proline has been researched along with Anhidrotic Ectodermal Dysplasia in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Jensen, JL; Lyngstadaas, SP; Nordgarden, H; Storhaug, K | 1 |
García-Díez, A; García-Rio, I; McLean, WH; Peñas, PF; Smith, FJ | 1 |
Camacho, J; Heymann, WR; Honig, PJ; Ilyas, E; Imaizumi, S; Li, W; Pawel, BR; Payne, AS; Schnur, RE; Seykora, JT; Yan, AC; Young, TL | 1 |
Coleman, CM; Del Monaco, M; McLean, WH; Morvay, M; Munro, CS; Rietveld, FJ; Smith, FJ; Steijlen, PM; Uitto, J | 1 |
Kucharska, D; Michalowski, R; Urban, J | 1 |
Gold, MB; Reynold, JM; Scriver, CR | 1 |
6 other study(ies) available for proline and Anhidrotic Ectodermal Dysplasia
Article | Year |
---|---|
Salivary gland function in persons with ectodermal dysplasias.
Topics: Adolescent; Adult; Aged; Case-Control Studies; Child; Child, Preschool; Ectodermal Dysplasia; Female; Humans; Male; Middle Aged; Parotid Gland; Peptides; Proline; Proline-Rich Protein Domains; Proteins; Saliva; Salivary Proteins and Peptides; Secretory Rate; Statistics, Nonparametric; Submandibular Gland | 2003 |
A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
Topics: Adult; Amino Acid Sequence; Ectodermal Dysplasia; Female; Humans; Keratins; Keratoderma, Palmoplantar; Keratosis; Mouth Diseases; Mutation, Missense; Nails, Malformed; Proline; Syndrome | 2005 |
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.
Topics: Abnormalities, Multiple; Arginine; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Genes, Tumor Suppressor; Genotype; Humans; Immunohistochemistry; Infant, Newborn; Male; Mutation, Missense; Phenotype; Phosphoproteins; Proline; Skin; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins | 2005 |
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1.
Topics: Cataract; Ectodermal Dysplasia; Female; Humans; Infant; Keratins; Male; Mutation, Missense; Nails, Malformed; Pedigree; Proline; Skin | 1999 |
[The Netherton syndrome with alopecia and prolinuria].
Topics: Alopecia; Ectodermal Dysplasia; Hair; Humans; Ichthyosis; Infant; Male; Proline; Renal Aminoacidurias; Scalp Dermatoses; Syndrome | 1978 |
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
Topics: Ectodermal Dysplasia; Genes, Dominant; Hair; Humans; Keratosis; Nails, Malformed; Phenylalanine; Proline; Serine; Sulfur; Tyrosine; Urea; Water | 1971 |