Compounds > proline

proline and Anhidrotic Ectodermal Dysplasia

proline has been researched along with Anhidrotic Ectodermal Dysplasia in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jensen, JL; Lyngstadaas, SP; Nordgarden, H; Storhaug, K1
García-Díez, A; García-Rio, I; McLean, WH; Peñas, PF; Smith, FJ1
Camacho, J; Heymann, WR; Honig, PJ; Ilyas, E; Imaizumi, S; Li, W; Pawel, BR; Payne, AS; Schnur, RE; Seykora, JT; Yan, AC; Young, TL1
Coleman, CM; Del Monaco, M; McLean, WH; Morvay, M; Munro, CS; Rietveld, FJ; Smith, FJ; Steijlen, PM; Uitto, J1
Kucharska, D; Michalowski, R; Urban, J1
Gold, MB; Reynold, JM; Scriver, CR1

Other Studies

6 other study(ies) available for proline and Anhidrotic Ectodermal Dysplasia

ArticleYear
Salivary gland function in persons with ectodermal dysplasias.
    European journal of oral sciences, 2003, Volume: 111, Issue:5

    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.
    The British journal of dermatology, 2005, Volume: 152, Issue:4

    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.
    Archives of dermatology, 2005, Volume: 141, Issue:12

    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.
    The British journal of dermatology, 1999, Volume: 141, Issue:6

    Topics: Cataract; Ectodermal Dysplasia; Female; Humans; Infant; Keratins; Male; Mutation, Missense; Nails, Malformed; Pedigree; Proline; Skin

1999
[The Netherton syndrome with alopecia and prolinuria].
    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1978, Volume: 29, Issue:4

    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.
    Birth defects original article series, 1971, Volume: 7, Issue:8

    Topics: Ectodermal Dysplasia; Genes, Dominant; Hair; Humans; Keratosis; Nails, Malformed; Phenylalanine; Proline; Serine; Sulfur; Tyrosine; Urea; Water

1971