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Showing results (11-20 of 49) with videos related to

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Biochemical and Biophysical Research Communications|November 15, 1993
Exon structure and flanking intronic sequences of the human RET proto-oncogeneI Ceccherini, R Bocciardi, Y Luo, et al.
Tumori|September 1, 1996
Malignant pheochromocytoma in multiple endocrine neoplasia type 2B syndrome. Case report and review of the literatureL Scopsi, M R Castellani, M Gullo, et al.
Contributions to Nephrology|November 2, 2001
Search for germline mutations by DGGE in Italian von Hippel-Lindau patientsC Magnani, E Passerini, B Pasini, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2009
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implicationsP Prontera, B Ferrando, V Giuliani, et al.
Journal of Experimental & Clinical Cancer Research : CR|February 15, 2003
BMRI in early detection of breast cancer in patients with increased genetic risk: our preliminary resultsG Trecate, D Vergnaghi, S Bergonzi, et al.
Oncogene|September 22, 1999
The Glu632-Leu633 deletion in cysteine rich domain of Ret induces constitutive dimerization and alters the processing of the receptor proteinI Bongarzone, E Vigano, L Alberti, et al.
Journal of Endocrinological Investigation|July 31, 2010
Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiencyE Napolitano, C Manieri, F Restivo, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 15, 2001
Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumorsS Birindelli, F Perrone, M Oggionni, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Biochemical and Biophysical Research Communications|November 15, 1993
Exon structure and flanking intronic sequences of the human RET proto-oncogeneI Ceccherini, R Bocciardi, Y Luo, et al.
Tumori|September 1, 1996
Malignant pheochromocytoma in multiple endocrine neoplasia type 2B syndrome. Case report and review of the literatureL Scopsi, M R Castellani, M Gullo, et al.
Contributions to Nephrology|November 2, 2001
Search for germline mutations by DGGE in Italian von Hippel-Lindau patientsC Magnani, E Passerini, B Pasini, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2009
A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implicationsP Prontera, B Ferrando, V Giuliani, et al.
Journal of Experimental & Clinical Cancer Research : CR|February 15, 2003
BMRI in early detection of breast cancer in patients with increased genetic risk: our preliminary resultsG Trecate, D Vergnaghi, S Bergonzi, et al.
Oncogene|September 22, 1999
The Glu632-Leu633 deletion in cysteine rich domain of Ret induces constitutive dimerization and alters the processing of the receptor proteinI Bongarzone, E Vigano, L Alberti, et al.
Journal of Endocrinological Investigation|July 31, 2010
Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiencyE Napolitano, C Manieri, F Restivo, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 15, 2001
Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumorsS Birindelli, F Perrone, M Oggionni, et al.
Pageof 5