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Increase in GFAP-positive astrocytes in histone demethylase GASC1/ KDM4C/ JMJD2C hypomorphic mutant mice.
- Published in:
- Genes to Cells, 2016, v. 21, n. 3, p. 218, doi. 10.1111/gtc.12331
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- Article
Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent.
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- Journal of Human Genetics, 2015, v. 60, n. 4, p. 203, doi. 10.1038/jhg.2014.123
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- Article
Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line.
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- Oncogene, 2000, v. 19, n. 37, p. 4302, doi. 10.1038/sj.onc.1203786
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- Article
Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15.
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- Oncogene, 2000, v. 19, n. 33, p. 3739, doi. 10.1038/sj.onc.1203716
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- Article
ANA, a novel member of Tob/BTG1 family, is expressed in the ventricular zone of the developing central nervous system.
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- Oncogene, 1998, v. 16, n. 20, p. 2687, doi. 10.1038/sj.onc.1201805
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- Article
Identification of an Efs isoform that lacks the SH3 domain and chromosomal mapping of human Efs.
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- Oncogene, 1997, v. 15, n. 14, p. 1741, doi. 10.1038/sj.onc.1201346
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- Article
Chromosomal aberrations in colorectal cancers and liver metastases analyzed by comparative genomic hybridization.
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- International Journal of Cancer, 2001, v. 94, n. 5, p. 623, doi. 10.1002/ijc.1522
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- Article
Amplification and over-expression of the AIB1 nuclear receptor co-activator gene in primary gastric cancers.
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- International Journal of Cancer, 2000, v. 89, n. 3, p. 217, doi. 10.1002/1097-0215(20000520)89:3<217::AID-IJC2>3.0.CO;2-6
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- Article
The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separase.
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- Journal of Cell Biology, 2006, v. 172, n. 6, p. 835, doi. 10.1083/jcb.200511126
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- Article
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 191, doi. 10.1038/jhg.2011.154
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- Article
Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.
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- Journal of Human Genetics, 2012, v. 57, n. 1, p. 73, doi. 10.1038/jhg.2011.131
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- Article
HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome.
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- Journal of Human Genetics, 2011, v. 56, n. 10, p. 707, doi. 10.1038/jhg.2011.85
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- Article
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 590, doi. 10.1038/jhg.2010.74
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- Article
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.
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- Journal of Human Genetics, 2010, v. 55, n. 4, p. 244, doi. 10.1038/jhg.2010.14
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- Article
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia.
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- Journal of Human Genetics, 2009, v. 54, n. 6, p. 355, doi. 10.1038/jhg.2009.40
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- Article
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 643, doi. 10.1007/s10038-007-0154-1
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- Article
Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.
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- Journal of Human Genetics, 2007, v. 52, n. 5, p. 397, doi. 10.1007/s10038-007-0127-4
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- Article
Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion ofSNF5/INI1in a newly established cell line derived from extrarenal rhabdoid tumor.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 586, doi. 10.1007/s10038-004-0191-y
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- Article
Association of over-expressed TFDP1 with progression of hepatocellular carcinomas.
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- Journal of Human Genetics, 2003, v. 48, n. 12, p. 609, doi. 10.1007/s10038-003-0086-3
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- Article
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines.
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- Journal of Human Genetics, 2003, v. 48, n. 6, p. 331, doi. 10.1007/s10038-003-0026-2
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- Article
Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 1, doi. 10.1007/s100380050096
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- Article
Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterations.
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- Carcinogenesis, 2011, v. 32, n. 4, p. 462, doi. 10.1093/carcin/bgq274
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- Article
YAP is a candidate oncogene for esophageal squamous cell carcinoma.
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- Carcinogenesis, 2011, v. 32, n. 3, p. 389, doi. 10.1093/carcin/bgq254
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- Article
Frequent silencing of protocadherin 17, a candidate tumour suppressor for esophageal squamous cell carcinoma.
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- Carcinogenesis, 2010, v. 31, n. 6, p. 1027, doi. 10.1093/carcin/bgq053
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- Article
miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma.
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- Carcinogenesis, 2010, v. 31, n. 5, p. 766, doi. 10.1093/carcin/bgp250
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- Article
Resequencing and copy number analysis of the human tyrosine kinase gene family in poorly differentiated gastric cancer.
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- Carcinogenesis, 2009, v. 30, n. 11, p. 1857, doi. 10.1093/carcin/bgp206
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- Article
Overexpression of SMYD2 relates to tumor cell proliferation and malignant outcome of esophageal squamous cell carcinoma.
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- Carcinogenesis, 2009, v. 30, n. 7, p. 1139, doi. 10.1093/carcin/bgp116
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- Article
Genome-wide DNA methylation profiles in both precancerous conditions and clear cell renal cell carcinomas are correlated with malignant potential and patient outcome.
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- Carcinogenesis, 2009, v. 30, n. 2, p. 214, doi. 10.1093/carcin/bgn268
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- Article
Novel targets for the 18p11.3 amplification frequently observed in esophageal squamous cell carcinomas.
