isoleucine and Anhidrotic Ectodermal Dysplasia

isoleucine has been researched along with Anhidrotic Ectodermal Dysplasia 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	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cheng, K; Li, W; Liu, S; Luo, L; Ring, BZ; Su, L; Tang, Z; Wang, J; Wang, M; Xu, J; Xue, W; Yang, Y; Zhu, P	1
Baal, C; Hemmer, W; Jarisch, R; Litschauer-Poursadrollah, M; Mayer, DE	1

Other Studies

2 other study(ies) available for isoleucine and Anhidrotic Ectodermal Dysplasia

Article	Year
Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia. Journal of dental research, 2013, Volume: 92, Issue:6 Topics: Adolescent; Anodontia; Conserved Sequence; Cuspid; Ectodermal Dysplasia; Ectodysplasins; Exons; Female; Guanine; Humans; Incisor; Isoleucine; Leucine; Male; MSX1 Transcription Factor; Mutation, Missense; PAX9 Transcription Factor; Pedigree; Phenotype; Sequence Homology, Amino Acid; Serine; Structural Homology, Protein; Thymine; Tumor Necrosis Factors; Valine	2013
Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2010, Volume: 8, Issue:2 Topics: Amino Acid Substitution; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Dental Enamel Hypoplasia; Dental Pulp Cavity; Dermatitis, Atopic; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Genes, Dominant; Hair; Homeodomain Proteins; Humans; Isoleucine; Microscopy, Electron; Phenotype; Serine; Syndrome; Tooth Abnormalities; Transcription Factors	2010

Article

Year

Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.

Journal of dental research, 2013, Volume: 92, Issue:6

Topics: Adolescent; Anodontia; Conserved Sequence; Cuspid; Ectodermal Dysplasia; Ectodysplasins; Exons; Female; Guanine; Humans; Incisor; Isoleucine; Leucine; Male; MSX1 Transcription Factor; Mutation, Missense; PAX9 Transcription Factor; Pedigree; Phenotype; Sequence Homology, Amino Acid; Serine; Structural Homology, Protein; Thymine; Tumor Necrosis Factors; Valine

2013

Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2010, Volume: 8, Issue:2

Topics: Amino Acid Substitution; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Dental Enamel Hypoplasia; Dental Pulp Cavity; Dermatitis, Atopic; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Genes, Dominant; Hair; Homeodomain Proteins; Humans; Isoleucine; Microscopy, Electron; Phenotype; Serine; Syndrome; Tooth Abnormalities; Transcription Factors

2010