Compounds > arginine

arginine and Microphthalmia

arginine has been researched along with Microphthalmia in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (33.33)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Frei, E; Frei, K; Frohne, A; Koenighofer, M; Lucas, T; Mitulovic, G; Parzefall, T; Schoefer, C; Waldstein, SM	1
Nakamura, T; Pichel, JG; Westphal, H; Williams-Simons, L	1
Chang, B; Davisson, MT; Gong, X; Hawes, NL; Lo, WK; Ojakian, R; Wang, X	1

Other Studies

3 other study(ies) available for arginine and Microphthalmia

Article	Year
A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity. Experimental eye research, 2021, Volume: 205 Topics: Adult; Aged, 80 and over; Amino Acid Substitution; Arginine; Exome Sequencing; Female; Filtering Surgery; Glaucoma, Angle-Closure; Humans; Hyperopia; Lens Implantation, Intraocular; Male; Membrane Proteins; Microphthalmos; Microscopy, Acoustic; Middle Aged; Mutation, Missense; Pedigree; Phacoemulsification; Proline; Protein Conformation, alpha-Helical; Slit Lamp Microscopy; Vision Disorders; Visual Acuity	2021
An apoptotic defect in lens differentiation caused by human p53 is rescued by a mutant allele. Proceedings of the National Academy of Sciences of the United States of America, 1995, Jun-20, Volume: 92, Issue:13 Topics: Aging; Alanine; Alleles; Animals; Apoptosis; Arginine; Cell Differentiation; Codon; Epithelial Cells; Gene Expression; Genes, p53; Genetic Therapy; Humans; Lens, Crystalline; Mice; Mice, Transgenic; Microphthalmos; Point Mutation; Proline; Tumor Suppressor Protein p53; Valine	1995
A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice. Human molecular genetics, 2002, Mar-01, Volume: 11, Issue:5 Topics: Amino Acid Substitution; Animals; Arginine; Base Sequence; Cataract; Chromosome Mapping; Codon; Connexins; Crosses, Genetic; Eye Proteins; Female; Genes, Dominant; Genetic Linkage; Genetic Markers; Genotype; Lens, Crystalline; Male; Mice; Mice, Inbred AKR; Mice, Inbred BALB C; Microphthalmos; Pedigree; Phenotype; Point Mutation; Sequence Analysis, DNA	2002