PubMed ID: 15364238 Author(s): Tamhankar MA, Liu GT, Young TL, Sutton LN, Hurst RW. Acquired, isolated third nerve palsies in infants with cerebrovascular malformations. Am J Ophthalmol. 2004 Sep;138(3):484-6. PMID 15364238 Journal: American Journal Of …
Young Lab
Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia.
PubMed ID: 15223781 Author(s): Scavello GS, Paluru PC, Ganter WR, Young TL. Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia. Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2091-7. PMID …
X-linked high myopia associated with cone dysfunction.
PubMed ID: 15197065 Author(s): Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky …
Microarray analysis of gene expression in human donor sclera.
PubMed ID: 15041956 Author(s): Young TL, Scavello GS, Paluru PC, Choi JD, Rappaport EF, Rada JA. Microarray analysis of gene expression in human donor sclera. Mol Vis. 2004 Mar 22;10:163-76. PMID 15041956 Journal: Molecular Vision, …
Dissecting the genetics of human high myopia: a molecular biologic approach.
PubMed ID: 15747770 Author(s): Young TL. Dissecting the genetics of human high myopia: a molecular biologic approach. Trans Am Ophthalmol Soc. 2004;102:423-45. PMID 15747770 Journal: Transactions Of The American Ophthalmological Society, Volume 102, 2004 PURPOSE …
Identification of genes expressed in a human scleral cDNA library.
PubMed ID: 14551531 Author(s): Young TL, Guo XD, King RA, Johnson JM, Rada JA. Identification of genes expressed in a human scleral cDNA library. Mol Vis. 2003 Oct 7;9:508-14. PMID 14551531 Journal: Molecular Vision, Volume …
Ophthalmic genetics/inherited eye disease.
PubMed ID: 14502058 Author(s): Young TL. Ophthalmic genetics/inherited eye disease. Curr Opin Ophthalmol. 2003 Oct;14(5):296-303. Review. PMID 14502058 Journal: Current Opinion In Ophthalmology, Volume 14, Issue 5, Oct 2003 PURPOSE OF REVIEW Genetic diseases of …
New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.
PubMed ID: 12714612 Author(s): Paluru P, Ronan SM, Heon E, Devoto M, Wildenberg SC, Scavello G, Holleschau A, Mäkitie O, Cole WG, King RA, Young TL. New locus for autosomal dominant high myopia maps to …
Retinal neovascular markers in retinopathy of prematurity: aetiological implications.
PubMed ID: 12598436 Author(s): North PE, Anthony DC, Young TL, Waner M, Brown HH, Brodsky MC. Retinal neovascular markers in retinopathy of prematurity: aetiological implications. Br J Ophthalmol. 2003 Mar;87(3):275-8. PMID 12598436 Journal: The British …