BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

281 related articles for article (PubMed ID: 38721146)

  • 1. Testicular differentiation in 46,XX DSD: an overview of genetic causes.
    Ferrari MTM; Silva ESDN; Nishi MY; Batista RL; Mendonca BB; Domenice S
    Front Endocrinol (Lausanne); 2024; 15():1385901. PubMed ID: 38721146
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disorders of Sex Development with Testicular Differentiation in SRY-Negative 46,XX Individuals: Clinical and Genetic Aspects.
    Grinspon RP; Rey RA
    Sex Dev; 2016; 10(1):1-11. PubMed ID: 27055195
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis and management of non-CAH 46,XX disorders/differences in sex development.
    Yavas Abalı Z; Guran T
    Front Endocrinol (Lausanne); 2024; 15():1354759. PubMed ID: 38812815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Duplication Upstream of SOX9 Associated with
    Mengen E; Kayhan G; Kocaay P; Uçaktürk SA
    J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):308-314. PubMed ID: 31476840
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review.
    Barros BA; Guaragna MS; Fabbri-Scallet H; Palandi de Mello M; Guerra-Júnior G; Maciel-Guerra AT
    Sex Dev; 2022; 16(4):242-251. PubMed ID: 36657429
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disorders of sexual development and associated changes in the pituitary-gonadal axis in dogs.
    Buijtels JJ; de Gier J; Kooistra HS; Grinwis GC; Naan EC; Zijlstra C; Okkens AC
    Theriogenology; 2012 Oct; 78(7):1618-26. PubMed ID: 22980090
    [TBL] [Abstract][Full Text] [Related]  

  • 7. NR5A1 gene variants repress the ovarian-specific WNT signaling pathway in 46,XX disorders of sex development patients.
    Knarston IM; Robevska G; van den Bergen JA; Eggers S; Croft B; Yates J; Hersmus R; Looijenga LHJ; Cameron FJ; Monhike K; Ayers KL; Sinclair AH
    Hum Mutat; 2019 Feb; 40(2):207-216. PubMed ID: 30350900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.
    Ürel Demir G; Doğan ÖA; Şimşek Kiper PÖ; Utine GE; Boduroğlu K; Gucer S; Alikaşifoğlu M
    Fetal Pediatr Pathol; 2017 Dec; 36(6):445-451. PubMed ID: 29220612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic control of typical and atypical sex development.
    Reyes AP; León NY; Frost ER; Harley VR
    Nat Rev Urol; 2023 Jul; 20(7):434-451. PubMed ID: 37020056
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A 46,XX Ovotesticular Disorder of Sex Development Likely Caused by a Steroidogenic Factor-1 (NR5A1) Variant.
    Swartz JM; Ciarlo R; Guo MH; Abrha A; Weaver B; Diamond DA; Chan YM; Hirschhorn JN
    Horm Res Paediatr; 2017; 87(3):191-195. PubMed ID: 27855412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.
    Seeherunvong T; Ukarapong S; McElreavey K; Berkovitz GD; Perera EM
    J Pediatr Endocrinol Metab; 2012; 25(1-2):121-3. PubMed ID: 22570960
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (
    Eozenou C; Gonen N; Touzon MS; Jorgensen A; Yatsenko SA; Fusee L; Kamel AK; Gellen B; Guercio G; Singh P; Witchel S; Berman AJ; Mainpal R; Totonchi M; Mohseni Meybodi A; Askari M; Merel-Chali T; Bignon-Topalovic J; Migale R; Costanzo M; Marino R; Ramirez P; Perez Garrido N; Berensztein E; Mekkawy MK; Schimenti JC; Bertalan R; Mazen I; McElreavey K; Belgorosky A; Lovell-Badge R; Rajkovic A; Bashamboo A
    Proc Natl Acad Sci U S A; 2020 Jun; 117(24):13680-13688. PubMed ID: 32493750
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Dujardin E; André M; Dewaele A; Mandon-Pépin B; Poulat F; Frambourg A; Thépot D; Jouneau L; Jolivet G; Pailhoux E; Pannetier M
    Elife; 2023 Oct; 12():. PubMed ID: 37847154
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.
    Igarashi M; Takasawa K; Hakoda A; Kanno J; Takada S; Miyado M; Baba T; Morohashi KI; Tajima T; Hata K; Nakabayashi K; Matsubara Y; Sekido R; Ogata T; Kashimada K; Fukami M
    Hum Mutat; 2017 Jan; 38(1):39-42. PubMed ID: 27610946
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.
    Lambert S; Peycelon M; Samara-Boustani D; Hyon C; Dumeige L; Peuchmaur M; Fiot E; Léger J; Simon D; Paye-Jaouen A; Bouligand J; Siffroi JP; Carel JC; McElreavey K; El Ghoneimi A; Brachet C; Bouvattier C; Martinerie L
    Clin Endocrinol (Oxf); 2021 Apr; 94(4):667-676. PubMed ID: 33296530
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Refining the regulatory region upstream of SOX9 associated with 46,XX testicular disorders of Sex Development (DSD).
    Hyon C; Chantot-Bastaraud S; Harbuz R; Bhouri R; Perrot N; Peycelon M; Sibony M; Rojo S; Piguel X; Bilan F; Gilbert-Dussardier B; Kitzis A; McElreavey K; Siffroi JP; Bashamboo A
    Am J Med Genet A; 2015 Aug; 167A(8):1851-8. PubMed ID: 25900885
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Methylation Patterns of SOX3, SOX9, and WNT4 Genes in Gonads of Dogs with XX (SRY-Negative) Disorder of Sexual Development.
    Salamon S; Flisikowski K; Switonski M
    Sex Dev; 2017; 11(2):86-93. PubMed ID: 28365713
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Predictive value of anatomical findings and karyotype analysis in the diagnosis of patients with disorders of sexual development.
    Arcari AJ; Bergadá I; Rey RA; Gottlieb S
    Sex Dev; 2007; 1(4):222-9. PubMed ID: 18391533
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant.
    Gomes NL; de Paula LCP; Silva JM; Silva TE; Lerário AM; Nishi MY; Batista RL; Faria Júnior JAD; Moraes D; Costa EMF; Hemesath TP; Guaragna-Filho G; Leite JCL; Carvalho CG; Domenice S; Costa EC; Mendonca BB
    Clin Genet; 2019 Jan; 95(1):172-176. PubMed ID: 30294972
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.