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Antimicrobial Agents and Chemotherapy
|
January 30, 2013
Complete sequence of the IncT-type plasmid pT-OXA-181 carrying the blaOXA-181 carbapenemase gene from Citrobacter freundii
Laura Villa, Alessandra Carattoli, Patrice Nordmann, et al.
The Journal of Antimicrobial Chemotherapy
|
April 19, 2012
Complete sequencing of an IncH plasmid carrying the blaNDM-1, blaCTX-M-15 and qnrB1 genes
Laura Villa, Laurent Poirel, Patrice Nordmann, et al.
Clinical and Experimental Rheumatology
|
November 26, 2020
One year in review 2020: economic and organisational aspects in rare and complex connective tissue diseases
Sara Cannizzo, Ilaria Palla, Salvatore Pirri, et al.
American Journal of Medical Genetics. Part A
|
April 25, 2013
A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1
Paola Cianci, Valentina Tono, Alessandra Sala, et al.
Antimicrobial Agents and Chemotherapy
|
January 19, 2012
Klebsiella pneumoniae ST258 producing KPC-3 identified in italy carries novel plasmids and OmpK36/OmpK35 porin variants
Aurora García-Fernández, Laura Villa, Claudio Carta, et al.
American Journal of Medical Genetics. Part A
|
September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome
John M Graham, Nancy Kramer, Bassem A Bejjani, et al.
European Journal of Histochemistry : EJH
|
December 16, 2025
The hematopoietic stem cells supportive megakaryocytes as shapers of the bone marrow niche
Francesca Arciprete, Viola Velardi, Paola Verachi, et al.
European Journal of Medical Genetics
|
August 6, 2008
Clinical and molecular characterization of 40 patients with Noonan syndrome
Giovanni Battista Ferrero, Giuseppina Baldassarre, Angelo Giovanni Delmonaco, et al.
Proteins
|
December 21, 2006
Structural and functional effects of disease-causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP-2
Gianfranco Bocchinfuso, Lorenzo Stella, Simone Martinelli, et al.
European Journal of Histochemistry : EJH
|
December 16, 2025
Genetic deletion of P-selectin prevents fibrosis development by inhibiting the neutrophil megakaryocyte emperipolesis in the Gata1<sup>low</sup> mouse model for myelofibrosis
Francesca Arciprete, Viola Velardi, Antonio Di Virgilio, et al.
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Search research articles
Search
Showing results (1-10 of 39) with videos related to
Sort By:
Page
of 4
Antimicrobial Agents and Chemotherapy
|
January 30, 2013
Complete sequence of the IncT-type plasmid pT-OXA-181 carrying the blaOXA-181 carbapenemase gene from Citrobacter freundii
Laura Villa, Alessandra Carattoli, Patrice Nordmann, et al.
The Journal of Antimicrobial Chemotherapy
|
April 19, 2012
Complete sequencing of an IncH plasmid carrying the blaNDM-1, blaCTX-M-15 and qnrB1 genes
Laura Villa, Laurent Poirel, Patrice Nordmann, et al.
Clinical and Experimental Rheumatology
|
November 26, 2020
One year in review 2020: economic and organisational aspects in rare and complex connective tissue diseases
Sara Cannizzo, Ilaria Palla, Salvatore Pirri, et al.
American Journal of Medical Genetics. Part A
|
April 25, 2013
A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1
Paola Cianci, Valentina Tono, Alessandra Sala, et al.
Antimicrobial Agents and Chemotherapy
|
January 19, 2012
Klebsiella pneumoniae ST258 producing KPC-3 identified in italy carries novel plasmids and OmpK36/OmpK35 porin variants
Aurora García-Fernández, Laura Villa, Claudio Carta, et al.
American Journal of Medical Genetics. Part A
|
September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome
John M Graham, Nancy Kramer, Bassem A Bejjani, et al.
European Journal of Histochemistry : EJH
|
December 16, 2025
The hematopoietic stem cells supportive megakaryocytes as shapers of the bone marrow niche
Francesca Arciprete, Viola Velardi, Paola Verachi, et al.
European Journal of Medical Genetics
|
August 6, 2008
Clinical and molecular characterization of 40 patients with Noonan syndrome
Giovanni Battista Ferrero, Giuseppina Baldassarre, Angelo Giovanni Delmonaco, et al.
Proteins
|
December 21, 2006
Structural and functional effects of disease-causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP-2
Gianfranco Bocchinfuso, Lorenzo Stella, Simone Martinelli, et al.
European Journal of Histochemistry : EJH
|
December 16, 2025
Genetic deletion of P-selectin prevents fibrosis development by inhibiting the neutrophil megakaryocyte emperipolesis in the Gata1<sup>low</sup> mouse model for myelofibrosis
Francesca Arciprete, Viola Velardi, Antonio Di Virgilio, et al.
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