207 related articles for article (PubMed ID: 27267075)
1. Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer.
Disciglio V; Devecchi A; Palumbo O; Carella M; Penso D; Milione M; Valle G; Pierotti MA; Vitellaro M; Bertario L; Canevari S; Signoroni S; De Cecco L
Chin J Cancer; 2016 Jun; 35(1):51. PubMed ID: 27267075
[TBL] [Abstract][Full Text] [Related]
2. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
[TBL] [Abstract][Full Text] [Related]
3. Novel pathogenic variants in the androgen receptor gene associated with androgen insensitivity syndrome identified through exome sequencing and in silico analysis.
Li C; Wang X; Wang X; Li X; Chen W; Zhao M; Liu X; Li P; Xue M
Gene; 2023 Apr; 860():147225. PubMed ID: 36708848
[TBL] [Abstract][Full Text] [Related]
4. Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.
Bellido F; Sowada N; Mur P; Lázaro C; Pons T; Valdés-Mas R; Pineda M; Aiza G; Iglesias S; Soto JL; Urioste M; Caldés T; Balbín M; Blay P; Rueda D; Durán M; Valencia A; Moreno V; Brunet J; Blanco I; Navarro M; Calin GA; Borck G; Puente XS; Capellá G; Valle L
Gastroenterology; 2018 Jan; 154(1):181-194.e20. PubMed ID: 28912018
[TBL] [Abstract][Full Text] [Related]
5. The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome.
Ilaslan E; Markosyan R; Sproll P; Stevenson BJ; Sajek M; Sajek MP; Hayrapetyan H; Sarkisian T; Livshits L; Nef S; Jaruzelska J; Kusz-Zamelczyk K
Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33182400
[TBL] [Abstract][Full Text] [Related]
6. Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.
Köhler B; Lumbroso S; Leger J; Audran F; Grau ES; Kurtz F; Pinto G; Salerno M; Semitcheva T; Czernichow P; Sultan C
J Clin Endocrinol Metab; 2005 Jan; 90(1):106-11. PubMed ID: 15522944
[TBL] [Abstract][Full Text] [Related]
7. Systematic search for rare variants in Finnish early-onset colorectal cancer patients.
Tanskanen T; Gylfe AE; Katainen R; Taipale M; Renkonen-Sinisalo L; Järvinen H; Mecklin JP; Böhm J; Kilpivaara O; Pitkänen E; Palin K; Vahteristo P; Tuupanen S; Aaltonen LA
Cancer Genet; 2015; 208(1-2):35-40. PubMed ID: 25749350
[TBL] [Abstract][Full Text] [Related]
8. Novel compound variants of the AR and MAP3K1 genes are related to the clinical heterogeneity of androgen insensitivity syndrome.
Cheng Y; Sun Y; Ji Y; Jiang D; Teng G; Zhou X; Zhou X; Li G; Xu C
Biosci Rep; 2020 May; 40(5):. PubMed ID: 32338288
[TBL] [Abstract][Full Text] [Related]
9. Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.
Radpour R; Falah M; Aslani A; Zhong XY; Saleki A
J Androl; 2009; 30(3):230-2. PubMed ID: 19023143
[TBL] [Abstract][Full Text] [Related]
10. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
11. Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer.
de Voer RM; Hahn MM; Mensenkamp AR; Hoischen A; Gilissen C; Henkes A; Spruijt L; van Zelst-Stams WA; Kets CM; Verwiel ET; Nagtegaal ID; Schackert HK; van Kessel AG; Hoogerbrugge N; Ligtenberg MJ; Kuiper RP
Sci Rep; 2015 Sep; 5():14060. PubMed ID: 26358404
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome.
Ahmed SF; Cheng A; Dovey L; Hawkins JR; Martin H; Rowland J; Shimura N; Tait AD; Hughes IA
J Clin Endocrinol Metab; 2000 Feb; 85(2):658-65. PubMed ID: 10690872
[TBL] [Abstract][Full Text] [Related]
13. A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair.
Boardman LA; Schmidt S; Lindor NM; Burgart LJ; Cunningham JM; Price-Troska T; Snow K; Ahlquist DA; Thibodeau SN
Genes Chromosomes Cancer; 2001 Feb; 30(2):181-6. PubMed ID: 11135435
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.
Boehmer AL; Brinkmann AO; Nijman RM; Verleun-Mooijman MC; de Ruiter P; Niermeijer MF; Drop SL
J Clin Endocrinol Metab; 2001 Mar; 86(3):1240-6. PubMed ID: 11238515
[TBL] [Abstract][Full Text] [Related]
15. Androgen insensitivity syndrome in a cohort of Sri Lankan children with 46, XY disorders of sex development (46, XY DSD).
de Silva KS; Sirisena ND; Wijenayaka HK; Cooray JG; Jayasekara RW; Dissanayake VH
Ceylon Med J; 2015 Dec; 60(4):139-42. PubMed ID: 26778393
[TBL] [Abstract][Full Text] [Related]
16. Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
Yurgelun MB; Masciari S; Joshi VA; Mercado RC; Lindor NM; Gallinger S; Hopper JL; Jenkins MA; Buchanan DD; Newcomb PA; Potter JD; Haile RW; Kucherlapati R; Syngal S;
JAMA Oncol; 2015 May; 1(2):214-21. PubMed ID: 26086041
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.
Mazen I; Soliman H; El-Gammal M; Torky A; Mekkawy M; Abdel-Hamid MS; Essawi M
Horm Res Paediatr; 2014; 82(6):411-4. PubMed ID: 25034089
[TBL] [Abstract][Full Text] [Related]
18. Novel and recurrent mutations in patients with androgen insensitivity syndromes.
Ledig S; Jakubiczka S; Neulen J; Aulepp U; Burck-Lehmann U; Mohnike K; Thiele H; Zierler H; Brewer C; Wieacker P
Horm Res; 2005; 63(6):263-9. PubMed ID: 15925895
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred.
Zhu YS; Cai LQ; Cordero JJ; Canovatchel WJ; Katz MD; Imperato-McGinley J
J Clin Endocrinol Metab; 1999 May; 84(5):1590-4. PubMed ID: 10323385
[TBL] [Abstract][Full Text] [Related]
20. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development.
Topcu V; Ilgin-Ruhi H; Siklar Z; Karabulut HG; Berberoglu M; Hacihamdioglu B; Savas-Erdeve S; Aycan Z; Peltek-Kendirci HN; Ocal G; Tukun FA
J Pediatr Endocrinol Metab; 2015 Nov; 28(11-12):1257-63. PubMed ID: 26197461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