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- Carcinogenesis, 2002, v. 23, n. 1, p. 19, doi. 10.1093/carcin/23.1.19
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- Article
Frequent silencing of DBC1 is by genetic or epigenetic mechanisms in non-small cell lung cancers.
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- Human Molecular Genetics, 2005, v. 14, n. 8, p. 997, doi. 10.1093/hmg/ddi092
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- Article
Missing Y Chromosome in Ph1-Negative Chronic Myeloid Leukemia with bcr Rearrangement.
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- Acta Haematologica, 1991, v. 85, n. 1, p. 51, doi. 10.1159/000204855
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- Article
Long Arm Deletion of Chromosome 7 Unrelated to Original Karyotype in Recurrent t(8;21) Acute Myeloblastic Leukemia.
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- Acta Haematologica, 1990, v. 83, n. 3, p. 159, doi. 10.1159/000205196
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- Article
Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31-33 in Cell Lines from Nonpapillary Carcinomas.
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- Cancer Science, 2000, v. 91, n. 2, p. 156, doi. 10.1111/j.1349-7006.2000.tb00927.x
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- Article
Multiple Primary Cancers with Microsatellite Instability: Report of a Case.
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- Cancer Science, 1996, v. 87, n. 1, p. 105, doi. 10.1111/j.1349-7006.1996.tb00207.x
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- Article
Chromosomal Assignment of the Gene for Protein Tyrosine Phosphatase HPTPδ.
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- Cancer Science, 1993, v. 84, n. 12, p. 1219, doi. 10.1111/j.1349-7006.1993.tb02825.x
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- Article
Physical Ordering of Three Polymorphic DNA Markers Spanning the Regions Containing a Tumor Suppressor Gene of Renal Cell Carcinoma by Three-color Fluorescent in situ Hybridization.
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- Cancer Science, 1992, v. 83, n. 12, p. 1248, doi. 10.1111/j.1349-7006.1992.tb02753.x
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- Article
p53 gene mutation is not directly related to tumoricidal effects of preoperative radiochemohyperthermia therapy for rectal cancers.
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- Journal of Surgical Oncology, 1996, v. 63, n. 2, p. 87, doi. 10.1002/(SICI)1096-9098(199610)63:2<87::AID-JSO3>3.0.CO;2-K
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- Article
Identification of target genes within an amplicon at 14q12-q13 in esophageal squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 32, n. 2, p. 112, doi. 10.1002/gcc.1172
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- Article
Homozygous deletion in a neuroblastoma cell line defined by a high-density STS map spanning human chromosome band 1p36.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 4, p. 326, doi. 10.1002/gcc.1151
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- Article
CD44 is a potential target of amplification within the 11p13 amplicon detected in gastric cancer cell lines.
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- Genes, Chromosomes & Cancer, 2000, v. 29, n. 4, p. 315, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1047>3.0.CO;2-E
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- Article
Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 336, doi. 10.1002/(SICI)1098-2264(199912)26:4<336::AID-GCC8>3.0.CO;2-H
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- Article
Comparative genomic hybridization of squamous cell carcinoma of the esophagus: The possible involvement of the DP1 gene in the 13q34 amplicon.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 4, p. 337, doi. 10.1002/(SICI)1098-2264(199904)24:4<337::AID-GCC7>3.0.CO;2-O
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- Article
Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 4, p. 299, doi. 10.1002/(SICI)1098-2264(199904)24:4<299::AID-GCC2>3.0.CO;2-U
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- Article
Amplification on double-minute chromosomes and partial-tandem duplication of the MILL gene in leukemic cells of a patient with acute myelogenous leukemia.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 3, p. 267, doi. 10.1002/(SICI)1098-2264(199811)23:3<267::AID-GCC10>3.0.CO;2-J
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- Article
Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double-target fluorescence in situ hybridization and microsatellite analysis.
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- Genes, Chromosomes & Cancer, 1995, v. 14, n. 4, p. 295, doi. 10.1002/gcc.2870140408
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- Article
Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses.
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- Genes, Chromosomes & Cancer, 1994, v. 9, n. 1, p. 57, doi. 10.1002/gcc.2870090110
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- Article
Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2.
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- Genes, Chromosomes & Cancer, 1993, v. 6, n. 4, p. 235, doi. 10.1002/gcc.2870060408
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- Article
Familial nasal NK/T-cell lymphoma and pesticide use.
- Published in:
- American Journal of Hematology, 2001, v. 66, n. 2, p. 145, doi. 10.1002/1096-8652(200102)66:2<145::AID-AJH1033>3.0.CO;2-V
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- Article
Myelomonocytic crisis with t(5;17) and a p53 mutation in a patient with chronic myelogenous leukemia.
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- American Journal of Hematology, 1994, v. 45, n. 4, p. 335, doi. 10.1002/ajh.2830450412
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- Article
Distribution of breakpoint within the breakpoint cluster region ( bcr) in chronic myelogenous leukemia with a complex philadelphia chromosome translocation.
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- American Journal of Hematology, 1989, v. 32, n. 3, p. 194, doi. 10.1002/ajh.2830320307
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- Article