tyrosine and Chondrodystrophic Myotonia

tyrosine has been researched along with Chondrodystrophic Myotonia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Costa, T; Erlacher, L; Kilpatrick, MW; Lembessis, P; Lin, K; Luyten, FP; Thomas, JT; Tsipouras, P	1
Ida, A; Koyama, K; Nakata, Y; Sawai, H	1

Other Studies

2 other study(ies) available for tyrosine and Chondrodystrophic Myotonia

Article	Year
Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1. Nature genetics, 1997, Volume: 17, Issue:1 Topics: Amino Acid Sequence; Animals; Base Sequence; Bone Morphogenetic Proteins; Conserved Sequence; COS Cells; Cysteine; Dwarfism; Female; Fingers; Genes, Dominant; Genes, Recessive; Growth Differentiation Factor 5; Growth Substances; Hand Deformities, Congenital; Heterozygote; Humans; Male; Morphogenesis; Osteochondrodysplasias; Pedigree; Point Mutation; Recombinant Proteins; Transfection; Tyrosine	1997
Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasia. Journal of human genetics, 1998, Volume: 43, Issue:4 Topics: Adult; Amino Acid Substitution; Codon; Collagen; Cysteine; DNA; DNA Mutational Analysis; Female; Humans; Mutation, Missense; Osteochondrodysplasias; Pedigree; Polymerase Chain Reaction; Tyrosine	1998

Article

Year

Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1.

Nature genetics, 1997, Volume: 17, Issue:1

Topics: Amino Acid Sequence; Animals; Base Sequence; Bone Morphogenetic Proteins; Conserved Sequence; COS Cells; Cysteine; Dwarfism; Female; Fingers; Genes, Dominant; Genes, Recessive; Growth Differentiation Factor 5; Growth Substances; Hand Deformities, Congenital; Heterozygote; Humans; Male; Morphogenesis; Osteochondrodysplasias; Pedigree; Point Mutation; Recombinant Proteins; Transfection; Tyrosine

1997

Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasia.

Journal of human genetics, 1998, Volume: 43, Issue:4

Topics: Adult; Amino Acid Substitution; Codon; Collagen; Cysteine; DNA; DNA Mutational Analysis; Female; Humans; Mutation, Missense; Osteochondrodysplasias; Pedigree; Polymerase Chain Reaction; Tyrosine

1998