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Reply to Fusaro.
- Published in:
- International Journal of Cancer, 2000, v. 87, n. 5, p. 756, doi. 10.1002/1097-0215(20000901)87:5<756::AID-IJC21>3.0.CO;2-N
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- Article
Characterization of ligurian melanoma families and risk of occurrence of other neoplasia.
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- International Journal of Cancer, 1999, v. 83, n. 4, p. 441, doi. 10.1002/(SICI)1097-0215(19991112)83:4<441::AID-IJC2>3.0.CO;2-R
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- Article
Functional analysis of a CDKN2A 5’UTR germline variant associated with pancreatic cancer development.
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- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189123
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- Article
MC1R variation and melanoma risk in relation to host/clinical and environmental factors in CDKN2A positive and negative melanoma patients.
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- Experimental Dermatology, 2012, v. 21, n. 9, p. 718, doi. 10.1111/j.1600-0625.2012.01549.x
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- Article
Functional analysis of CDKN2A/p16INK4a 5′-UTR variants predisposing to melanoma.
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- Human Molecular Genetics, 2010, v. 19, n. 8, p. 1479, doi. 10.1093/hmg/ddq022
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- Article
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma.
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- Human Molecular Genetics, 2006, v. 15, n. 18, p. 2682, doi. 10.1093/hmg/ddl199
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- Article
On the Xq13 Breakpoint: Clinical and Cytogenetic Observations in a Patient with Acute Myelogenous Leukemia.
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- Acta Haematologica, 1983, v. 70, n. 2, p. 134, doi. 10.1159/000206707
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- Article
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect.
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- Genes, Chromosomes & Cancer, 2001, v. 32, n. 3, p. 195, doi. 10.1002/gcc.1183
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- Article
Mutation screening of the CDKN2A promoter in melanoma families.
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- Genes, Chromosomes & Cancer, 2000, v. 28, n. 1, p. 45, doi. 10.1002/(SICI)1098-2264(200005)28:1<45::AID-GCC6>3.0.CO;2-F
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- Article
Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the p53 PIN3 A2-Pro72 Haplotype.
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- Digestion, 2006, v. 74, n. 3/4, p. 228, doi. 10.1159/000100966
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- Article
Genome-wide association study identifies three new melanoma susceptibility loci.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1108, doi. 10.1038/ng.959
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- Article
Genome-wide association study identifies three loci associated with melanoma risk.
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- Nature Genetics, 2009, v. 41, n. 8, p. 920, doi. 10.1038/ng.411
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- Article
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length.
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- JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 10, p. 1, doi. 10.1093/jnci/dju267
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- Article
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length.
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- JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 10, p. 1, doi. 10.1093/jnci/dju267
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- Article
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.
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- Familial Cancer, 2012, v. 11, n. 3, p. 411, doi. 10.1007/s10689-012-9529-3
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- Article
Novel PTCH1 Mutations in Patients with Keratocystic Odontogenic Tumors Screened for Nevoid Basal Cell Carcinoma (NBCC) Syndrome.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043827
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- Article
A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer.
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- Endocrine (1355008X), 2016, v. 53, n. 3, p. 672, doi. 10.1007/s12020-015-0720-9
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- Article
The CDKN2A/p16 <sup> INK</sup><sup> 4a</sup> 5′ UTR sequence and translational regulation: impact of novel variants predisposing to melanoma.
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- Pigment Cell & Melanoma Research, 2016, v. 29, n. 2, p. 210, doi. 10.1111/pcmr.12444
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- Article
Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family.
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- Pigment Cell & Melanoma Research, 2012, v. 25, n. 2, p. 243, doi. 10.1111/j.1755-148X.2012.00969.x
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- Article
Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.
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- Journal of Cutaneous Pathology, 2012, v. 39, n. 3, p. 366, doi. 10.1111/j.1600-0560.2011.01813.x
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- Article
MDM2 SNP309 genotype influences survival of metastatic but not of localized neuroblastoma.
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- Pediatric Blood & Cancer, 2009, v. 53, n. 4, p. 576, doi. 10.1002/pbc.22132
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- Article
Lactoferrin binding sites and nuclear localization in K562(S) cells.
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- Journal of Cellular Physiology, 1992, v. 153, n. 3, p. 477, doi. 10.1002/jcp.1041530306
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- Article
Effect of endothelial cell conditioned medium on the growth of human bone marrow fibroblasts.
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- Journal of Cellular Physiology, 1985, v. 123, n. 3, p. 343, doi. 10.1002/jcp.1041230308
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- Article
The yeast CDP1 gene encodes a triple-helical DNA-binding protein.
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- Nucleic Acids Research, 2000, v. 28, n. 21, p. 4090, doi. 10.1093/nar/28.21.4090
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- Article
Coexisting NRAS and BRAF Mutations in Primary Familial Melanomas with Specific CDKN2A Germline Alterations.
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- Journal of Investigative Dermatology, 2010, v. 130, n. 2, p. 618, doi. 10.1038/jid.2009.287
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- Article
CDKN2 A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment.
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- Human Mutation, 2014, v. 35, n. 7, p. 828, doi. 10.1002/humu.22550
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- Article
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
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- International Journal of Cancer, 2015, v. 136, n. 6, p. 1351, doi. 10.1002/ijc.29099
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- Article