90 related articles for article (PubMed ID: 26011025)
1. Congenital mirror movements caused by a mutation in the DCC gene.
Meneret A; Trouillard O; Brochard V; Roze E
Dev Med Child Neurol; 2015 Aug; 57(8):776. PubMed ID: 26011025
[No Abstract] [Full Text] [Related]
2. A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
Depienne C; Cincotta M; Billot S; Bouteiller D; Groppa S; Brochard V; Flamand C; Hubsch C; Meunier S; Giovannelli F; Klebe S; Corvol JC; Vidailhet M; Brice A; Roze E
Neurology; 2011 Jan; 76(3):260-4. PubMed ID: 21242494
[TBL] [Abstract][Full Text] [Related]
3. Mutations in DCC cause congenital mirror movements.
Srour M; Rivière JB; Pham JM; Dubé MP; Girard S; Morin S; Dion PA; Asselin G; Rochefort D; Hince P; Diab S; Sharafaddinzadeh N; Chouinard S; Théoret H; Charron F; Rouleau GA
Science; 2010 Apr; 328(5978):592. PubMed ID: 20431009
[TBL] [Abstract][Full Text] [Related]
4. A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
Djarmati-Westenberger A; Brüggemann N; Espay AJ; Bhatia KP; Klein C
Neurology; 2011 Oct; 77(16):1580. PubMed ID: 22006891
[No Abstract] [Full Text] [Related]
5. Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.
Collins Hutchinson ML; St-Onge J; Schlienger S; Boudrahem-Addour N; Mougharbel L; Michaud JF; Lloyd C; Bruneau E; Roux C; Sahly AN; Osterman B; Myers KA; Rouleau GA; Jimenez Cruz DA; Rivière JB; Accogli A; Charron F; Srour M
Mov Disord; 2024 Feb; 39(2):400-410. PubMed ID: 38314870
[TBL] [Abstract][Full Text] [Related]
6. "On the other hand": a case of hereditary, congenital mirror movement.
Chan YC; Ho KH
Singapore Med J; 2002 Jun; 43(6):312-3. PubMed ID: 12380730
[TBL] [Abstract][Full Text] [Related]
7. Mirror Hand Movements Caused by a Deletion of the DCC Gene.
Kleinendorst L; van Haelst MM
JAMA Neurol; 2024 Feb; 81(2):187. PubMed ID: 38048091
[TBL] [Abstract][Full Text] [Related]
8. Clinical significance of p53, K-ras and DCC gene alterations in the stage I-II colorectal cancers.
Akkiprik M; Ataizi-Celikel C; Düşünceli F; Sönmez O; Gulluoglu BM; Sav A; Ozer A
J Gastrointestin Liver Dis; 2007 Mar; 16(1):11-7. PubMed ID: 17410283
[TBL] [Abstract][Full Text] [Related]
9. RAD51 deficiency disrupts the corticospinal lateralization of motor control.
Gallea C; Popa T; Hubsch C; Valabregue R; Brochard V; Kundu P; Schmitt B; Bardinet E; Bertasi E; Flamand-Roze C; Alexandre N; Delmaire C; Méneret A; Depienne C; Poupon C; Hertz-Pannier L; Cincotta M; Vidailhet M; Lehericy S; Meunier S; Roze E
Brain; 2013 Nov; 136(Pt 11):3333-46. PubMed ID: 24056534
[TBL] [Abstract][Full Text] [Related]
10. Loss of DCC gene expression is of prognostic importance in acute myelogenous leukemia.
Inokuchi K; Yamaguchi H; Hanawa H; Tanosaki S; Nakamura K; Tarusawa M; Miyake K; Shimada T; Dan K
Clin Cancer Res; 2002 Jun; 8(6):1882-8. PubMed ID: 12060632
[TBL] [Abstract][Full Text] [Related]
11. Expression and mutational analysis of the DCC, DPC4, and MADR2/JV18-1 genes in neuroblastoma.
Kong XT; Choi SH; Inoue A; Xu F; Chen T; Takita J; Yokota J; Bessho F; Yanagisawa M; Hanada R; Yamamoto K; Hayashi Y
Cancer Res; 1997 Sep; 57(17):3772-8. PubMed ID: 9288786
[TBL] [Abstract][Full Text] [Related]
12. "Dancing feet dyskinesias": a clue to parkin gene mutations.
Chang FC; Mehta P; Koentjoro B; Latt M; Blair N; Nicholson G; Sue CM; Fung VS
Mov Disord; 2012 Apr; 27(4):587-8. PubMed ID: 22287053
[No Abstract] [Full Text] [Related]
13. The DCC gene and colorectal cancer: the story is more complex.
Beggs AD; Abulafi M; Hodgson SV
Colorectal Dis; 2008 Jul; 10(6):630. PubMed ID: 18266884
[No Abstract] [Full Text] [Related]
14. Analysis of the DCC tumor suppressor gene in testicular germ cell tumors: mutations and loss of expression.
Strohmeyer D; Langenhof S; Ackermann R; Hartmann M; Strohmeyer T; Schmidt B
J Urol; 1997 May; 157(5):1973-6. PubMed ID: 9112574
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of genetic mutations of tumor suppresser genes in colorectal cancer patients.
Kubo H; Miki C; Kusunoki M
Hepatogastroenterology; 2004; 51(55):114-7. PubMed ID: 15011843
[TBL] [Abstract][Full Text] [Related]
16. Suppressed tumorigenicity of human endometrial cancer cells by the restored expression of the DCC gene.
Kato H; Zhou Y; Asanoma K; Kondo H; Yoshikawa Y; Watanabe K; Matsuda T; Wake N; Barrett JC
Br J Cancer; 2000 Jan; 82(2):459-66. PubMed ID: 10646905
[TBL] [Abstract][Full Text] [Related]
17. DCC expression and prognosis in colorectal cancer.
Banerjee AK
Lancet; 1997 Apr; 349(9057):968. PubMed ID: 9100619
[No Abstract] [Full Text] [Related]
18. Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.
Franz EA; Chiaroni-Clarke R; Woodrow S; Glendining KA; Jasoni CL; Robertson SP; Gardner RJM; Markie D
J Neurol Sci; 2015 Apr; 351(1-2):140-145. PubMed ID: 25813273
[TBL] [Abstract][Full Text] [Related]
19. Point mutations and allelic deletion of tumor suppressor gene DCC in human esophageal squamous cell carcinomas and their relation to metastasis.
Miyake S; Nagai K; Yoshino K; Oto M; Endo M; Yuasa Y
Cancer Res; 1994 Jun; 54(11):3007-10. PubMed ID: 8187090
[TBL] [Abstract][Full Text] [Related]
20. Congenital mirror movements in a child with Chiari type 1 malformation.
Krishnakumar P; Jisha P
Indian Pediatr; 2007 Feb; 44(2):152-3. PubMed ID: 17351312
[No Abstract] [Full Text] [Related]
[Next] [New Search]