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I Ceccherini

Showing results (21-30 of 80) 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.
Genomics|June 1, 1997
Genomic structure of the human lysosomal alpha-mannosidase gene (MANB)H M Riise, T Berg, O Nilssen, et al.
American Journal of Human Genetics|February 1, 1991
Saturating the region of the polycystic kidney disease gene with NotI linking clonesH Himmelbauer, G G Germino, I Ceccherini, et al.
Mutation Research|June 1, 1993
Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donorsH Steingrimsdottir, G Rowley, A Waugh, et al.
Human Molecular Genetics|November 1, 1995
Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) ratI Ceccherini, A L Zhang, I Matera, et al.
Annals of Human Genetics|January 31, 2006
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of allelesF Lantieri, P Griseri, F Puppo, et al.
Journal of Endocrinological Investigation|March 1, 1994
Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosisI Ceccherini, C Romei, V Barone, et al.
Clinical Genetics|September 12, 2017
Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutationM Di Rocco, M Rusmini, F Caroli, et al.
Molecular and Cellular Biology|September 21, 2001
The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosisB Mograbi, R Bocciardi, I Bourget, et al.
Prenatal Diagnosis|November 1, 1989
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeksI Ceccherini, M Lituania, M S Cordone, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
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.
Genomics|June 1, 1997
Genomic structure of the human lysosomal alpha-mannosidase gene (MANB)H M Riise, T Berg, O Nilssen, et al.
American Journal of Human Genetics|February 1, 1991
Saturating the region of the polycystic kidney disease gene with NotI linking clonesH Himmelbauer, G G Germino, I Ceccherini, et al.
Mutation Research|June 1, 1993
Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donorsH Steingrimsdottir, G Rowley, A Waugh, et al.
Human Molecular Genetics|November 1, 1995
Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) ratI Ceccherini, A L Zhang, I Matera, et al.
Annals of Human Genetics|January 31, 2006
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of allelesF Lantieri, P Griseri, F Puppo, et al.
Journal of Endocrinological Investigation|March 1, 1994
Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosisI Ceccherini, C Romei, V Barone, et al.
Clinical Genetics|September 12, 2017
Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutationM Di Rocco, M Rusmini, F Caroli, et al.
Molecular and Cellular Biology|September 21, 2001
The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosisB Mograbi, R Bocciardi, I Bourget, et al.
Prenatal Diagnosis|November 1, 1989
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeksI Ceccherini, M Lituania, M S Cordone, et al.
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