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Lihua Y Marmorstein

Showing results (1-10 of 37) with videos related to

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Experimental Eye Research|October 6, 2009
Focus on molecules: fibulin-3 (EFEMP1)Youwen Zhang, Lihua Y Marmorstein
Trends in Genetics : TIG|March 21, 2007
The challenge of modeling macular degeneration in miceAlan D Marmorstein, Lihua Y Marmorstein
Biochimica Et Biophysica Acta|August 10, 2014
Soluble adenylyl cyclase in the eyeYong S Lee, Lihua Y Marmorstein, Alan D Marmorstein
Investigative Ophthalmology & Visual Science|June 7, 2011
Relationship of stokes radius to the rate of diffusion across Bruch's membraneAstrid Zayas-Santiago, Alan D Marmorstein, Lihua Y Marmorstein
Investigative Ophthalmology & Visual Science|July 2, 2002
Spectral profiling of autofluorescence associated with lipofuscin, Bruch's Membrane, and sub-RPE deposits in normal and AMD eyesAlan D Marmorstein, Lihua Y Marmorstein, Hirokazu Sakaguchi, et al.
Investigative Ophthalmology & Visual Science|March 7, 2017
Deletion of Efemp1 Is Protective Against the Development of Sub-RPE Deposits in Mouse EyesJames B Stanton, Alan D Marmorstein, Youwen Zhang, et al.
The Journal of Biological Chemistry|May 5, 2004
Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerationsPhilip A Klenotic, Francis L Munier, Lihua Y Marmorstein, et al.
Investigative Ophthalmology & Visual Science|October 27, 2005
Aberrant accumulation of fibulin-3 in the endoplasmic reticulum leads to activation of the unfolded protein response and VEGF expressionC Nathaniel Roybal, Lihua Y Marmorstein, David L Vander Jagt, et al.
Human Molecular Genetics|August 1, 2007
Formation and progression of sub-retinal pigment epithelium deposits in Efemp1 mutation knock-in mice: a model for the early pathogenic course of macular degenerationLihua Y Marmorstein, Precious J McLaughlin, Neal S Peachey, et al.
American Journal of Human Genetics|May 11, 2006
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndromeVishwanathan Hucthagowder, Nina Sausgruber, Katherine H Kim, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Experimental Eye Research|October 6, 2009
Focus on molecules: fibulin-3 (EFEMP1)Youwen Zhang, Lihua Y Marmorstein
Trends in Genetics : TIG|March 21, 2007
The challenge of modeling macular degeneration in miceAlan D Marmorstein, Lihua Y Marmorstein
Biochimica Et Biophysica Acta|August 10, 2014
Soluble adenylyl cyclase in the eyeYong S Lee, Lihua Y Marmorstein, Alan D Marmorstein
Investigative Ophthalmology & Visual Science|June 7, 2011
Relationship of stokes radius to the rate of diffusion across Bruch's membraneAstrid Zayas-Santiago, Alan D Marmorstein, Lihua Y Marmorstein
Investigative Ophthalmology & Visual Science|July 2, 2002
Spectral profiling of autofluorescence associated with lipofuscin, Bruch's Membrane, and sub-RPE deposits in normal and AMD eyesAlan D Marmorstein, Lihua Y Marmorstein, Hirokazu Sakaguchi, et al.
Investigative Ophthalmology & Visual Science|March 7, 2017
Deletion of Efemp1 Is Protective Against the Development of Sub-RPE Deposits in Mouse EyesJames B Stanton, Alan D Marmorstein, Youwen Zhang, et al.
The Journal of Biological Chemistry|May 5, 2004
Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerationsPhilip A Klenotic, Francis L Munier, Lihua Y Marmorstein, et al.
Investigative Ophthalmology & Visual Science|October 27, 2005
Aberrant accumulation of fibulin-3 in the endoplasmic reticulum leads to activation of the unfolded protein response and VEGF expressionC Nathaniel Roybal, Lihua Y Marmorstein, David L Vander Jagt, et al.
Human Molecular Genetics|August 1, 2007
Formation and progression of sub-retinal pigment epithelium deposits in Efemp1 mutation knock-in mice: a model for the early pathogenic course of macular degenerationLihua Y Marmorstein, Precious J McLaughlin, Neal S Peachey, et al.
American Journal of Human Genetics|May 11, 2006
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndromeVishwanathan Hucthagowder, Nina Sausgruber, Katherine H Kim, et al.
Pageof 4