serine has been researched along with Anhidrotic Ectodermal Dysplasia in 5 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "He does not display features of ectodermal dysplasia and did not suffer from serious infections with the exception of a relapsing Salmonella typhimurium infection." | 1.32 | The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes. ( Bredius, R; Hoeve, MA; Janssen, R; Lankester, A; Ottenhoff, TH; ten Dam, M; van de Vosse, E; van der Burg, M; van Dissel, JT; van Dongen, J; van Tol, M; van Wengen, A; Weemaes, C, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yang, Y | 1 |
| Luo, L | 1 |
| Xu, J | 1 |
| Zhu, P | 1 |
| Xue, W | 1 |
| Wang, J | 1 |
| Li, W | 1 |
| Wang, M | 1 |
| Cheng, K | 1 |
| Liu, S | 1 |
| Tang, Z | 1 |
| Ring, BZ | 1 |
| Su, L | 1 |
| Mayer, DE | 1 |
| Baal, C | 1 |
| Litschauer-Poursadrollah, M | 1 |
| Hemmer, W | 1 |
| Jarisch, R | 1 |
| Janssen, R | 1 |
| van Wengen, A | 1 |
| Hoeve, MA | 1 |
| ten Dam, M | 1 |
| van der Burg, M | 1 |
| van Dongen, J | 1 |
| van de Vosse, E | 1 |
| van Tol, M | 1 |
| Bredius, R | 1 |
| Ottenhoff, TH | 1 |
| Weemaes, C | 1 |
| van Dissel, JT | 1 |
| Lankester, A | 1 |
| Aoki, N | 1 |
| Ito, K | 1 |
| Tachibana, T | 1 |
| Ito, M | 1 |
| Reynold, JM | 1 |
| Gold, MB | 1 |
| Scriver, CR | 1 |
5 other studies available for serine and Anhidrotic Ectodermal Dysplasia
| Article | Year |
|---|---|
Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.
Topics: Adolescent; Anodontia; Conserved Sequence; Cuspid; Ectodermal Dysplasia; Ectodysplasins; Exons; Fema | 2013 |
Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.
Topics: Amino Acid Substitution; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Dental Enamel H | 2010 |
The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes.
Topics: Active Transport, Cell Nucleus; Adult; Alleles; B-Lymphocytes; Cell Division; Cell Nucleus; Child, P | 2004 |
A novel arginine-->Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia.
Topics: Amino Acid Substitution; Arginine; Asian People; Child, Preschool; Ectodermal Dysplasia; Genetic Lin | 2000 |
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
Topics: Ectodermal Dysplasia; Genes, Dominant; Hair; Humans; Keratosis; Nails, Malformed; Phenylalanine; Pro | 1971 |