These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 37147882)

  • 1. The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development.
    Zhang W; Mao J; Wang X; Zhao Z; Zhang X; Sun B; Cao Y; Nie M; Wu X
    Andrology; 2024 Jan; 12(1):98-108. PubMed ID: 37147882
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype and genetic characteristics in 20 Chinese patients with 46,XY disorders of sex development.
    Zheng GY; Chu GM; Li PP; He R
    J Endocrinol Invest; 2023 Aug; 46(8):1613-1622. PubMed ID: 36745277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application and insights of targeted next-generation sequencing in a large cohort of 46,XY disorders of sex development in Chinese.
    Chen H; Chen G; Li F; Huang Y; Zhu L; Zhao Y; Jiang Z; Yan X; Yu L
    Biol Sex Differ; 2024 Sep; 15(1):73. PubMed ID: 39285472
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development.
    Mazen I; Mekkawy M; Kamel A; Essawi M; Hassan H; Abdel-Hamid M; Amr K; Soliman H; El-Ruby M; Torky A; El Gammal M; Elaidy A; Bashamboo A; McElreavey K
    Am J Med Genet A; 2021 Jun; 185(6):1666-1677. PubMed ID: 33742552
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of gene mutations in a Chinese 46,XY disorders of sex development cohort detected by targeted next-generation sequencing.
    Yu BQ; Liu ZX; Gao YJ; Wang X; Mao JF; Nie M; Wu XY
    Asian J Androl; 2021; 23(1):69-73. PubMed ID: 32985417
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
    Kulkarni V; Chellasamy SK; Dhangar S; Ghatanatti J; Vundinti BR
    Mol Hum Reprod; 2023 Jan; 29(2):. PubMed ID: 36617173
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel NR5A1 mutations found in Chinese patients with 46, XY disorders of sex development.
    Yu B; Liu Z; Gao Y; Mao J; Wang X; Hao M; Ma W; Huang Q; Zhang R; Nie M; Wu X
    Clin Endocrinol (Oxf); 2018 Nov; 89(5):613-620. PubMed ID: 30103258
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development.
    Rjiba K; Mougou-Zerelli S; Hamida IH; Saad G; Khadija B; Jelloul A; Slimani W; Hasni Y; Dimassi S; Khelifa HB; Sallem A; Kammoun M; Abdallah HH; Gribaa M; Bignon-Topalovic J; Chelly S; Khairi H; Bibi M; Kacem M; Saad A; Bashamboo A; McElreavey K
    Reprod Biol Endocrinol; 2023 Jan; 21(1):2. PubMed ID: 36631813
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Targeted Next-Generation Sequencing for the Diagnosis of Gene Variants in Patients with 46,XY Disorder of Sex Development.
    Guo Q; Zhong WW; Lai HJ; Ye L; Zhang YF; Li JT; Qiu JG; Wang J
    Sex Dev; 2023; 17(1):26-31. PubMed ID: 36689917
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypes.
    Wang H; Zhang L; Wang N; Zhu H; Han B; Sun F; Yao H; Zhang Q; Zhu W; Cheng T; Cheng K; Liu Y; Zhao S; Song H; Qiao J
    Hum Genet; 2018 Mar; 137(3):265-277. PubMed ID: 29582157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and functional analysis of fourteen NR5A1 variants in patients with the 46 XY disorders of sex development.
    Na X; Mao Y; Tang Y; Jiang W; Yu J; Cao L; Yang J
    Gene; 2020 Nov; 760():145004. PubMed ID: 32738419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening of MAMLD1 mutations in 70 children with 46,XY DSD: identification and functional analysis of two new mutations.
    Kalfa N; Fukami M; Philibert P; Audran F; Pienkowski C; Weill J; Pinto G; Manouvrier S; Polak M; Ogata T; Sultan C
    PLoS One; 2012; 7(3):e32505. PubMed ID: 22479329
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin?
    Camats N; Fernández-Cancio M; Audí L; Schaller A; Flück CE
    Eur J Hum Genet; 2018 Sep; 26(9):1329-1338. PubMed ID: 29891883
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The importance of the multiplex ligation-dependent probe amplification in the identification of a novel two-exon deletion of the NR5A1 gene in a patient with 46,XY differences of sex development.
    Nagy O; Kárteszi J; Hartwig M; Bertalan R; Jávorszky E; Erhardt É; Patócs A; Tornóczky T; Balogh I; Ujfalusi A
    Mol Biol Rep; 2019 Oct; 46(5):5595-5601. PubMed ID: 31338750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 46,XY disorders of sex development: the use of NGS for prevalent variants.
    Xie QG; Luo P; Xia K; Li ZQ; Xu Z; Su C; Deng CH
    Hum Genet; 2022 Dec; 141(12):1863-1873. PubMed ID: 35729303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparison between two inhibin B ELISA assays in 46,XY testicular disorders of sex development (DSD) with normal testosterone secretion.
    Guaragna-Filho G; Calixto AR; De Paula GB; De Oliveira LC; Morcillo AM; De Mello MP; Maciel-Guerra AT; Guerra-Junior G
    J Pediatr Endocrinol Metab; 2018 Jan; 31(2):191-194. PubMed ID: 29306929
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variants of
    Martínez de LaPiscina I; Mahmoud RA; Sauter KS; Esteva I; Alonso M; Costa I; Rial-Rodriguez JM; Rodríguez-Estévez A; Vela A; Castano L; Flück CE
    Int J Mol Sci; 2020 Nov; 21(22):. PubMed ID: 33202802
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic Findings.
    Globa E; Zelinska N; Shcherbak Y; Bignon-Topalovic J; Bashamboo A; MсElreavey K
    Front Endocrinol (Lausanne); 2022; 13():810782. PubMed ID: 35432193
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?
    Fabbri-Scallet H; Werner R; Guaragna MS; de Andrade JGR; Maciel-Guerra AT; Hornig NC; Hiort O; Guerra-Júnior G; de Mello MP
    Sex Dev; 2022; 16(4):252-260. PubMed ID: 35764069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular investigation of mutations in androgen receptor and 5-alpha-reductase-2 genes in 46,XY Disorders of Sex Development with normal testicular development.
    Ahmadifard M; Kajbafzadeh A; Panjeh-Shahi S; Vand-Rajabpour F; Ahmadi-Beni R; Arshadi H; Setoodeh A; Rostami P; Tavakkoly-Bazzaz J; Tabrizi M
    Andrologia; 2019 Jun; 51(5):e13250. PubMed ID: 30815925
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.