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Collection of 2429 constrained headshots of 277 volunteers for deep learning.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07560-2
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- Article
Clinical and molecular studies in four patients with SRY-positive 46,XX testicular disorders of sex development: implications for variable sex development and genomic rearrangements.
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- Journal of Human Genetics, 2014, v. 59, n. 10, p. 549, doi. 10.1038/jhg.2014.70
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- Article
The p.R92W variant of NR5A1/Nr5a1 induces testicular development of 46,XX gonads in humans, but not in mice: phenotypic comparison of human patients and mutation-induced mice.
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- Biology of Sex Differences, 2016, v. 7, p. 1, doi. 10.1186/s13293-016-0114-6
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- Article
Enhancement of lung carcinogenesis initiated with 4-(N-hydroxymethylnitrosamino)-1-(3-pyridyl)-1-butanone by Ogg1 gene deficiency in female, but not male,mice.
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- Journal of Toxicological Sciences, 2009, v. 34, n. 2, p. 163, doi. 10.2131/jts.34.163
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- Article
Cryptic Genomic Rearrangements in Three Patients with 46,XY Disorders of Sex Development.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068194
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- Article
Dietary supplement use in elementary school children: a Japanese web-based survey.
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- Environmental Health & Preventive Medicine, 2021, v. 26, n. 1, p. 1, doi. 10.1186/s12199-021-00985-7
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- Article
Involvement of Mutation-based Inhibition of β-Catenin Phosphorylation at Ser33 in the Malignant Progression of Lung (Pre)neoplastic Lesions Induced by N-nitrosobis(2-hydroxypropyl)amine in Male Fischer 344 Rats.
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- Lung, 2007, v. 185, n. 5, p. 271, doi. 10.1007/s00408-007-9017-y
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- Article
A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1.
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- Sexual Development, 2019, v. 13, n. 2, p. 60, doi. 10.1159/000496777
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- Article
Phenotypic Variation in 46,XX Disorders of Sex Development due to the <bold><italic>NR5A1 </italic></bold>p.R92W Variant: A Sibling Case Report and Literature Review.
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- Sexual Development, 2017, v. 11, n. 5/6, p. 284, doi. 10.1159/000485868
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- Article
Copy Number Variations of the Azoospermia Factor Region and SRY Are Not Associated with the Risk of Hypospadias.
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- Sexual Development, 2016, v. 10, n. 1, p. 12, doi. 10.1159/000444938
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- Article
SOX3 Overdosage Permits Normal Sex Development in Females with Random X Inactivation.
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- Sexual Development, 2015, v. 9, n. 3, p. 125, doi. 10.1159/000377653
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- Article
Novel Splice Site Mutation in MAMLD1 in a Patient with Hypospadias.
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- Sexual Development, 2015, v. 9, n. 3, p. 130, doi. 10.1159/000380842
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- Article
GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population.
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- BMC Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12863-019-0763-7
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- Article
Sodium phenylacetate inhibits the Ras/MAPK signaling pathway to induce reduction of the c-Raf-1 protein in human and canine breast cancer cells.
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- Breast Cancer Research & Treatment, 2010, v. 118, n. 2, p. 281, doi. 10.1007/s10549-008-0215-y
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- Article
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.
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- Journal of Cellular & Molecular Medicine, 2017, v. 21, n. 10, p. 2623, doi. 10.1111/jcmm.13146
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- Article
Methylation of neutral endopeptidase 24.11 promoter in rat hepatocellular carcinoma.
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- Cancer Science, 2006, v. 97, n. 7, p. 611, doi. 10.1111/j.1349-7006.2006.00227.x
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- Article
Distinct patterns of gene expression in hepatocellular carcinomas and adjacent non-cancerous, cirrhotic liver tissues in rats fed a choline-deficient, l-amino acid-defined diet.
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- Cancer Science, 2005, v. 96, n. 7, p. 414, doi. 10.1111/j.1349-7006.2005.00069.x
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- Article
GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly.
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- Asian Journal of Andrology, 2018, v. 20, n. 6, p. 629, doi. 10.4103/aja.aja_20_18
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- Article
Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations.
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- Genes & Nutrition, 2019, v. 14, n. 1, p. N.PAG, doi. 10.1186/s12263-019-0646-6
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- Article
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 6, p. 550, doi. 10.1002/mgg3.165
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- Article
Nonsense-associated altered splicing of MAP3K1 in two siblings with 46,XY disorders of sex development.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-74405-1
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- Article
Sex difference in the association of dietary fiber intake with visceral fat volume in Japanese adults.
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- European Journal of Nutrition, 2024, v. 63, n. 5, p. 1973, doi. 10.1007/s00394-024-03405-y
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- Article
Tamoxifen Treatment for Pubertal Gynecomastia in Two Siblings with Partial Androgen Insensitivity Syndrome.
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- Hormone Research in Paediatrics, 2014, v. 81, n. 3, p. 211, doi. 10.1159/000356923
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- Article
De novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency.
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- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 139, doi. 10.1159/000355380
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- Article
Carcinogenic risk of copper gluconate evaluated by a rat medium-term liver carcinogenicity bioassay protocol.
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- Archives of Toxicology, 2008, v. 82, n. 8, p. 563, doi. 10.1007/s00204-008-0294-x
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- Article
Rapid generation of mouse models with defined point mutations by the CRISPR/ Cas9 system.
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- Scientific Reports, 2014, p. 1, doi. 10.1038/srep05396
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- Article
Dihydrotestosterone induces minor transcriptional alterations in genital skin fibroblasts of children with and without androgen insensitivity.
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- Endocrine Journal, 2019, v. 66, n. 4, p. 387, doi. 10.1507/endocrj.ej18-0494
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- Article
Fertility preservation in a family with a novel NR5A1 mutation.
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- Endocrine Journal, 2015, v. 62, n. 3, p. 289, doi. 10.1507/endocrj.ej14-0340
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- Article
Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.
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- Endocrine Journal, 2013, v. 60, n. 8, p. 1013, doi. 10.1507/endocrj.ej13-0023
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- Article
Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.
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- Human Mutation, 2017, v. 38, n. 1, p. 39, doi. 10.1002/humu.23116
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- Article
Cover Image, Volume 38, Issue 1.
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- Human Mutation, 2017, v. 38, n. 1, p. i, doi. 10.1002/humu.23151
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- Article
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
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- PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206184
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- Article
Gain‐of‐function mutations in G‐protein–coupled receptor genes associated with human endocrine disorders.
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- Clinical Endocrinology, 2018, v. 88, n. 3, p. 351, doi. 10.1111/cen.13496
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- Article
Association between Dietary Behaviors and BMI Stratified by Sex and the ALDH2 rs671 Polymorphism in Japanese Adults.
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- Nutrients, 2022, v. 14, n. 23, p. 5116, doi. 10.3390/nu14235116
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- Article
A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations.
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- Nutrients, 2020, v. 12, n. 10, p. 3182, doi. 10.3390/nu12103182
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- Article