threonine and 46, XY Gonadal Dysgenesis

threonine has been researched along with 46, XY Gonadal Dysgenesis in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
He, F; Li, C; Li, X; Wang, X; Xue, M; Zhao, M1

Other Studies

1 other study(ies) available for threonine and 46, XY Gonadal Dysgenesis

ArticleYear
Identification of a novel mutation (Ala66Thr) of SRY gene causes XY pure gonadal dysgenesis by affecting DNA binding activity and nuclear import.
    Gene, 2018, Apr-20, Volume: 651

    Topics: Active Transport, Cell Nucleus; Adolescent; Adult; Alanine; DNA; Female; Gonadal Dysgenesis, 46,XY; HEK293 Cells; Humans; Karyotyping; Male; Mutation, Missense; Protein Binding; Protein Conformation; Sequence Analysis, DNA; Sex-Determining Region Y Protein; Threonine; Young Adult

2018