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M Di Duca

Showing results (1-10 of 11) with videos related to

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FEBS Letters|January 13, 1998
Micro-injection of recombinant lysyl oxidase blocks oncogenic p21-Ha-Ras and progesterone effects on Xenopus laevis oocyte maturationA Di Donato, J C Lacal, M Di Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 19, 2009
Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand geneM Acquila, F Bottini, M DI Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2008
MLPA assay in F8 gene mutation screeningM Acquila, M Pasino, M Di Duca, et al.
Internal Medicine Journal|June 24, 2009
Search for pathogenetic variants of the SPRY2 gene in intestinal innervation defectsS Borghini, M Di Duca, A Pini Prato, et al.
The Journal of Biological Chemistry|August 16, 2000
Lysyl oxidase activates the transcription activity of human collagene III promoter. Possible involvement of Ku antigenM Giampuzzi, G Botti, M Di Duca, et al.
Nephron|January 1, 1997
Lysyl oxidase expression and collagen cross-linking during chronic adriamycin nephropathyA Di Donato, G M Ghiggeri, M Di Duca, 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.
Journal of Medical Genetics|May 4, 2004
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeI Matera, T Bachetti, F Puppo, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
Kidney International|August 11, 2006
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseasesM Di Duca, R Oleggini, S Sanna-Cherchi, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
FEBS Letters|January 13, 1998
Micro-injection of recombinant lysyl oxidase blocks oncogenic p21-Ha-Ras and progesterone effects on Xenopus laevis oocyte maturationA Di Donato, J C Lacal, M Di Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 19, 2009
Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand geneM Acquila, F Bottini, M DI Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2008
MLPA assay in F8 gene mutation screeningM Acquila, M Pasino, M Di Duca, et al.
Internal Medicine Journal|June 24, 2009
Search for pathogenetic variants of the SPRY2 gene in intestinal innervation defectsS Borghini, M Di Duca, A Pini Prato, et al.
The Journal of Biological Chemistry|August 16, 2000
Lysyl oxidase activates the transcription activity of human collagene III promoter. Possible involvement of Ku antigenM Giampuzzi, G Botti, M Di Duca, et al.
Nephron|January 1, 1997
Lysyl oxidase expression and collagen cross-linking during chronic adriamycin nephropathyA Di Donato, G M Ghiggeri, M Di Duca, 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.
Journal of Medical Genetics|May 4, 2004
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeI Matera, T Bachetti, F Puppo, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
Kidney International|August 11, 2006
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseasesM Di Duca, R Oleggini, S Sanna-Cherchi, et al.
Pageof 2