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Double-gradient DGGE for optimized detection of DNA point mutations.
Cremonesi L, Firpo S, Ferrari M, Righetti PG, Gelfi C. Cremonesi L, et al. Biotechniques. 1997 Feb;22(2):326-30. doi: 10.2144/97222rr01. Biotechniques. 1997. PMID: 9043706
High-throughput mutational screening for beta-thalassemia by single-nucleotide extension.
Galbiati S, Chiari M, Macellari M, Ferrari M, Cremonesi L, Cretich M. Galbiati S, et al. Electrophoresis. 2007 Dec;28(23):4289-94. doi: 10.1002/elps.200700181. Electrophoresis. 2007. PMID: 18040987
COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
Galbiati S, Monguzzi A, Damin F, Soriani N, Passiu M, Castellani C, Natacci F, Curcio C, Seia M, Lalatta F, Chiari M, Ferrari M, Cremonesi L. Galbiati S, et al. J Med Genet. 2016 Jul;53(7):481-7. doi: 10.1136/jmedgenet-2015-103229. Epub 2016 Feb 24. J Med Genet. 2016. PMID: 26912453
Dual-color microchip electrophoresis with single-photon avalanche diodes: application to mutation detection.
Stenirri S, Cretich M, Rech I, Restelli A, Ghioni M, Cova S, Ferrari M, Cremonesi L, Chiari M. Stenirri S, et al. Electrophoresis. 2008 Dec;29(24):4972-5. doi: 10.1002/elps.200800323. Electrophoresis. 2008. PMID: 19130576
Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.
Galbiati S, Foglieni B, Travi M, Curcio C, Restagno G, Sbaiz L, Smid M, Pasi F, Ferrari A, Ferrari M, Cremonesi L. Galbiati S, et al. Haematologica. 2008 Apr;93(4):610-4. doi: 10.3324/haematol.11895. Epub 2008 Mar 6. Haematologica. 2008. PMID: 18326525
Fetal DNA detection in maternal plasma throughout gestation.
Galbiati S, Smid M, Gambini D, Ferrari A, Restagno G, Viora E, Campogrande M, Bastonero S, Pagliano M, Calza S, Ferrari M, Cremonesi L. Galbiati S, et al. Hum Genet. 2005 Jul;117(2-3):243-8. doi: 10.1007/s00439-005-1330-z. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906093
Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.
Cremonesi L, Foglieni B, Fermo I, Cozzi A, Paroni R, Ruggeri G, Belloli S, Levi S, Fargion S, Ferrari M, Arosio P. Cremonesi L, et al. Haematologica. 2003 Oct;88(10):1110-6. Haematologica. 2003. PMID: 14555306
BACKGROUND AND OBJECTIVES: Hereditary hyperferritinemia cataract syndrome is caused by mutations of the iron responsive elements (IREs) of L-ferritin mRNA. These alter the IRE structure and determine L-ferritin upregulation. IREs are located in 5'untranslated region …
BACKGROUND AND OBJECTIVES: Hereditary hyperferritinemia cataract syndrome is caused by mutations of the iron responsive elements (IREs) of …
Fetal DNA in maternal plasma in twin pregnancies.
Smid M, Galbiati S, Vassallo A, Gambini D, Ferrari A, Restagno G, Viora E, Pagliano M, Calza S, Ferrari M, Cremonesi L. Smid M, et al. Clin Chem. 2003 Sep;49(9):1526-8. doi: 10.1373/49.9.1526. Clin Chem. 2003. PMID: 12928237 No abstract available.
Denaturing HPLC analysis of DNA deletions and insertions.
Cremonesi L, Stenirri S, Fermo I, Paroni R, Ferrari M, Cazzola M, Arosio P. Cremonesi L, et al. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600
Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator gene.
Mari C, Bruno F, Galbiati S, Torri A, Lombardo F, Seia M, Ferrari M, Restagno G, Cremonesi L. Mari C, et al. Clin Chem Lab Med. 2009;47(9):1051-4. doi: 10.1515/CCLM.2009.262. Clin Chem Lab Med. 2009. PMID: 19728845
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