancik JF, et al. Exp Eye Res. 2004 Jul;79(1):3-9. doi: 10.1016/j.exer.2004.03.014. Exp Eye Res. 2004. PMID: 15183095 Free PMC article. Review.

10

A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.

Smaoui N, Beltaief O, BenHamed S, M'Rad R, Maazoul F, Ouertani A, Chaabouni H, Hejtmancik JF. Smaoui N, et al. Among authors: hejtmancik jf. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2716-21. doi: 10.1167/iovs.03-1370. Invest Ophthalmol Vis Sci. 2004. PMID: 15277496

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

266 results

Search Page