Page last updated: 2024-08-17

aspartic acid and Nanism

aspartic acid has been researched along with Nanism in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	1 (50.00)	2.80

Authors

Authors	Studies
Baker, RE; Basrai, MA; Corbett, AH; Enyenihi, L; Farchi, D; Fasken, MB; Hess, L; Kremsky, I; Lee, RS; Leung, SW; Sterrett, MC; Strassler, SE; van Hoof, A; Withers, ES	1
Chen, J; Li, G; Xu, C; Yang, J; Ying, H; Zhao, S	1

Other Studies

2 other study(ies) available for aspartic acid and Nanism

Article	Year
A budding yeast model for human disease mutations in the RNA (New York, N.Y.), 2021, Volume: 27, Issue:9 Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Multienzyme Ribonuclease Complex; Facies; Gene Expression; Glycine; Hearing Loss; Humans; Models, Biological; Models, Molecular; Mutation, Missense; Protein Conformation; Retinitis Pigmentosa; RNA-Binding Proteins; RNA, Fungal; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Syndrome	2021
Identification of a novel mutation in the FGFR3 gene in a Chinese family with Hypochondroplasia. Gene, 2018, Jan-30, Volume: 641 Topics: Adult; Asian People; Aspartic Acid; Bone and Bones; Child; Dwarfism; Exome; Glycine; Heterozygote; Humans; Limb Deformities, Congenital; Lordosis; Male; Mutation; Pathology, Molecular; Pedigree; Receptor, Fibroblast Growth Factor, Type 3	2018

Article

Year

A budding yeast model for human disease mutations in the

RNA (New York, N.Y.), 2021, Volume: 27, Issue:9

Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Multienzyme Ribonuclease Complex; Facies; Gene Expression; Glycine; Hearing Loss; Humans; Models, Biological; Models, Molecular; Mutation, Missense; Protein Conformation; Retinitis Pigmentosa; RNA-Binding Proteins; RNA, Fungal; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Syndrome

2021

Identification of a novel mutation in the FGFR3 gene in a Chinese family with Hypochondroplasia.

Gene, 2018, Jan-30, Volume: 641

Topics: Adult; Asian People; Aspartic Acid; Bone and Bones; Child; Dwarfism; Exome; Glycine; Heterozygote; Humans; Limb Deformities, Congenital; Lordosis; Male; Mutation; Pathology, Molecular; Pedigree; Receptor, Fibroblast Growth Factor, Type 3

2018