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ethylnitrosourea and Dental Enamel Hypoplasia

ethylnitrosourea has been researched along with Dental Enamel Hypoplasia in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adamson, SL; Anderson, N; Aubin, JE; Bai, D; Bruneau, BG; Ciliberti, N; Fleming, C; Flenniken, AM; Gittens, JE; Gong, XQ; Grynpas, M; Henderson, JE; Henkelman, RM; Kelsey, LB; Kidder, GM; Laird, DW; Lounsbury, C; McKerlie, C; Moreno, L; Nieman, BJ; Osborne, LR; Peterson, K; Qu, D; Roscoe, W; Rossant, J; Shao, Q; Sled, JG; Stanford, WL; Tong, D; Veitch, GI; Voronina, I; Vukobradovic, I; Wood, GA; Zhu, Y; Zirngibl, RA	1

Studies

Adamson, SL; Anderson, N; Aubin, JE; Bai, D; Bruneau, BG; Ciliberti, N; Fleming, C; Flenniken, AM; Gittens, JE; Gong, XQ; Grynpas, M; Henderson, JE; Henkelman, RM; Kelsey, LB; Kidder, GM; Laird, DW; Lounsbury, C; McKerlie, C; Moreno, L; Nieman, BJ; Osborne, LR; Peterson, K; Qu, D; Roscoe, W; Rossant, J; Shao, Q; Sled, JG; Stanford, WL; Tong, D; Veitch, GI; Voronina, I; Vukobradovic, I; Wood, GA; Zhu, Y; Zirngibl, RA

Other Studies

1 other study(ies) available for ethylnitrosourea and Dental Enamel Hypoplasia

Article	Year
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia. Development (Cambridge, England), 2005, Volume: 132, Issue:19 Topics: Abnormalities, Multiple; Animals; Biomechanical Phenomena; Bone and Bones; Bone Density; Connexin 43; Craniofacial Abnormalities; Dental Enamel Hypoplasia; Disease Models, Animal; Ethylnitrosourea; Eye Abnormalities; Gap Junctions; Heart Defects, Congenital; Humans; Mice; Penetrance; Point Mutation; Stem Cells; Syndactyly	2005

Article

Year

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.

Development (Cambridge, England), 2005, Volume: 132, Issue:19

Topics: Abnormalities, Multiple; Animals; Biomechanical Phenomena; Bone and Bones; Bone Density; Connexin 43; Craniofacial Abnormalities; Dental Enamel Hypoplasia; Disease Models, Animal; Ethylnitrosourea; Eye Abnormalities; Gap Junctions; Heart Defects, Congenital; Humans; Mice; Penetrance; Point Mutation; Stem Cells; Syndactyly

2005