164 related articles for article (PubMed ID: 18985462)
1. Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.
Shoichet SA; Waibel S; Endruhn S; Sperfeld AD; Vorwerk B; Müller I; Erdogan F; Ludolph AC; Ropers HH; Ullmann R
Amyotroph Lateral Scler; 2009 Jun; 10(3):162-9. PubMed ID: 18985462
[TBL] [Abstract][Full Text] [Related]
2. Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.
Takahashi Y; Seki N; Ishiura H; Mitsui J; Matsukawa T; Kishino A; Onodera O; Aoki M; Shimozawa N; Murayama S; Itoyama Y; Suzuki Y; Sobue G; Nishizawa M; Goto J; Tsuji S
Arch Neurol; 2008 Oct; 65(10):1326-32. PubMed ID: 18852346
[TBL] [Abstract][Full Text] [Related]
3. Pathways and genes differentially expressed in the motor cortex of patients with sporadic amyotrophic lateral sclerosis.
Lederer CW; Torrisi A; Pantelidou M; Santama N; Cavallaro S
BMC Genomics; 2007 Jan; 8():26. PubMed ID: 17244347
[TBL] [Abstract][Full Text] [Related]
4. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
Erdogan F; Larsen LA; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen JR; Schubert M; Jurkatis J; Tzschach A; Ropers HH; Ullmann R
J Med Genet; 2008 Nov; 45(11):704-9. PubMed ID: 18713793
[TBL] [Abstract][Full Text] [Related]
5. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
[TBL] [Abstract][Full Text] [Related]
6. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
[TBL] [Abstract][Full Text] [Related]
7. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
Blauw HM; Veldink JH; van Es MA; van Vught PW; Saris CG; van der Zwaag B; Franke L; Burbach JP; Wokke JH; Ophoff RA; van den Berg LH
Lancet Neurol; 2008 Apr; 7(4):319-26. PubMed ID: 18313986
[TBL] [Abstract][Full Text] [Related]
8. Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.
Saillour Y; Cossée M; Leturcq F; Vasson A; Beugnet C; Poirier K; Commere V; Sublemontier S; Viel M; Letourneur F; Barbot JC; Deburgrave N; Chelly J; Bienvenu T
Hum Mutat; 2008 Sep; 29(9):1083-90. PubMed ID: 18683213
[TBL] [Abstract][Full Text] [Related]
9. Gene expressions specifically detected in motor neurons (dynactin 1, early growth response 3, acetyl-CoA transporter, death receptor 5, and cyclin C) differentially correlate to pathologic markers in sporadic amyotrophic lateral sclerosis.
Jiang YM; Yamamoto M; Tanaka F; Ishigaki S; Katsuno M; Adachi H; Niwa J; Doyu M; Yoshida M; Hashizume Y; Sobue G
J Neuropathol Exp Neurol; 2007 Jul; 66(7):617-27. PubMed ID: 17620987
[TBL] [Abstract][Full Text] [Related]
10. [Molecular pathogenesis of motor neuron disease].
Sobue G
Rinsho Shinkeigaku; 2001 Dec; 41(12):1070-1. PubMed ID: 12235798
[TBL] [Abstract][Full Text] [Related]
11. Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia.
Moon HJ; Yim SV; Lee WK; Jeon YW; Kim YH; Ko YJ; Lee KS; Lee KH; Han SI; Rha HK
Biochem Biophys Res Commun; 2006 Jun; 344(2):531-9. PubMed ID: 16630559
[TBL] [Abstract][Full Text] [Related]
12. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.
Edelmann L; Hirschhorn K
Ann N Y Acad Sci; 2009 Jan; 1151():157-66. PubMed ID: 19154522
[TBL] [Abstract][Full Text] [Related]
13. Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.
Cronin S; Blauw HM; Veldink JH; van Es MA; Ophoff RA; Bradley DG; van den Berg LH; Hardiman O
Hum Mol Genet; 2008 Nov; 17(21):3392-8. PubMed ID: 18689356
[TBL] [Abstract][Full Text] [Related]
14. Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
Froyen G; Van Esch H; Bauters M; Hollanders K; Frints SG; Vermeesch JR; Devriendt K; Fryns JP; Marynen P
Hum Mutat; 2007 Oct; 28(10):1034-42. PubMed ID: 17546640
[TBL] [Abstract][Full Text] [Related]
15. Experimental analysis of oligonucleotide microarray design criteria to detect deletions by comparative genomic hybridization.
Flibotte S; Moerman DG
BMC Genomics; 2008 Oct; 9():497. PubMed ID: 18940006
[TBL] [Abstract][Full Text] [Related]
16. Identification of DNA copy number aberrations associated with metastases of colorectal cancer using array CGH profiles.
Nakao M; Kawauchi S; Furuya T; Uchiyama T; Adachi J; Okada T; Ikemoto K; Oga A; Sasaki K
Cancer Genet Cytogenet; 2009 Jan; 188(2):70-6. PubMed ID: 19100508
[TBL] [Abstract][Full Text] [Related]
17. Utility of array comparative genomic hybridization in cytogenetic analysis.
Singh RR; Cheung KJ; Horsman DE
Methods Mol Biol; 2011; 730():219-34. PubMed ID: 21431645
[TBL] [Abstract][Full Text] [Related]
18. Microarray-based comparative genomic hybridization (array-CGH) as a useful tool for identifying genes involved in Glioblastoma (GB).
Ruano Y; Mollejo M; de Lope AR; Hernández-Moneo JL; Martínez P; Meléndez B
Methods Mol Biol; 2010; 653():35-45. PubMed ID: 20721736
[TBL] [Abstract][Full Text] [Related]
19. Comparative genome hybridization array analysis for sporadic Parkinson's disease.
Kim JS; Yoo JY; Lee KS; Kim HS; Choi JS; Rha HK; Yim SV; Lee KH
Int J Neurosci; 2008 Sep; 118(9):1331-45. PubMed ID: 18698514
[TBL] [Abstract][Full Text] [Related]
20. Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genes.
Schraders M; Jares P; Bea S; Schoenmakers EF; van Krieken JH; Campo E; Groenen PJ
Br J Haematol; 2008 Oct; 143(2):210-21. PubMed ID: 18699851
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
