BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 31687637)

  • 1. The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing
    Carvalheira G; Malinverni AM; Moysés-Oliveira M; Ueta R; Cardili L; Monteagudo P; Mathez ALG; Verreschi IT; Maluf MA; Shida MEF; Leite MTC; Mazzotti D; Melaragno MI; Dias-da-Silva MR
    J Endocr Soc; 2019 Nov; 3(11):2107-2113. PubMed ID: 31687637
    [TBL] [Abstract][Full Text] [Related]  

  • 2. COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitors.
    Ferreira LGA; Kizys MML; Gama GAC; Pachernegg S; Robevska G; Sinclair AH; Ayers KL; Dias-da-Silva MR
    Cell Biosci; 2024 Jan; 14(1):3. PubMed ID: 38178246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children.
    Bashamboo A; Eozenou C; Jorgensen A; Bignon-Topalovic J; Siffroi JP; Hyon C; Tar A; Nagy P; Sólyom J; Halász Z; Paye-Jaouen A; Lambert S; Rodriguez-Buritica D; Bertalan R; Martinerie L; Rajpert-De Meyts E; Achermann JC; McElreavey K
    Am J Hum Genet; 2018 Mar; 102(3):487-493. PubMed ID: 29478779
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development.
    Hattori A; Fukami M
    Biomolecules; 2023 Apr; 13(4):. PubMed ID: 37189438
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CORRIGENDUM FOR "The Natural History of a Man With Ovotesticular 46,XX DSD Due to a Novel 3-Mb 15q26.2 Deletion Containing
    J Endocr Soc; 2020 Mar; 4(3):bvaa022. PubMed ID: 32175518
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development.
    Ledig S; Hiort O; Wünsch L; Wieacker P
    Eur J Endocrinol; 2012 Jul; 167(1):119-24. PubMed ID: 22573722
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region.
    Dangle P; Touzon MS; Reyes-Múgica M; Witchel SF; Rajkovic A; Schneck FX; Yatsenko SA
    J Med Genet; 2017 Oct; 54(10):705-709. PubMed ID: 28483799
    [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. Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development.
    Şimşek E; Binay Ç; Demiral M; Tokar B; Kabukçuoğlu S; Üstün M
    J Clin Res Pediatr Endocrinol; 2016 Sep; 8(3):351-5. PubMed ID: 27087521
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Association between polymorphisms in the SOX9 region and canine disorder of sex development (78,XX; SRY-negative) revisited in a multibreed case-control study.
    Nowacka-Woszuk J; Szczerbal I; Stachowiak M; Szydlowski M; Nizanski W; Dzimira S; Maslak A; Payan-Carreira R; Wydooghe E; Nowak T; Switonski M
    PLoS One; 2019; 14(6):e0218565. PubMed ID: 31220175
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.
    Domenice S; Machado AZ; Ferreira FM; Ferraz-de-Souza B; Lerario AM; Lin L; Nishi MY; Gomes NL; da Silva TE; Silva RB; Correa RV; Montenegro LR; Narciso A; Costa EM; Achermann JC; Mendonca BB
    Birth Defects Res C Embryo Today; 2016 Dec; 108(4):309-320. PubMed ID: 28033660
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs.
    Nowacka-Woszuk J; Stachowiak M; Szczerbal I; Szydlowski M; Szabelska-Beresewicz A; Zyprych-Walczak J; Krzeminska P; Nowak T; Lukomska A; Ligocka Z; Biezynski J; Dzimira S; Nizanski W; Switonski M
    Genomics; 2022 Jul; 114(4):110389. PubMed ID: 35597501
    [TBL] [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. A Rare Case of Testicular Disorder of Sex Development in a Dog (78,XX; SRY-Negative) with Male External Genitalia and Detection of Copy Number Variation in the Region Upstream of the SOX9 Gene.
    Szczerbal I; Nowacka-Woszuk J; Dzimira S; Atamaniuk W; Nizanski W; Switonski M
    Sex Dev; 2016; 10(2):74-8. PubMed ID: 27089505
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.