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I Ceccherini

Showing results (41-50 of 80) with videos related to

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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.
Journal of Medical Genetics|July 7, 2000
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervationM Costa, M Fava, M Seri, et al.
Laboratory Animals|July 19, 2003
The Ret proto-oncogene in the WAG/Rij rat strain: an animal model for inherited C-cell carcinoma?M De Miguel, J M Fernández-Santos, I Trigo-Sánchez, et al.
Human Molecular Genetics|November 1, 1993
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung diseaseY Luo, I Ceccherini, B Pasini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Rat models of autosomal dominant polycystic kidney diseaseN Gretz, B Kränzlin, R Pey, et al.
Clinical Genetics|March 19, 2010
Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutationS Parodi, C Vollono, M P Baglietto, et al.
Oncogene|March 16, 1995
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogeneI Ceccherini, R M Hofstra, Y Luo, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Frontiers in Genetics|August 23, 2023
Whole genome sequencing in ROHHAD trios proved inconclusive: what's beyond?A Grossi, M Rusmini, R Cusano, et al.
Journal of Medical Genetics|September 10, 2003
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's diseaseM Sancandi, P Griseri, B Pesce, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
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.
Journal of Medical Genetics|July 7, 2000
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervationM Costa, M Fava, M Seri, et al.
Laboratory Animals|July 19, 2003
The Ret proto-oncogene in the WAG/Rij rat strain: an animal model for inherited C-cell carcinoma?M De Miguel, J M Fernández-Santos, I Trigo-Sánchez, et al.
Human Molecular Genetics|November 1, 1993
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung diseaseY Luo, I Ceccherini, B Pasini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Rat models of autosomal dominant polycystic kidney diseaseN Gretz, B Kränzlin, R Pey, et al.
Clinical Genetics|March 19, 2010
Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutationS Parodi, C Vollono, M P Baglietto, et al.
Oncogene|March 16, 1995
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogeneI Ceccherini, R M Hofstra, Y Luo, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Frontiers in Genetics|August 23, 2023
Whole genome sequencing in ROHHAD trios proved inconclusive: what's beyond?A Grossi, M Rusmini, R Cusano, et al.
Journal of Medical Genetics|September 10, 2003
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's diseaseM Sancandi, P Griseri, B Pesce, et al.
Pageof 8