Page last updated: 2024-10-18

glycine and Anodontia

glycine has been researched along with Anodontia in 4 studies

Anodontia: Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bailleul-Forestier, I1
Gros, C1
Zenaty, D1
Bennaceur, S1
Leger, J1
de Roux, N1
Boeira, BR1
Echeverrigaray, S1
Item, CB1
Turhani, D1
Thurnher, D1
Yerit, K1
Sinko, K1
Wittwer, G1
Adeyemo, WL1
Frei, K1
Erginel-Unaltuna, N1
Watzinger, F1
Ewers, R1
Tarpey, P1
Pemberton, TJ1
Stockton, DW1
Das, P1
Ninis, V1
Edkins, S1
Andrew Futreal, P1
Wooster, R1
Kamath, S1
Nayak, R1
Stratton, MR1
Patel, PI1

Other Studies

4 other studies available for glycine and Anodontia

ArticleYear
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
    International journal of paediatric dentistry, 2010, Volume: 20, Issue:4

    Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine;

2010
Novel missense mutation in PAX9 gene associated with familial tooth agenesis.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2013, Volume: 42, Issue:1

    Topics: Alanine; Amino Acid Substitution; Anodontia; Genes, Dominant; Glycine; Humans; Mutation, Missense; P

2013
Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
    International journal of molecular medicine, 2005, Volume: 15, Issue:2

    Topics: 5' Untranslated Regions; Abnormalities, Multiple; Anodontia; Arginine; Base Sequence; Cleft Lip; Cle

2005
A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia.
    American journal of medical genetics. Part A, 2007, Feb-15, Volume: 143, Issue:4

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Anodontia; Base Sequence; Ectodysplasins; Gen

2007