arginine and 46, XY Gonadal Dysgenesis

arginine has been researched along with 46, XY Gonadal Dysgenesis in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Chen, Y; Han, B; Liu, J; Liu, Y; Qiao, J; Song, H; Wang, H; Wang, N; Zhao, S; Zhu, H; Zhu, W1
Jyothy, A; Sharma, V; Singh, R; Thangaraj, K1
Büttner, HH; Kunkel, S; Meissner, J; Pelz, L; Rudolf, K1
Angeletti, B; Battiloro, E; Bruni, L; D'Ambrosio, E; Tondini, S; Tozzi, MC; Verna, R; Vignetti, P1

Other Studies

4 other study(ies) available for arginine and 46, XY Gonadal Dysgenesis

ArticleYear
Inherited Missense Mutation Occurring in Arginine76 of the SRY Gene Does Not Account for Familial 46, XY Sex Reversal.
    The Journal of clinical endocrinology and metabolism, 2020, 05-01, Volume: 105, Issue:5

    Topics: Adult; Arginine; Family; Female; Gonadal Dysgenesis, 46,XY; Humans; Inheritance Patterns; Male; Middle Aged; Mutation, Missense; Pedigree; Sex-Determining Region Y Protein; Young Adult

2020
A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.
    Fertility and sterility, 2011, Volume: 95, Issue:2

    Topics: Adolescent; Amino Acid Substitution; Androgen-Insensitivity Syndrome; Arginine; Base Sequence; Child; DNA; Female; Gonadal Dysgenesis, 46,XY; Hernia, Inguinal; Humans; Male; Mutation, Missense; Pedigree; Protein Interaction Domains and Motifs; Receptors, Androgen; Serine; Siblings

2011
[Behavior of the hypothalamo-hypophyseal axis in a patient with asymmetric mixed gonadal dysgenesis (chromosome pattern 45,XO/46,XY) before and after gonad excision after with arginine, GRH and TRH stimulation].
    Endokrinologie, 1982, Volume: 79, Issue:3

    Topics: Arginine; Child; Chlormadinone Acetate; Female; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; Gonadotropin-Releasing Hormone; Humans; Hypothalamo-Hypophyseal System; Mestranol; Thyrotropin-Releasing Hormone

1982
A novel double nucleotide substitution in the HMG box of the SRY gene associated with Swyer syndrome.
    Human genetics, 1997, Volume: 100, Issue:5-6

    Topics: Adult; Arginine; Asparagine; Base Sequence; Deoxyribonucleases, Type II Site-Specific; DNA Mutational Analysis; DNA-Binding Proteins; Female; Genes; Gonadal Dysgenesis, 46,XY; High Mobility Group Proteins; Humans; Mutation; Nuclear Proteins; Sex-Determining Region Y Protein; Transcription Factors

1997