Proteomic profiling of human intraschisis cavity fluid

The proteome of normal human retrobulbar optic nerve and sclera

(2016) Pingbo Zhang et al.   PROTEOMICS

Defining the proteome of human iris, ciliary body, retinal pigment epithelium, and choroid

(2016) Pingbo Zhang et al.   PROTEOMICS

The proteome of human retina

(2015) Pingbo Zhang et al.   PROTEOMICS

FunRich: An open access standalone functional enrichment and interaction network analysis tool

(2015) Mohashin Pathan et al.   PROTEOMICS

Inhibition of the alternative complement pathway preserves photoreceptors after retinal injury

(2015) J. Harry Sweigard et al.   Science Translational Medicine

Increased expression of ESCO1 is correlated with poor patient survival and its role in human bladder cancer

(2015) Shiying Zhang et al.   TUMOR BIOLOGY

Sequencing of Candidate Chromosome Instability Genes in Endometrial Cancers Reveals Somatic Mutations in ESCO1, CHTF18, and MRE11A

(2014) Jessica C. Price et al.   PLoS One

Enzymology of retinoic acid biosynthesis and degradation

(2013) Natalia Y. Kedishvili   JOURNAL OF LIPID RESEARCH

A search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways

(2013) Mark W. Logue et al.   NEUROBIOLOGY OF AGING

In-depth mass spectrometric mapping of the human vitreous proteome

(2013) Sebastian Aretz et al.   Proteome Science

The Human Eye Proteome Project: Perspectives on an emerging proteome

(2013) Richard D. Semba et al.   PROTEOMICS

Mutant GlialCAM Causes Megalencephalic Leukoencephalopathy with Subcortical Cysts, Benign Familial Macrocephaly, and Macrocephaly with Retardation and Autism

(2011) Tania López-Hernández et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

(2011) Fadi F. Hamdan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Age-related macular degeneration and the complement system

(2011) S. Khandhadia et al.   IMMUNOBIOLOGY

The complement system

(2010) J. Vidya Sarma et al.   CELL AND TISSUE RESEARCH

Molecular Mechanisms Leading to Null-Protein Product from Retinoschisin (RS1) Signal-Sequence Mutants in X-Linked Retinoschisis (XLRS) Disease

(2010) Camasamudram Vijayasarathy et al.   HUMAN MUTATION

A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

(2008) Alexander G. Bassuk et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ISCEV Standard for full-field clinical electroretinography (2008 update)

(2008) M. F. Marmor et al.   DOCUMENTA OPHTHALMOLOGICA