196 related articles for article (PubMed ID: 10749657)
1. Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.
Hagan DM; Ross AJ; Strachan T; Lynch SA; Ruiz-Perez V; Wang YM; Scambler P; Custard E; Reardon W; Hassan S; Nixon P; Papapetrou C; Winter RM; Edwards Y; Morrison K; Barrow M; Cordier-Alex MP; Correia P; Galvin-Parton PA; Gaskill S; Gaskin KJ; Garcia-Minaur S; Gereige R; Hayward R; Homfray T
Am J Hum Genet; 2000 May; 66(5):1504-15. PubMed ID: 10749657
[TBL] [Abstract][Full Text] [Related]
2. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
Köchling J; Karbasiyan M; Reis A
Eur J Hum Genet; 2001 Aug; 9(8):599-605. PubMed ID: 11528505
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
Crétolle C; Pelet A; Sanlaville D; Zérah M; Amiel J; Jaubert F; Révillon Y; Baala L; Munnich A; Nihoul-Fékété C; Lyonnet S
Hum Mutat; 2008 Jul; 29(7):903-10. PubMed ID: 18449898
[TBL] [Abstract][Full Text] [Related]
4. Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
Garcia-Barceló M; So MT; Lau DK; Leon TY; Yuan ZW; Cai WS; Lui VC; Fu M; Herbrick JA; Gutter E; Proud V; Li L; Pierre-Louis J; Aleck K; van Heurn E; Belloni E; Scherer SW; Tam PK
Clin Chem; 2006 Jan; 52(1):46-52. PubMed ID: 16254195
[TBL] [Abstract][Full Text] [Related]
5. Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.
Kim IS; Oh SY; Choi SJ; Kim JH; Park KH; Park HK; Kim JW; Ki CS
J Hum Genet; 2007; 52(8):698-701. PubMed ID: 17612791
[TBL] [Abstract][Full Text] [Related]
6. A previously unreported mutation in a Currarino syndrome kindred.
Wang RY; Jones JR; Chen S; Rogers RC; Friez MJ; Schwartz CE; Graham JM
Am J Med Genet A; 2006 Sep; 140(18):1923-30. PubMed ID: 16906559
[TBL] [Abstract][Full Text] [Related]
7. MNX1 (HLXB9) mutations in Currarino patients.
Garcia-Barceló MM; Lui VC; So MT; Miao X; Leon TY; Yuan ZW; Ngan ES; Ehsan T; Chung PH; Khong PL; Wong KK; Tam PK
J Pediatr Surg; 2009 Oct; 44(10):1892-8. PubMed ID: 19853743
[TBL] [Abstract][Full Text] [Related]
8. [Currarino syndrome: variability of imaging findings in 22 molecular-genetically identified (HLXB9 mutation) patients from five families].
Riebel T; Köchling J; Scheer I; Oellinger J; Reis A
Rofo; 2004 Apr; 176(4):564-9. PubMed ID: 15088182
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome.
Zu S; Winberg J; Arnberg F; Palmer G; Svensson PJ; Wester T; Nordenskjöld A
J Pediatr Surg; 2011 Jul; 46(7):1390-5. PubMed ID: 21763840
[TBL] [Abstract][Full Text] [Related]
10. Clinical features and HLXB9 gene mutation of a sporadic Chinese Currarino's syndrome case.
Liang Y; Wang J; Cai W
J Pediatr Surg; 2007 Jun; 42(6):E27-30. PubMed ID: 17560192
[TBL] [Abstract][Full Text] [Related]
11. HLXB9 homeobox gene and caudal regression syndrome.
Merello E; De Marco P; Mascelli S; Raso A; Calevo MG; Torre M; Cama A; Lerone M; Martucciello G; Capra V
Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):205-9. PubMed ID: 16498628
[TBL] [Abstract][Full Text] [Related]
12. Involvement of the HLXB9 homeobox gene in Currarino syndrome.
Belloni E; Martucciello G; Verderio D; Ponti E; Seri M; Jasonni V; Torre M; Ferrari M; Tsui LC; Scherer SW
Am J Hum Genet; 2000 Jan; 66(1):312-9. PubMed ID: 10631160
[No Abstract] [Full Text] [Related]
13. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
14. Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome.
Verlinsky Y; Rechitsky S; Schoolcraft W; Kuliev A
Am J Med Genet A; 2005 Apr; 134A(1):103-4. PubMed ID: 15776399
[No Abstract] [Full Text] [Related]
15. Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome.
Lee S; Kim EJ; Cho SI; Park H; Seo SH; Seong MW; Park SS; Jung SE; Lee SC; Park KW; Kim HY
Ann Lab Med; 2018 May; 38(3):242-248. PubMed ID: 29401559
[TBL] [Abstract][Full Text] [Related]
16. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
Ross AJ; Ruiz-Perez V; Wang Y; Hagan DM; Scherer S; Lynch SA; Lindsay S; Custard E; Belloni E; Wilson DI; Wadey R; Goodman F; Orstavik KH; Monclair T; Robson S; Reardon W; Burn J; Scambler P; Strachan T
Nat Genet; 1998 Dec; 20(4):358-61. PubMed ID: 9843207
[TBL] [Abstract][Full Text] [Related]
17. Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype.
Markljung E; Adamovic T; Cao J; Naji H; Kaiser S; Wester T; Nordenskjöld A
Gene; 2012 Oct; 507(1):50-3. PubMed ID: 22820079
[TBL] [Abstract][Full Text] [Related]
18. Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia.
Volk A; Karbasiyan M; Semmler A; Todt U; Urbach H; Klockgether T; Linnebank M
Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):249-51. PubMed ID: 17183586
[TBL] [Abstract][Full Text] [Related]
19. The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndrome.
Romano F; De Marco P; Ognibene M; Di Duca M; Baldassari S; Pavanello M; Piatelli G; Zara F; Capra V
Birth Defects Res; 2021 Sep; 113(15):1161-1165. PubMed ID: 34156759
[TBL] [Abstract][Full Text] [Related]
20. HLXB9 gene expression, and nuclear location during in vitro neuronal differentiation in the SK-N-BE neuroblastoma cell line.
Leotta CG; Federico C; Brundo MV; Tosi S; Saccone S
PLoS One; 2014; 9(8):e105481. PubMed ID: 25136833
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
