153 related articles for article (PubMed ID: 12576457)
21. Allele-specific loss of heterozygosity at the DAL-1/4.1B (EPB41L3) tumor-suppressor gene locus in the absence of mutation.
Kittiniyom K; Mastronardi M; Roemer M; Wells WA; Greenberg ER; Titus-Ernstoff L; Newsham IF
Genes Chromosomes Cancer; 2004 Jul; 40(3):190-203. PubMed ID: 15138999
[TBL] [Abstract][Full Text] [Related]
22. Loss of expression, and mutations of Smad 2 and Smad 4 in human cervical cancer.
Maliekal TT; Antony ML; Nair A; Paulmurugan R; Karunagaran D
Oncogene; 2003 Jul; 22(31):4889-97. PubMed ID: 12894231
[TBL] [Abstract][Full Text] [Related]
23. Gene dosage and mutational analyses of EGFR in oligodendrogliomas.
Franco-Hernandez C; Martinez-Glez V; Alonso ME; De Campos JM; Isla A; Vaquero J; Gutierrez M; Rey JA
Int J Oncol; 2007 Jan; 30(1):209-15. PubMed ID: 17143531
[TBL] [Abstract][Full Text] [Related]
24. Conservation and expression of an alternative 3' exon of Runx2 encoding a novel proline-rich C-terminal domain.
Terry A; Kilbey A; Vaillant F; Stewart M; Jenkins A; Cameron E; Neil JC
Gene; 2004 Jul; 336(1):115-25. PubMed ID: 15225881
[TBL] [Abstract][Full Text] [Related]
25. The folate receptor alpha is frequently overexpressed in osteosarcoma samples and plays a role in the uptake of the physiologic substrate 5-methyltetrahydrofolate.
Yang R; Kolb EA; Qin J; Chou A; Sowers R; Hoang B; Healey JH; Huvos AG; Meyers PA; Gorlick R
Clin Cancer Res; 2007 May; 13(9):2557-67. PubMed ID: 17473184
[TBL] [Abstract][Full Text] [Related]
26. Localization of a human reduced folate carrier protein in the mitochondrial as well as the cell membrane of leukemia cells.
Trippett TM; Garcia S; Manova K; Mody R; Cohen-Gould L; Flintoff W; Bertino JR
Cancer Res; 2001 Mar; 61(5):1941-7. PubMed ID: 11280750
[TBL] [Abstract][Full Text] [Related]
27. Resistance to multiple novel antifolates is mediated via defective drug transport resulting from clustered mutations in the reduced folate carrier gene in human leukaemia cell lines.
Rothem L; Ifergan I; Kaufman Y; Priest DG; Jansen G; Assaraf YG
Biochem J; 2002 Nov; 367(Pt 3):741-50. PubMed ID: 12139489
[TBL] [Abstract][Full Text] [Related]
28. Single nucleotide polymorphisms in the human reduced folate carrier: characterization of a high-frequency G/A variant at position 80 and transport properties of the His(27) and Arg(27) carriers.
Whetstine JR; Gifford AJ; Witt T; Liu XY; Flatley RM; Norris M; Haber M; Taub JW; Ravindranath Y; Matherly LH
Clin Cancer Res; 2001 Nov; 7(11):3416-22. PubMed ID: 11705857
[TBL] [Abstract][Full Text] [Related]
29. Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor beta gene.
Rivolta CM; Olcese MC; Belforte FS; Chiesa A; Gruñeiro-Papendieck L; Iorcansky S; Herzovich V; Cassorla F; Gauna A; Gonzalez-Sarmiento R; Targovnik HM
Mol Cell Probes; 2009; 23(3-4):148-53. PubMed ID: 19268523
[TBL] [Abstract][Full Text] [Related]
30. Factor XIII(A) subunit deficiency due to a homozygous 13-base pair deletion in exon 3 of the A subunit gene.
Aslam S; Bowen DJ; Mandalaki T; Gialeraki R; Standen GR
Am J Hematol; 1996 Oct; 53(2):77-80. PubMed ID: 8892731
[TBL] [Abstract][Full Text] [Related]
31. Pattern of mutations that results in loss of reduced folate carrier function under antifolate selective pressure augmented by chemical mutagenesis.
Zhao R; Sharina IG; Goldman ID
Mol Pharmacol; 1999 Jul; 56(1):68-76. PubMed ID: 10385685
[TBL] [Abstract][Full Text] [Related]
32. Status of the DPC4 tumor suppressor gene in sporadic colon adenocarcinoma of Croatian patients: identification of a novel somatic mutation.
Popović Hadzija M; Radosevic S; Kovacević D; Lukac J; Hadzija M; Spaventi R; Pavelić K; Kapitanović S
Mutat Res; 2004 Apr; 548(1-2):61-73. PubMed ID: 15063137
[TBL] [Abstract][Full Text] [Related]
33. COPS3 amplification and clinical outcome in osteosarcoma.
Yan T; Wunder JS; Gokgoz N; Gill M; Eskandarian S; Parkes RK; Bull SB; Bell RS; Andrulis IL
Cancer; 2007 May; 109(9):1870-6. PubMed ID: 17366602
[TBL] [Abstract][Full Text] [Related]
34. Genetic variants of chemokine receptor CCR7 in patients with systemic lupus erythematosus, Sjogren's syndrome and systemic sclerosis.
Kahlmann D; Davalos-Misslitz AC; Ohl L; Stanke F; Witte T; Förster R
BMC Genet; 2007 Jun; 8():33. PubMed ID: 17587445
[TBL] [Abstract][Full Text] [Related]
35. Mutational analysis of transforming growth factor-beta receptor type II and Smad3 tumor suppressor genes in prolactinomas.
Ikeda H
Brain Tumor Pathol; 2006 Apr; 23(1):7-12. PubMed ID: 18095113
[TBL] [Abstract][Full Text] [Related]
36. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
[TBL] [Abstract][Full Text] [Related]
37. Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.
Durocher F; Labrie Y; Soucy P; Sinilnikova O; Labuda D; Bessette P; Chiquette J; Laframboise R; Lépine J; Lespérance B; Ouellette G; Pichette R; Plante M; Tavtigian SV; Simard J
BMC Cancer; 2006 Sep; 6():230. PubMed ID: 17010193
[TBL] [Abstract][Full Text] [Related]
38. p21WAF1/CIP1 gene DNA sequencing and its expression in human osteosarcoma.
Liao WM; Zhang CL; Li FB; Zeng BF; Zeng YX
Chin Med J (Engl); 2004 Jun; 117(6):936-40. PubMed ID: 15198903
[TBL] [Abstract][Full Text] [Related]
39. Mutation analysis of exon 9 of the LDL receptor gene in Thai subjects with primary hypercholesterolemia.
Yamwong P; Pongrapeeporn KU; Thepsuriyanont P; Amornrattana A; Somkasettrin A; Sribhen K
J Med Assoc Thai; 2000 Nov; 83 Suppl 2():S81-8. PubMed ID: 11194027
[TBL] [Abstract][Full Text] [Related]
40. Eleven single nucleotide polymorphisms and one triple nucleotide insertion of the human TGF-beta III receptor gene.
Zippert R; Bässler A; Holmer SR; Hengstenberg C; Schunkert H
J Hum Genet; 2000; 45(4):250-3. PubMed ID: 10944857
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
