Compounds > cysteine

cysteine and Ectopia Lentis

cysteine has been researched along with Ectopia Lentis in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (40.00)	29.6817
2010's	3 (60.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Breuning, MH; Cobben, JM; Giroth, C; Hamel, BC; Hansson, KB; Hilhorst-Hofstee, Y; Mancini, GM; Moll, HA; Pals, G; Rijlaarsdam, ME; Ruivenkamp, CA; Timmermans, J; Verheij, JB	1
Fan, W; Liang, C; Liu, Y; Wu, S	1
Chu, M; Yang, G; Zhai, X; Zhao, J	1
Jiang, J; Jin, C; Shentu, X; Tang, X; Wu, R; Yao, K	1
Robinson, PN; Singh, D; Singh, JR; Sperling, K; Vanita, V; Varon, R	1

Other Studies

5 other study(ies) available for cysteine and Ectopia Lentis

Article	Year
The clinical spectrum of complete FBN1 allele deletions. European journal of human genetics : EJHG, 2011, Volume: 19, Issue:3 Topics: Adolescent; Adult; Alleles; Child; Child, Preschool; Cysteine; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Haploinsufficiency; Humans; Male; Marfan Syndrome; Microfilament Proteins; Mitral Valve Prolapse; Mutation; Phenotype; Sequence Deletion; Young Adult	2011
Identification of a novel FBN1 mutation in a Chinese family with isolated ectopia lentis. Molecular vision, 2011, Volume: 17 Topics: Adult; Aged; Amino Acid Substitution; Arginine; Asian People; Base Sequence; Cysteine; DNA Mutational Analysis; Ectopia Lentis; Exons; Female; Fibrillin-1; Fibrillins; Genes, Dominant; Humans; Lens, Crystalline; Male; Marfan Syndrome; Microfilament Proteins; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation	2011
A novel FBN1 mutation in a Chinese family with isolated ectopia lentis. Molecular vision, 2012, Volume: 18 Topics: Adolescent; Adult; Animals; Arginine; Asian People; Base Sequence; Case-Control Studies; Cysteine; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Genes, Dominant; Haplotypes; Humans; Lens, Crystalline; Male; Microfilament Proteins; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Sequence Alignment; Sequence Analysis, DNA	2012
Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients. Molecular vision, 2007, Jul-24, Volume: 13 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Asian People; Base Sequence; Child; Cysteine; DNA Mutational Analysis; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Genetic Predisposition to Disease; Humans; Male; Marfan Syndrome; Microfilament Proteins; Molecular Sequence Data; Mutation; Pedigree	2007
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin. Molecular vision, 2007, Oct-25, Volume: 13 Topics: Adult; Amino Acid Substitution; Arginine; Child; Codon; Cysteine; Cytosine; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Genes, Dominant; Genetic Linkage; Genotype; Haplotypes; Heterozygote; Humans; India; Lod Score; Male; Microfilament Proteins; Middle Aged; Mutation; Pedigree; Thymine	2007