BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 36780715)

  • 1. Bioinformatics analysis and verification of hub genes in 46,XY, disorders of sexual development.
    Cao Z; Liu L; Bu Z; Yang Z; Li Y; Li R
    Reprod Fertil Dev; 2023 Mar; 35(5):353-362. PubMed ID: 36780715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular genetics of disorders of sex development in a highly consanguineous population.
    Alswailem M; Alsagheir A; Abbas BB; Alzahrani O; Alzahrani AS
    J Steroid Biochem Mol Biol; 2021 Apr; 208():105736. PubMed ID: 32784047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of Hub Genes in Hemifacial Microsomia: Evidence From Bioinformatic Analysis.
    Zhao S; Sun P; Li X; Xu X; Peng Q; Shu K; Ma L; Liang Y; Liu B; Zhang Z
    J Craniofac Surg; 2022 Mar-Apr 01; 33(2):e145-e149. PubMed ID: 34855631
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Bioinformatics Analysis Identifies Hub Genes and Molecular Pathways Involved in Sepsis-Induced Myopathy.
    Ning YL; Yang ZQ; Xian SX; Lin JZ; Lin XF; Chen WT
    Med Sci Monit; 2020 Feb; 26():e919665. PubMed ID: 32008037
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development.
    Li L; Zhang J; Li Q; Qiao L; Li P; Cui Y; Li S; Hao S; Wu T; Liu L; Yin J; Hu P; Dou X; Li S; Yang H
    Ital J Pediatr; 2022 Mar; 48(1):47. PubMed ID: 35331321
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Preliminary investigation of gender assignment in 46,XY disorders of sex development with severe male undermasculinisation].
    Wu DH; Tian HJ; Yuan JN; Dong GP; Wu DW; Yang RW; Sun LY; Tang DX; Fu JF
    Zhonghua Er Ke Za Zhi; 2019 Oct; 57(10):786-791. PubMed ID: 31594066
    [No Abstract]   [Full Text] [Related]  

  • 15. SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation.
    Fernández-Cancio M; Audí L; Andaluz P; Torán N; Piró C; Albisu M; Gussinyé M; Yeste D; Clemente M; Martínez-Mora J; Blanco A; Granada ML; Marco M; Ferragut J; López-Siguero JP; Beneyto M; Carles C; Carrascosa A
    Int J Androl; 2011 Dec; 34(6 Pt 2):e526-35. PubMed ID: 21631525
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.
    Dong Y; Yi Y; Yao H; Yang Z; Hu H; Liu J; Gao C; Zhang M; Zhou L; Asan ; Yi X; Liang Z
    BMC Med Genet; 2016 Mar; 17():23. PubMed ID: 26980296
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development.
    Xu Y; Wang Y; Li N; Yao R; Li G; Li J; Ding Y; Chen Y; Huang X; Chen Y; Qing Y; Yu T; Shen Y; Wang X; Shen Y; Wang J
    Eur J Endocrinol; 2019 Sep; 181(3):311-323. PubMed ID: 31277073
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel Deleterious Mutation in Steroid-5α-Reductase-2 in 46, XY Disorders of Sex Development: Case Report Study.
    Rafigh M; Salmaninejad A; Sorouri Khorashad B; Arabi A; Milanizadeh S; Hiradfar M; Abbaszadegan MR
    Fetal Pediatr Pathol; 2022 Feb; 41(1):141-148. PubMed ID: 32449406
    [No Abstract]   [Full Text] [Related]  

  • 19. Etiological diagnosis of undervirilized male/XY disorder of sex development.
    Atta I; Ibrahim M; Parkash A; Lone SW; Khan YN; Raza J
    J Coll Physicians Surg Pak; 2014 Oct; 24(10):714-8. PubMed ID: 25327912
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of 46, XY Disorder of Sex Development (DSD) Based on Plasma Cell-Free DNA and Targeted Next-Generation Sequencing.
    De Falco L; Piscopo C; D'Angelo R; Evangelista E; Suero T; Sirica R; Ruggiero R; Savarese G; Di Carlo A; Furino G; Scarpato C; Fico A
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946839
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.