glutamine and Anhidrotic Ectodermal Dysplasia

glutamine 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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Calabrò, V; Calogero, RA; Crispi, S; Di Costanzo, A; La Mantia, G; Lo Iacono, M; Mansueto, G; Pollice, A; Saviozzi, S	1
Adès, LC; Gilmour, E; Graf, N; Holme, SA; Maclean, K; Moss, C; Onikul, E; Scheffer, H; Smith, GH; Taylor, M; van Bokhoven, H	1

Other Studies

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

Article	Year
The Hay Wells syndrome-derived TAp63alphaQ540L mutant has impaired transcriptional and cell growth regulatory activity. Cell cycle (Georgetown, Tex.), 2006, Volume: 5, Issue:1 Topics: Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; DNA-Binding Proteins; Ectodermal Dysplasia; Gene Expression Profiling; Gene Expression Regulation; Genes, Tumor Suppressor; Glutamine; Humans; Mutation; Phosphoproteins; Promoter Regions, Genetic; Protein Isoforms; Proto-Oncogene Proteins c-mdm2; Trans-Activators; Transcription Factors; Transcription, Genetic; Tumor Suppressor Proteins	2006
EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation? American journal of medical genetics. Part A, 2007, May-15, Volume: 143A, Issue:10 Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders	2007

Article

Year

The Hay Wells syndrome-derived TAp63alphaQ540L mutant has impaired transcriptional and cell growth regulatory activity.

Cell cycle (Georgetown, Tex.), 2006, Volume: 5, Issue:1

Topics: Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; DNA-Binding Proteins; Ectodermal Dysplasia; Gene Expression Profiling; Gene Expression Regulation; Genes, Tumor Suppressor; Glutamine; Humans; Mutation; Phosphoproteins; Promoter Regions, Genetic; Protein Isoforms; Proto-Oncogene Proteins c-mdm2; Trans-Activators; Transcription Factors; Transcription, Genetic; Tumor Suppressor Proteins

2006

EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?

American journal of medical genetics. Part A, 2007, May-15, Volume: 143A, Issue:10

Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders

2007