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Page last updated: 2024-08-17

lysine and Acanthosis Nigricans

lysine has been researched along with Acanthosis Nigricans in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alonso, A; Alvarez, A; Barreiro, J; Cabanas, P; Castro-Feijóo, L; Domínguez, F; Loidi, L; Parajes, S; Pombo, M; Rosón, E; Vidal, A1
Buckley, MF; Elakis, G; Gardener, G; Inglis, G; Roscioli, T; Susman, RD; Zankl, A1
Bamshad, MJ; Bellus, GA; Curry, CJ; Dorst, J; Francomano, CA; Hurko, O; Jabs, EW; Lachman, RS; Lee, RR; Przylepa, KA; Rimoin, DL; Wilcox, WR1

Other Studies

3 other study(ies) available for lysine and Acanthosis Nigricans

ArticleYear
Hypochondroplasia and Acanthosis nigricans: a new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?
    European journal of endocrinology, 2008, Volume: 159, Issue:3

    Topics: Acanthosis Nigricans; Adolescent; Amino Acid Substitution; Base Sequence; Body Height; DNA Mutational Analysis; Humans; Lysine; Male; Mutation, Missense; Osteochondrodysplasias; Pedigree; Polymorphism, Single Nucleotide; Receptor, Fibroblast Growth Factor, Type 3; Syndrome; Threonine

2008
Prenatal and postnatal presentation of severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) due to the FGFR3 Lys650Met mutation.
    American journal of medical genetics. Part A, 2008, Jan-15, Volume: 146A, Issue:2

    Topics: Acanthosis Nigricans; Achondroplasia; Amino Acid Substitution; Developmental Disabilities; Female; Fetus; Humans; Infant, Newborn; Lysine; Male; Methionine; Mutation, Missense; Pregnancy; Receptor, Fibroblast Growth Factor, Type 3; Ultrasonography, Prenatal

2008
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3.
    American journal of medical genetics, 1999, Jul-02, Volume: 85, Issue:1

    Topics: Acanthosis Nigricans; Developmental Disabilities; Female; Humans; Infant, Newborn; Lysine; Male; Methionine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Skull

1999