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Retention of Chromosome 3 in Extrapulmonary Small Cell Cancer Shown by Molecular and Cytogenetic Studies.
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- JNCI: Journal of the National Cancer Institute, 1989, v. 81, n. 16, p. 1223, doi. 10.1093/jnci/81.16.1223
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- Publication type:
- Article
Specific Genetic Change in Tumors Associated With von Hippel-Lindau Disease.
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- JNCI: Journal of the National Cancer Institute, 1989, v. 81, n. 14, p. 1097
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- Publication type:
- Article
Genetic Changes in Human Adrenocortical Carcinomas.
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- JNCI: Journal of the National Cancer Institute, 1989, v. 81, n. 7, p. 518
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- Publication type:
- Article
Improved Detection of Allele Loss in Renal Cell Carcinomas After Removal of Leukocytes by Immunologic Selection.
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- JNCI: Journal of the National Cancer Institute, 1989, v. 81, n. 4, p. 287, doi. 10.1093/jnci/81.4.287
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- Publication type:
- Article
The genetic basis of cancer of kidney cancer: implications for gene-specific clinical management.
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- BJU International, 2005, v. 95, p. 2, doi. 10.1111/j.1464-410X.2005.05189.x
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- Article
Subcellular localization of the von Hippel-Lindau disease gene product is cell cycle-dependent.
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- International Journal of Cancer, 1998, v. 78, n. 1, p. 62, doi. 10.1002/(SICI)1097-0215(19980925)78:1<62::AID-IJC11>3.0.CO;2-7
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- Publication type:
- Article
Serotherapy of cancer: Cellular changes in primary rat mammary carcinomas after infusion of syngeneic sera absorbed with protein a-sepharose.
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- International Journal of Cancer, 1988, v. 42, n. 1, p. 76, doi. 10.1002/ijc.2910420115
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- Publication type:
- Article
Expression of Birt-Hogg-Dubé gene mRNA in normal and neoplastic human tissues.
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- Modern Pathology, 2004, v. 17, n. 8, p. 998, doi. 10.1038/modpathol.3800152
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- Publication type:
- Article
Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: Modeling studies.
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- Proteins, 2001, v. 44, n. 1, p. 32, doi. 10.1002/prot.1069
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- Publication type:
- Article
Immunotherapy of guinea pig cancer with bcg.
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- Cancer (0008543X), 1974, v. 34, n. S8, p. 1532, doi. 10.1002/1097-0142(197410)34:8+<1532::AID-CNCR2820340827>3.0.CO;2-H
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- Publication type:
- Article
Familial Pheochromocytoma Associated with a Novel Mutation in the von Hippel-Lindau Gene.
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- Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 1, p. 147, doi. 10.1210/jc.81.1.147
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- Publication type:
- Article
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: A strategy for cloning the putative tumor suppressor gene.
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- Genes, Chromosomes & Cancer, 1992, v. 5, n. 2, p. 119, doi. 10.1002/gcc.2870050205
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- Publication type:
- Article
Involvement of the RAFI locus, at band 3p25, in the 3p deletion of small-cell lung cancer.
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- Genes, Chromosomes & Cancer, 1991, v. 3, n. 4, p. 283, doi. 10.1002/gcc.2870030407
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- Article
Molecular mapping of deletion sites in the short arm of chromosome 3 in human lung cancer.
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- Genes, Chromosomes & Cancer, 1990, v. 1, n. 3, p. 240, doi. 10.1002/gcc.2870010309
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- Publication type:
- Article
Kidney-Targeted Birt-Hogg-Dubé Gene Inactivation in a Mouse Model: Erkl/2 and Akt-mTOR Activation, Cell Hyperproliferation, and Polycystic Kidneys.
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- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 2, p. 140, doi. 10.1093/jnci/djm288
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- Publication type:
- Article
High Frequency of Somatic Frameshift BHD Gene Mutations in Birt-Hogg-Dubé-Associated Renal Tumors.
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- JNCI: Journal of the National Cancer Institute, 2005, v. 97, n. 12, p. 931, doi. 10.1093/jnci/dji154
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- Publication type:
- Article
Clinical research priorities in renal cell carcinoma: renal cell carcinoma chemoprevention strategies including target populations, proposed agents, and clinical trial designs--Workgroup No. 6. Union Internationale Contre le Cancer (UICC) and the American Joint Committee on Cancer (AJCC).
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- 1997
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- Publication type:
- journal article
SEROLOGIC SURVEYS OF HUMAN CANCER PATIENTS FOR ANTIBODY TO ADENOVIRUS T ANTIGENS.
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- American Journal of Epidemiology, 1970, v. 91, n. 5, p. 500
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- Article
INDUCTION OF TUMOR IMMUNITY BY INTRATUMORAL CHEMOTHERAPY.
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- Annals of the New York Academy of Sciences, 1976, v. 276, n. 1, p. 565, doi. 10.1111/j.1749-6632.1976.tb41683.x
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- Article
A novel germ line juxtamembrane Met mutation in human gastric cancer.
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- Oncogene, 2000, v. 19, n. 43, p. 4947, doi. 10.1038/sj.onc.1203874
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- Publication type:
- Article
Tumorigenesis mediated by MET mutant M1268T is inhibited by dominant-negative Src.
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- Oncogene, 2000, v. 19, n. 26, p. 2996, doi. 10.1038/sj.onc.1203628
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- Publication type:
- Article
Novel mutations of the MET proto-oncogene in papillary renal carcinomas.
