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histidine and Disorders of Sex Development

histidine has been researched along with Disorders of Sex Development in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boudon, C; Garandeau, P; Lobaccaro, JM; Lumbroso, S; Montoya, P; Romer, TE; Sultan, C; Szarras-Czapnik, M1
de Zegher, F; Deloof, E; Devlieger, H; Devriendt, K; Legius, E; Moerman, P; Proesmans, W; Vanhole, C1
Amram, S; Belon, C; Bringer, J; Lobaccaro, JM; Lumbroso, S; Rodier, M; Sultan, C1
Belsham, DD; Bordet, S; Greenberg, C; Kaufman, M; Mhatre, A; Pereira, F; Pinsky, L; Prior, L; Trifiro, MA; Wrogeman, K1

Other Studies

4 other study(ies) available for histidine and Disorders of Sex Development

ArticleYear
Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiency.
    The Journal of clinical endocrinology and metabolism, 1995, Volume: 80, Issue:7

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Adolescent; Amino Acid Sequence; Arginine; Asparagine; Base Sequence; Disorders of Sex Development; Exons; Female; France; Glutamine; Histidine; Humans; Introns; Male; Molecular Sequence Data; Open Reading Frames; Point Mutation; Poland; Serine

1995
Diaphragmatic hernia in Denys-Drash syndrome.
    American journal of medical genetics, 1995, May-22, Volume: 57, Issue:1

    Topics: Animals; Arginine; Base Sequence; Chromosomes, Human, Pair 11; Disorders of Sex Development; DNA-Binding Proteins; Exons; Female; Gene Deletion; Genes, Tumor Suppressor; Gonadal Dysgenesis; Hernia, Diaphragmatic; Heterozygote; Histidine; Homozygote; Humans; Infant, Newborn; Kidney Glomerulus; Mice; Mice, Transgenic; Molecular Sequence Data; Ovary; Point Mutation; Syndrome; Transcription Factors; WT1 Proteins

1995
[Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1993, Volume: 187, Issue:4

    Topics: Arginine; Disorders of Sex Development; Exons; Histidine; Humans; Male; Mutation; Receptors, Androgen; Syndrome

1993
Replacement of arginine 773 by cysteine or histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes.
    American journal of human genetics, 1992, Volume: 51, Issue:1

    Topics: Adolescent; Arginine; Base Sequence; Canada; Cysteine; Deoxyribonucleases, Type II Site-Specific; Disorders of Sex Development; Female; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polymerase Chain Reaction; Receptors, Androgen; Transcriptional Activation

1992