Found: 18
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Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 1, p. 65, doi. 10.1111/cge.12040
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- Article
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas.
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- Clinical Genetics, 2009, v. 76, n. 5, p. 481, doi. 10.1111/j.1399-0004.2009.01259.x
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- Article
Combining germline, tissue and liquid biopsy analysis by comprehensive genomic profiling to improve the yield of actionable variants in a real-world cancer cohort.
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- Journal of Translational Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12967-024-05227-2
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- Article
Long-Term Treatment of Congestive Heart Failure with Oral Ibopamine.
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- Cardiology, 1990, v. 77, n. S5, p. 43, doi. 10.1159/000174695
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- Article
The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-β production.
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- 2007
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- Correction Notice
Data Modeling for Tools and Technologies for the Analysis and Synthesis of NANOstructures (TASNANO) Project.
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- Journal of Information Technology Research, 2009, v. 2, n. 3, p. 49, doi. 10.4018/jitr.2009070104
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- Publication type:
- Article
Coherent X-ray diffraction imaging of nanoengineered polymeric capsules.
- Published in:
- JETP Letters, 2017, v. 106, n. 8, p. 540, doi. 10.1134/S0021364017200036
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- Article
(+)-MCPG induces PKCε translocation in cortical synaptosomes through a PLD-coupled mGluR.
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- European Journal of Neuroscience, 2000, v. 12, n. 4, p. 1310, doi. 10.1046/j.1460-9568.2000.00023.x
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- Article
CaMKII-dependent phosphorylation of NR2A and NR2B is decreased in animals characterized by hippocampal damage and impaired LTP.
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- European Journal of Neuroscience, 1999, v. 11, n. 1, p. 141, doi. 10.1046/j.1460-9568.1999.00414.x
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- Publication type:
- Article
High‐ and intermediate‐risk susceptibility variants in melanoma families from the Mediterranean area: A multicentre cohort from the MelaNostrum Consortium.
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- Journal of the European Academy of Dermatology & Venereology, 2023, v. 37, n. 12, p. 2498, doi. 10.1111/jdv.19461
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- Article
Melanoma in children and adolescents: analysis of susceptibility genes in 123 Italian patients.
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- Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 2, p. 213, doi. 10.1111/jdv.17735
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- Article
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.
- Published in:
- Familial Cancer, 2012, v. 11, n. 1, p. 41, doi. 10.1007/s10689-011-9483-5
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- Article
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome.
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- Familial Cancer, 2009, v. 8, n. 4, p. 547, doi. 10.1007/s10689-009-9285-1
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- Publication type:
- Article
Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
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- Human Mutation, 2005, v. 25, n. 3, p. 322, doi. 10.1002/humu.9317
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- Article
Prevalence of the E318 K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.
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- Pigment Cell & Melanoma Research, 2013, v. 26, n. 2, p. 259, doi. 10.1111/pcmr.12047
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- Publication type:
- Article
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
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- Pigment Cell & Melanoma Research, 2008, v. 21, n. 6, p. 700, doi. 10.1111/j.1755-148X.2008.00512.x
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- Publication type:
- Article
Increased Secretion of the Amino-Terminal Fragment of Amyloid Precursor Protein in Brains of Rats with a Constitutive Up-Regulation of Protein Kinase C.
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- Journal of Neurochemistry, 1997, v. 68, n. 6, p. 2523, doi. 10.1046/j.1471-4159.1997.68062523.x
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- Article
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis.
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- Child: Care, Health & Development, 2005, v. 31, n. 3, p. 351, doi. 10.1111/j.1365-2214.2005.00514.x
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- Publication type:
- Article