Results 131 to 140 of about 8,769 (230)

Identification and functional characterization of a novel CRYBB1 deletion mutation causing autosomal dominant congenital cataract in a Chinese family. [PDF]

BMC Ophthalmol
Li L, Yue J, Song J, Qin M, Zhou S, Liu J, Zheng G.   +6 more
europepmc   +1 more source

Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling [PDF]

, 2011
Robert C Day, Caroline W Beck
core   +1 more source

Identification of Age- and Cataract-Related Changes in High-Density Lens Protein Aggregates. [PDF]

Invest Ophthalmol Vis Sci
Wang Z, Friedrich MG, Truscott RJW, Schey KL.   +3 more
europepmc   +1 more source

A missense mutation in the γD crystallin gene (CRYGD) associated with autosomal dominant coral-like cataract linked to chromosome 2q [PDF]

, 2004
Andley, Usha P, Mackay, Donna S, Shiels, Alan   +2 more
core   +1 more source

Crystalline Insulin [PDF]

Proceedings of the National Academy of Sciences, 1926
openaire   +2 more sources

Mutation screening of γ-crystallin gene in congenital cataract patients from North India. [PDF]

Indian J Ophthalmol
Fatima AE, Kumar R, Afzal M.
europepmc   +1 more source

Protein aggregation in neurodegenerative diseases. [PDF]

Chin Med J (Engl)
Wang J, Dai L, Zhang Z.
europepmc   +1 more source

Investigation of the Effect of C-Terminal Adjacent Phenylalanine Residues on Asparagine Deamidation by Quantum Chemical Calculations. [PDF]

Int J Mol Sci
Kato K, Asai H, Nakayoshi T, Mizuno A, Oda A, Ishikawa Y.   +5 more
europepmc   +1 more source

The Molecular aspects of biological development [PDF]

Deering, R. A., Pennsylvania State University. Biophysics Dept., Trask, Muriel., United States. National Aeronautics and Space Administration.   +3 more
core   +2 more sources

HuD and alpha-crystallin A axis protects neuro-retinal cells in early diabetes. [PDF]

Mol Cell Biochem
Kim C, Oh S, Park YH.
europepmc   +1 more source