glycine has been researched along with Anhidrotic Ectodermal Dysplasia in 3 studies
Excerpt | Relevance | Reference |
---|---|---|
"hidrotic ectodermal dysplasia (HED) or Clouston syndrome is a rare autosomal dominant disorder affecting the skin and its derivatives." | 1.32 | A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia. ( Chen, JJ; Cui, Y; Dong, PL; He, PP; Huang, W; Li, YB; Wang, Y; Xiong, XY; Xu, SJ; Yang, S; Zhang, XJ; Zhou, Q, 2003) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Zhang, XJ | 1 |
Chen, JJ | 1 |
Yang, S | 1 |
Cui, Y | 1 |
Xiong, XY | 1 |
He, PP | 1 |
Dong, PL | 1 |
Xu, SJ | 1 |
Li, YB | 1 |
Zhou, Q | 1 |
Wang, Y | 1 |
Huang, W | 1 |
Lamartine, J | 1 |
Munhoz Essenfelder, G | 1 |
Kibar, Z | 1 |
Lanneluc, I | 1 |
Callouet, E | 1 |
Laoudj, D | 1 |
LemaƮtre, G | 1 |
Hand, C | 1 |
Hayflick, SJ | 1 |
Zonana, J | 1 |
Antonarakis, S | 1 |
Radhakrishna, U | 1 |
Kelsell, DP | 1 |
Christianson, AL | 1 |
Pitaval, A | 1 |
Der Kaloustian, V | 1 |
Fraser, C | 1 |
Blanchet-Bardon, C | 1 |
Rouleau, GA | 1 |
Waksman, G | 1 |
Tenenhouse, HS | 1 |
Gold, RJ | 1 |
3 other studies available for glycine and Anhidrotic Ectodermal Dysplasia
Article | Year |
---|---|
A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.
Topics: Adult; Amino Acid Substitution; Arginine; Asian People; Connexin 30; Connexins; Ectodermal Dysplasia | 2003 |
Mutations in GJB6 cause hidrotic ectodermal dysplasia.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Chromosome Mapping; Chromosomes, Hu | 2000 |
Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation.
Topics: Amino Acids; Animals; Chromatography, Gel; Ectodermal Dysplasia; Electrophoresis, Polyacrylamide Gel | 1976 |