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Items: 9


Phenotypic and functional characterization of Bst+/- mouse retina.

Riazifar H, Sun G, Wang X, Rupp A, Vemaraju S, Ross-Cisneros FN, Lang RA, Sadun AA, Hattar S, Guan MX, Huang T.

Dis Model Mech. 2015 Aug 1;8(8):969-76. doi: 10.1242/dmm.018176. Epub 2015 May 8.


Connecting the retina to the brain.

Erskine L, Herrera E.

ASN Neuro. 2014 Dec 12;6(6). pii: 1759091414562107. doi: 10.1177/1759091414562107. Print 2014. Review.


The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival.

Barkić M, Crnomarković S, Grabusić K, Bogetić I, Panić L, Tamarut S, Cokarić M, Jerić I, Vidak S, Volarević S.

Mol Cell Biol. 2009 May;29(10):2489-504. doi: 10.1128/MCB.01588-08. Epub 2009 Mar 9.


Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute.

Oliver ER, Saunders TL, Tarlé SA, Glaser T.

Development. 2004 Aug;131(16):3907-20.


Genetic factors of age-related macular degeneration.

Tuo J, Bojanowski CM, Chan CC.

Prog Retin Eye Res. 2004 Mar;23(2):229-49. Review.


Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus.

Delettre C, Lenaers G, Belenguer P, Hamel CP.

BMC Genet. 2003 May 7;4:8.


Math5 is required for retinal ganglion cell and optic nerve formation.

Brown NL, Patel S, Brzezinski J, Glaser T.

Development. 2001 Jul;128(13):2497-508.


The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization.

Smith RS, John SW, Zabeleta A, Davisson MT, Hawes NL, Chang B.

Proc Natl Acad Sci U S A. 2000 Feb 29;97(5):2191-5.


Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Votruba M, Moore AT, Bhattacharya SS.

J Med Genet. 1998 Oct;35(10):793-800. Review.

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