Compounds > cysteine

cysteine and Eye Abnormalities

cysteine has been researched along with Eye Abnormalities in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	2 (28.57)	18.2507
2000's	2 (28.57)	29.6817
2010's	1 (14.29)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Andley, UP; Reilly, MA	1
Eccles, MR; Walker, RJ; Wilson, JC; Yoon, HS	1
Liu, J; Wang, J; Zhang, Q	1
MacDonald, A; Niemann, WH; Sturman, JA; Wen, GY; Wisniewski, HM	1
Bartlett, SP; Gripp, KW; Katowitz, JA; Markowitz, RI; McDonald-McGinn, DM; Muenke, M; Stolle, CA; Zackai, EH	1
Casci, T; Freeman, M; Vinós, J	1
Ampola, MG; Bixby, EM; Efron, ML; Meshorer, E	1

Other Studies

7 other study(ies) available for cysteine and Eye Abnormalities

Article	Year
Quantitative biometric phenotype analysis in mouse lenses. Molecular vision, 2010, Jun-08, Volume: 16 Topics: Aging; alpha-Crystallin A Chain; Animals; Arginine; Biometry; Cataract; Cysteine; Eye Abnormalities; Genotype; Heterozygote; Homozygote; Image Processing, Computer-Assisted; Lens, Crystalline; Mice; Mice, Knockout; Mice, Transgenic; Mutation; Organ Size; Phenotype; Solubility	2010
A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2007, Volume: 22, Issue:5 Topics: Adult; Aged; Biopsy; Collagen Type IV; Cysteine; Eye Abnormalities; Female; Genetic Linkage; Glomerular Basement Membrane; Hearing Loss; Humans; Kidney; Male; Middle Aged; Mutation; Nephritis, Hereditary; New Zealand; Pedigree; Renal Insufficiency; Tyrosine	2007
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome. Molecular vision, 2007, Jan-26, Volume: 13 Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Forkhead Box Protein L2; Forkhead Transcription Factors; Guanine; Heterozygote; Histidine; Humans; Mutation; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Serine; Syndrome; Thymine; Tyrosine	2007
Chemical and ultrastructural changes in tapetum of beagles with a hereditary abnormality. Investigative ophthalmology & visual science, 1982, Volume: 23, Issue:6 Topics: Animals; Choroid; Cysteine; Dogs; Eye; Eye Abnormalities; Histocytochemistry; Pigment Epithelium of Eye; Zinc	1982
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III. American journal of medical genetics, 1998, Jul-24, Volume: 78, Issue:4 Topics: Abnormalities, Multiple; Acrocephalosyndactylia; Amino Acid Substitution; Cysteine; Elbow; Eye Abnormalities; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infant, Newborn; Male; Phenotype; Point Mutation; Polymorphism, Single-Stranded Conformational; Radiography; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Serine; Translocation, Genetic; Wheelchairs	1998
Sprouty, an intracellular inhibitor of Ras signaling. Cell, 1999, Mar-05, Volume: 96, Issue:5 Topics: Animals; Cells, Cultured; Cysteine; Depression, Chemical; Drosophila melanogaster; Drosophila Proteins; ErbB Receptors; Eye; Eye Abnormalities; Eye Proteins; Insect Proteins; Macromolecular Substances; Membrane Glycoproteins; Membrane Proteins; Morphogenesis; Proteins; ras GTPase-Activating Proteins; ras Proteins; Receptor Protein-Tyrosine Kinases; Signal Transduction	1999
Mental deficiency and a new aminoaciduria. American journal of diseases of children (1960), 1969, Volume: 117, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Cysteine; Electrocardiography; Electroencephalography; Eye Abnormalities; Humans; Infections; Intellectual Disability; Intelligence Tests; Male; Middle Aged; Neurologic Examination; Radiography; Seizures; Sulfhydryl Compounds; Sulfides	1969