valine and Cataract

valine has been researched along with Cataract in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19901 (10.00)18.7374
1990's1 (10.00)18.2507
2000's3 (30.00)29.6817
2010's5 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bharat, SV; Pande, J; Shekhtman, A1
Ikeda, S; Kato, T; Koyama, S; Maruyama, K; Sekijima, Y; Yoshida, T; Yoshinaga, T1
Hu, S; Ma, X; Qi, Y; Wang, B; Zhou, N; Zhou, S; Zhou, Z1
Ramaiya, KJ; Rao, PK1
Jin, C; Li, J; Shentu, X; Wang, Q; Wang, W; Yao, K; Zhu, Y1
Ikeda, S; Mitsuhashi, S; Tokuda, T; Yamamoto, K; Yazaki, M1
Hennies, HC; Nürnberg, P; Singh, D; Singh, JR; Sperling, K; Vanita, V1
Engel, W; Graw, J; Illig, T; Klopp, N; Pauli, S; Söker, T1
Dean, RT; Fu, SL1
Gruber, L; Harris, JE1

Other Studies

10 other study(ies) available for valine and Cataract

ArticleYear
The cataract-associated V41M mutant of human γS-crystallin shows specific structural changes that directly enhance local surface hydrophobicity.
    Biochemical and biophysical research communications, 2014, Jan-03, Volume: 443, Issue:1

    Topics: Amides; Amino Acid Substitution; Cataract; gamma-Crystallins; Humans; Hydrophobic and Hydrophilic Interactions; Methionine; Mutation; Nuclear Magnetic Resonance, Biomolecular; Protein Structure, Tertiary; Valine

2014
Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene.
    Internal medicine (Tokyo, Japan), 2014, Volume: 53, Issue:23

    Topics: Achilles Tendon; Alanine; Ataxia; Brain; Cataract; Chenodeoxycholic Acid; Cholestanetriol 26-Monooxygenase; Cholestanol; Deglutition Disorders; Dysarthria; Dystonia; Early Diagnosis; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Middle Aged; Muscle Spasticity; Muscle Weakness; Mutation; Pedigree; Radiography; Treatment Outcome; Valine; Xanthomatosis, Cerebrotendinous

2014
Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3).
    Molecular vision, 2010, Apr-21, Volume: 16

    Topics: Adenine; Adult; Asian People; Cataract; Child, Preschool; Connexins; DNA Mutational Analysis; Female; Guanine; Humans; Male; Methionine; Mutation, Missense; Pedigree; Valine

2010
Herpetic necrotizing retinitis following flucinolone acetonide intravitreal implant.
    Ocular immunology and inflammation, 2011, Volume: 19, Issue:1

    Topics: Acyclovir; Antiviral Agents; Azathioprine; Cataract; Drug Implants; Eye Infections, Viral; Herpes Simplex; Herpesvirus 2, Human; Humans; Immunosuppressive Agents; Male; Mycophenolic Acid; Panuveitis; Pregnadienetriols; Retinal Necrosis Syndrome, Acute; Treatment Outcome; Valacyclovir; Valine; Visual Acuity; Young Adult

2011
Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family.
    Molecular vision, 2011, Jan-13, Volume: 17

    Topics: Alanine; beta-Crystallin B Chain; Cataract; China; DNA Mutational Analysis; Female; Humans; Male; Mutation; Pedigree; Phenotype; Polymorphism, Restriction Fragment Length; Valine

2011
MRI analysis on a patient with the V30M mutation is characteristic of leptomeningeal amyloid.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2004, Volume: 11, Issue:4

    Topics: Amino Acid Substitution; Amyloid Neuropathies; Brain; Cataract; Gadolinium; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Point Mutation; Prealbumin; Radiography; Spinal Cord; Valine

2004
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
    Molecular vision, 2006, Oct-18, Volume: 12

    Topics: Asian People; Base Sequence; Cataract; Child; Connexins; Cytosine; DNA Mutational Analysis; Eye Proteins; Female; Genes, Dominant; Genetic Linkage; Genotype; Guanine; Haplotypes; Heterozygote; Humans; India; Leucine; Male; Molecular Sequence Data; Mutation; Phenotype; Protein Structure, Tertiary; Transcription Initiation Site; Valine

2006
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.
    Molecular vision, 2007, Jun-19, Volume: 13

    Topics: Alleles; Amino Acid Sequence; Aspartic Acid; Base Sequence; beta-Crystallin B Chain; Cataract; Child, Preschool; DNA Mutational Analysis; Female; Germany; Humans; Infant, Newborn; Male; Molecular Biology; Molecular Sequence Data; Mutation; Pedigree; Proteomics; Valine

2007
Structural characterization of the products of hydroxyl-radical damage to leucine and their detection on proteins.
    The Biochemical journal, 1997, May-15, Volume: 324 ( Pt 1)

    Topics: Cataract; Chromatography, High Pressure Liquid; Crystallins; Humans; Hydroxyl Radical; Indicators and Reagents; Lens, Crystalline; Leucine; Lipoproteins; o-Phthalaldehyde; Oligopeptides; Oxidation-Reduction; Proline; Schiff Bases; Valine

1997
The reversal of triparanol-induced cataracts in the rat. 3. Amino acid content and uptake of 14 C -AIB in cataractous and clearing lenses.
    Investigative ophthalmology, 1973, Volume: 12, Issue:5

    Topics: Alanine; Amino Acids; Aminoisobutyric Acids; Animals; Arginine; Aspartic Acid; Carbon Isotopes; Cataract; Cystine; Diet; Glutamates; Glycine; Histidine; Isoleucine; Lens, Crystalline; Leucine; Lysine; Methionine; Phenylalanine; Proline; Rats; Serine; Threonine; Triparanol; Tyrosine; Valine

1973