Pages that link to "Q15753061"
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The following pages link to Cancer Genetics and Cytogenetics (Q15753061):
Displaying 50 items.
- Loss of heterozygosity on 8p in prostate cancer implicates a role for dematin in tumor progression (Q22010806) (← links)
- Promoter hypermethylation of DLC-1, a candidate tumor suppressor gene, in several common human cancers (Q24170294) (← links)
- True extended haplotypes of p53: indicators of breast cancer risk (Q24170295) (← links)
- Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis (Q24294760) (← links)
- The transposase domain protein Metnase/SETMAR suppresses chromosomal translocations (Q24338398) (← links)
- NUT midline carcinoma (Q24629868) (← links)
- Coordinated expression of microRNA-155 and predicted target genes in diffuse large B-cell lymphoma (Q24648226) (← links)
- Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemia (Q24657303) (← links)
- hREC2, a RAD51-like gene, is disrupted by t(12;14) (q15;q24.1) in a uterine leiomyoma (Q28138064) (← links)
- Silent polymorphisms within the coding region of human sodium/hydrogen exchanger isoform-1 cDNA in peripheral blood mononuclear cells of leukemia patients: A comparison with healthy controls (Q28141960) (← links)
- hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas (Q28142829) (← links)
- Regional fine mapping of HMG17 to chromosomal band 1p35 (Q28142840) (← links)
- Unusual breakpoint distribution of 8p abnormalities in T-prolymphocytic leukemia: a study with YACS mapping to 8p11-p12 (Q28143068) (← links)
- Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability (Q28185113) (← links)
- Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types (Q28188279) (← links)
- Expression analysis of alpha-NAC and ANX2 in juvenile myelomonocytic leukemia using SMART polymerase chain reaction and "virtual Northern" hybridization (Q28191483) (← links)
- Chronic myelocytic leukemia with eosinophilia, t(9;12)(q34;p13), and ETV6-ABL gene rearrangement: case report and review of the literature (Q28198326) (← links)
- Expression of the HMGA2-LPP fusion transcript in only 1 of 61 karyotypically normal pulmonary chondroid hamartomas (Q28198360) (← links)
- Transcriptionally active chimeric gene derived from the fusion of the AML1 gene and a novel gene on chromosome 8 in t(8;21) leukemic cells (Q28201192) (← links)
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. gastrointestinal stromal tumors (Q28205404) (← links)
- Newly established clear cell sarcoma (malignant melanoma of soft parts) cell line expressing melanoma-associated Melan-A antigen and overexpressing C-MYC oncogene (Q28205414) (← links)
- THY1 expression is associated with tumor suppression of human ovarian cancer (Q28208018) (← links)
- PRAME gene expression in childhood acute lymphoblastic leukemia (Q28213901) (← links)
- Clinical implications of PRAME gene expression in childhood acute myeloid leukemia (Q28214116) (← links)
- Differential expression of TCL1 during pre-B-cell acute lymphoblastic leukemia progression (Q28215276) (← links)
- Alterations in the suppressor gene PPP2R1B in parathyroid hyperplasias and adenomas (Q28216902) (← links)
- Allelic loss at 10q26 in osteosarcoma in the region of the BUB3 and FGFR2 genes (Q28242226) (← links)
- ERG gene is translocated in an Ewing's sarcoma cell line (Q28247422) (← links)
- Identification of rare variants in the hLIMD1 gene in breast cancer (Q28250209) (← links)
- Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases (Q28259438) (← links)
- Overexpression of the novel oncogene SALL4 and activation of the Wnt/beta-catenin pathway in myelodysplastic syndromes (Q28259650) (← links)
- 6q deletion discriminates Waldenström macroglobulinemia from IgM monoclonal gammopathy of undetermined significance (Q28260593) (← links)
- Polysomy 13 in a canine prostate carcinoma underlining its significance in the development of prostate cancer (Q28260605) (← links)
- Specific clones of spontaneously evolving karyotypes generate individuality of cancers (Q28265382) (← links)
- Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma (Q28266696) (← links)
- Identification of inactivating mutations in the JAK1, SYNJ2, and CLPTM1 genes in prostate cancer cells using inhibition of nonsense-mediated decay and microarray analysis (Q28267477) (← links)
- Loss of let-7 binding sites resulting from truncations of the 3' untranslated region of HMGA2 mRNA in uterine leiomyomas (Q28270790) (← links)
- Loss of SDHB and NF1 genes in a malignant phyllodes tumor of the breast as detected by oligo-array comparative genomic hybridization (Q28270800) (← links)
- Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization (Q28272804) (← links)
- Amplification of MGC2177, PLAG1, PSMC6P, and LYN in a malignant mixed tumor of salivary gland detected by cDNA microarray with tyramide signal amplification (Q28272821) (← links)
- Paraganglioma in a 13-year-old girl: a novel SDHB gene mutation in the family? (Q28274653) (← links)
- Finer delineation and transcript map of the 7q31 locus deleted in myeloid neoplasms (Q28276175) (← links)
- Amplification and overexpression of genes in 17p11.2 ~ p12 in osteosarcoma (Q28278284) (← links)
- Expression patterns of the LPP-HMGA2 fusion transcript in pulmonary chondroid hamartomas with t(3;12)(q27 approximately 28;q14 approximately 15) (Q28280505) (← links)
- Physical mapping of the human chromosome 11q23 region containing the ataxia-telangiectasia locus (Q28283236) (← links)
- Association between gene expression profile and tumor invasion in oral squamous cell carcinoma (Q28283380) (← links)
- Expression of reciprocal fusion transcripts of the HMGIC and LPP genes in parosteal lipoma (Q28285389) (← links)
- Truncating mutations in the ACVR2 gene attenuates activin signaling in prostate cancer cells (Q28285748) (← links)
- Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12) (Q28291773) (← links)
- Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2 (Q28291888) (← links)