tyrosine and 46, XY Gonadal Dysgenesis

tyrosine has been researched along with 46, XY Gonadal Dysgenesis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ben Gaied, D; Boujelben, S; Hizem, S; Kharrat, M; M'rad, R; Maazoul, F; Poulat, F; Tajouri, A	1
Frasier, SD; Jain, M; Jordan, BK; Natarajan, S; Vilain, E	1

Other Studies

2 other study(ies) available for tyrosine and 46, XY Gonadal Dysgenesis

Article	Year
Functional Analysis of Mutations at Codon 127 of the SRY Gene Associated with 46,XY Complete Gonadal Dysgenesis. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, 2017, Volume: 11, Issue:4 Topics: Adolescent; Base Sequence; Codon; DNA; DNA Mutational Analysis; Female; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; HEK293 Cells; Humans; Mutation; Nuclear Localization Signals; Sex-Determining Region Y Protein; Tyrosine	2017
Familial mutation in the testis-determining gene SRY shared by an XY female and her normal father. The Journal of clinical endocrinology and metabolism, 2002, Volume: 87, Issue:7 Topics: Amino Acid Substitution; Base Sequence; DNA-Binding Proteins; Fathers; Female; Genes, sry; Gonadal Dysgenesis, 46,XY; HMG-Box Domains; Humans; Male; Mutation; Nuclear Proteins; Phenylalanine; Polymerase Chain Reaction; Reference Values; Sex-Determining Region Y Protein; Testis; Transcription Factors; Tyrosine	2002

Article

Year

Functional Analysis of Mutations at Codon 127 of the SRY Gene Associated with 46,XY Complete Gonadal Dysgenesis.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, 2017, Volume: 11, Issue:4

Topics: Adolescent; Base Sequence; Codon; DNA; DNA Mutational Analysis; Female; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; HEK293 Cells; Humans; Mutation; Nuclear Localization Signals; Sex-Determining Region Y Protein; Tyrosine

2017

Familial mutation in the testis-determining gene SRY shared by an XY female and her normal father.

The Journal of clinical endocrinology and metabolism, 2002, Volume: 87, Issue:7

Topics: Amino Acid Substitution; Base Sequence; DNA-Binding Proteins; Fathers; Female; Genes, sry; Gonadal Dysgenesis, 46,XY; HMG-Box Domains; Humans; Male; Mutation; Nuclear Proteins; Phenylalanine; Polymerase Chain Reaction; Reference Values; Sex-Determining Region Y Protein; Testis; Transcription Factors; Tyrosine

2002