95 related articles for article (PubMed ID: 26582524)
1. [Progress in the molecular genetic mechanism of gonadoblastoma].
Yu LL; Dong WR; Chen MH; Kong XY
Yi Chuan; 2015 Nov; 37(11):1105-15. PubMed ID: 26582524
[TBL] [Abstract][Full Text] [Related]
2. A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.
Hersmus R; van der Zwan YG; Stoop H; Bernard P; Sreenivasan R; Oosterhuis JW; Brüggenwirth HT; de Boer S; White S; Wolffenbuttel KP; Alders M; McElreavy K; Drop SL; Harley VR; Looijenga LH
PLoS One; 2012; 7(7):e40858. PubMed ID: 22815844
[TBL] [Abstract][Full Text] [Related]
3. A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma.
Hersmus R; de Leeuw BH; Stoop H; Bernard P; van Doorn HC; Brüggenwirth HT; Drop SL; Oosterhuis JW; Harley VR; Looijenga LH
Eur J Hum Genet; 2009 Dec; 17(12):1642-9. PubMed ID: 19513096
[TBL] [Abstract][Full Text] [Related]
4. Yolk sac tumor and dysgerminoma in the left gonad following gonadoblastoma in the right gonad in a 46,XY DSD with a novel SRY missense mutation: a case report.
Xie C; Cai J; Li N; Hua P; Yang Z; Yu X; Tang D; Hu Y; Liu Q
BMC Pregnancy Childbirth; 2023 Jan; 23(1):58. PubMed ID: 36694125
[TBL] [Abstract][Full Text] [Related]
5. Identification of germ cells at risk for neoplastic transformation in gonadoblastoma: an immunohistochemical study for OCT3/4 and TSPY.
Kersemaekers AM; Honecker F; Stoop H; Cools M; Molier M; Wolffenbuttel K; Bokemeyer C; Li Y; Lau YF; Oosterhuis JW; Looijenga LH
Hum Pathol; 2005 May; 36(5):512-21. PubMed ID: 15948118
[TBL] [Abstract][Full Text] [Related]
6. FOXL2 and SOX9 distinguish the lineage of the sex cord-stromal cells in gonadoblastomas.
Buell-Gutbrod R; Ivanovic M; Montag A; Lengyel E; Fadare O; Gwin K
Pediatr Dev Pathol; 2011; 14(5):391-5. PubMed ID: 21682576
[TBL] [Abstract][Full Text] [Related]
7. Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome.
Subbiah V; Huff V; Wolff JE; Ketonen L; Lang FF; Stewart J; Langford L; Herzog CE
Pediatr Blood Cancer; 2009 Dec; 53(7):1349-51. PubMed ID: 19653292
[TBL] [Abstract][Full Text] [Related]
8. Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
Bastian C; Muller JB; Lortat-Jacob S; Nihoul-Fékété C; Bignon-Topalovic J; McElreavey K; Bashamboo A; Brauner R
Fertil Steril; 2015 May; 103(5):1297-304. PubMed ID: 25813279
[TBL] [Abstract][Full Text] [Related]
9. A Novel SRY Gene Mutation p.F109L in a 46,XY Female with Complete Gonadal Dysgenesis.
Andonova S; Robeva R; Sirakov M; Mainhard K; Tomova A; Ledig S; Kumanov P; Savov A
Sex Dev; 2015; 9(6):333-7. PubMed ID: 26871559
[TBL] [Abstract][Full Text] [Related]
10. Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development.
Benko S; Gordon CT; Mallet D; Sreenivasan R; Thauvin-Robinet C; Brendehaug A; Thomas S; Bruland O; David M; Nicolino M; Labalme A; Sanlaville D; Callier P; Malan V; Huet F; Molven A; Dijoud F; Munnich A; Faivre L; Amiel J; Harley V; Houge G; Morel Y; Lyonnet S
J Med Genet; 2011 Dec; 48(12):825-30. PubMed ID: 22051515
[TBL] [Abstract][Full Text] [Related]
11. Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma.
Lau Y; Chou P; Iezzoni J; Alonzo J; Kömüves L
Cytogenet Cell Genet; 2000; 91(1-4):160-4. PubMed ID: 11173850
[TBL] [Abstract][Full Text] [Related]
12. Gene symbol: SRY.
Heine-Suñer D; Torres-Juan L; Gómez C; Pérez-Granero A; Bernues M; Govea N; Roseli J
Hum Genet; 2007 Feb; 120(6):909. PubMed ID: 17438599
[No Abstract] [Full Text] [Related]
13. Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome.
Schumacher V; Gueler B; Looijenga LH; Becker JU; Amann K; Engers R; Dotsch J; Stoop H; Schulz W; Royer-Pokora B
Mol Reprod Dev; 2008 Sep; 75(9):1484-94. PubMed ID: 18271004
[TBL] [Abstract][Full Text] [Related]
14. Utility of OCT3/4, TSPY and β-catenin as biological markers for gonadoblastoma formation and malignant germ cell tumor development in dysgenetic gonads.
Palma I; Garibay N; Pena-Yolanda R; Contreras A; Raya A; Dominguez C; Romero M; Aristi G; Queipo G
Dis Markers; 2013; 34(6):419-24. PubMed ID: 23396295
[TBL] [Abstract][Full Text] [Related]
15. 46 XY pure gonadal dysgenesis with gonadoblastoma and dysgerminoma.
Ben Temime R; Chachial A; Attial L; Ghodbanel I; Makhloufl T; Koubaal A; Kourda N; Ben Jilani S; Dammak T; El May A; Rahal K
Tunis Med; 2008 Jul; 86(7):710-3. PubMed ID: 19472738
[TBL] [Abstract][Full Text] [Related]
16. Gonadoblastoma and hepatoid and endometrioid-like yolk sac tumor: an update.
Ulbright TM
Int J Gynecol Pathol; 2014 Jul; 33(4):365-73. PubMed ID: 24901396
[TBL] [Abstract][Full Text] [Related]
17. "Dissecting Gonadoblastoma" of Scully: A Morphologic Variant That Often Mimics Germinoma.
Kao CS; Idrees MT; Young RH; Ulbright TM
Am J Surg Pathol; 2016 Oct; 40(10):1417-23. PubMed ID: 27454939
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation (c. 341A>G) in the SRY gene in a 46,XY female patient with gonadal dysgenesis.
Helszer Z; Dmochowska A; Szemraj J; Słowikowska-Hilczer J; Wieczorek M; Jędrzejczyk S; Kałużewski B
Gene; 2013 Sep; 526(2):467-70. PubMed ID: 23624391
[TBL] [Abstract][Full Text] [Related]
19. WT1 Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the Literature.
Mazen I; Hassan H; Kamel A; Mekkawy M; McElreavey K; Essawi M
Sex Dev; 2017; 11(5-6):280-283. PubMed ID: 29320783
[TBL] [Abstract][Full Text] [Related]
20. WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report.
Finken MJ; Hendriks YM; van der Voorn JP; Veening MA; Lombardi MP; Rotteveel J
Horm Res Paediatr; 2015; 83(3):211-6. PubMed ID: 25613702
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