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- Oncogene, 1999, v. 18, n. 14, p. 2343, doi. 10.1038/sj.onc.1202547
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- Publication type:
- Article
Gene structure of the human MET proto-oncogene.
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- Oncogene, 1997, v. 15, n. 13, p. 1583, doi. 10.1038/sj.onc.1201338
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- Publication type:
- Article
Von Hippel-Lindau Syndrome.
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- Brain Pathology, 1995, v. 5, n. 2, p. 181, doi. 10.1111/j.1750-3639.1995.tb00592.x
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- Publication type:
- Article
Lung Cysts, Spontaneous Pneumothorax, and Genetic Associations in 89 Families with Birt-Hogg-Dubé Syndrome.
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- American Journal of Respiratory & Critical Care Medicine, 2007, v. 175, n. 10, p. 1044, doi. 10.1164/rccm.200610-1483OC
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- Publication type:
- Article
Polymerase chain reaction-single-strand conformation polymorphism analysis for the VHL gene in chemically induced kidney tumors of rats using intron-derived primers.
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- Molecular Carcinogenesis, 1997, v. 19, n. 4, p. 230, doi. 10.1002/(SICI)1098-2744(199708)19:4<230::AID-MC3>3.0.CO;2-G
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- Publication type:
- Article
H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation.
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- Human Molecular Genetics, 2017, v. 26, n. 2, p. 354, doi. 10.1093/hmg/ddw392
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- Publication type:
- Article
Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von hippel-lindau disease-associated, and familial pheochromocytoma.
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- Genes, Chromosomes & Cancer, 1995, v. 13, n. 3, p. 151, doi. 10.1002/gcc.2870130303
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- Publication type:
- Article
Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors.
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- Genes, Chromosomes & Cancer, 1994, v. 11, n. 1, p. 15, doi. 10.1002/gcc.2870110104
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- Publication type:
- Article
Inhibition of murine sarcoma virus oncogenesis with living BCG.
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- International Journal of Cancer, 1971, v. 8, n. 2, p. 320, doi. 10.1002/ijc.2910080218
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- Publication type:
- Article
Cover, Volume 42, Issue 5.
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- Human Mutation, 2021, v. 42, n. 5, p. i, doi. 10.1002/humu.24209
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- Publication type:
- Article
Comprehensive characterization of Alu‐mediated breakpoints in germline VHL gene deletions and rearrangements in patients from 71 VHL families.
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- Human Mutation, 2021, v. 42, n. 5, p. 520, doi. 10.1002/humu.24194
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- Publication type:
- Article
Somatic Alterations Contributing to Metastasis of a Castration-Resistant Prostate Cancer.
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- Human Mutation, 2013, v. 34, n. 9, p. 1231, doi. 10.1002/humu.22346
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- Article
A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog.
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- Human Molecular Genetics, 2003, v. 12, n. 23, p. 3043, doi. 10.1093/hmg/ddg336
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- Publication type:
- Article
Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 641, doi. 10.1093/hmg/11.6.641
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- Publication type:
- Article
Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas.
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- Nature Genetics, 1998, v. 20, n. 1, p. 66, doi. 10.1038/1727
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- Article
Solid renal tumor severity in von Hippel Lindau disease is related to germline deletion length and location (Communicated by Gregg L. Semenza).
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- Human Mutation, 2004, v. 23, n. 1, p. 40, doi. 10.1002/humu.10302
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- Publication type:
- Article
Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods.
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- Human Mutation, 2001, v. 17, n. 3, p. 210, doi. 10.1002/humu.6
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- Publication type:
- Article
Signature-based analysis of MET proto-oncogene mutations using DHPLC.
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- Human Mutation, 2000, v. 16, n. 1, p. 68, doi. 10.1002/1098-1004(200007)16:1<68::AID-HUMU12>3.0.CO;2-U
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- Publication type:
- Article
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
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- Human Mutation, 1998, v. 12, n. 6, p. 417, doi. 10.1002/(SICI)1098-1004(1998)12:6<417::AID-HUMU8>3.0.CO;2-K
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- Publication type:
- Article
Germline mutations in the Von Hippel-Lindau disease ( VHL) gene in families from North America, Europe, and Japan.
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- Human Mutation, 1996, v. 8, n. 4, p. 348, doi. 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3
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- Publication type:
- Article
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.
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- Human Molecular Genetics, 1995, v. 4, n. 11, p. 2139
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- Article
Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotype.
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- Human Molecular Genetics, 1994, v. 3, n. 8, p. 1303
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- Article
A novel donor splice site mutation associated with two mRNAs in von Hippel — Lindau disease.
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- Human Molecular Genetics, 1994, v. 3, n. 7, p. 1191
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- Publication type:
- Article
Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene.
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- Human Molecular Genetics, 1994, v. 3, n. 4, p. 595
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- Publication type:
- Article
Three tetranucleotide polymorphisms for loci: D3S1352; D3S1358; D3S1359.
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- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1327
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- Publication type:
- Article
Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435.
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- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1326
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- Publication type:
- Article
Mapping the Von Hippel — Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis.
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- Human Molecular Genetics, 1993, v. 2, n. 7, p. 879
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- Publication type:
- Article
Three tetrameric repeat polymorphisms on human chromosome 3: D3S1349; D3S1350; D3S1351.
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- Human Molecular Genetics, 1993, v. 2, n. 6, p. 819
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- Publication type:
- Article
Six dinucleotide microsatellite polymorphisms on human chromosome 3.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 6, p. 817
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- Publication type:
- Article