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Immunogenetics
|
July 31, 2014
High diversity of MIC genes in non-human primates
Alice Meyer, Raphael Carapito, Louise Ott, et al.
BMC Medical Genetics
|
September 18, 2020
A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report
Arthur Jacob, Jennifer Pasquier, Raphael Carapito, et al.
Genes and Immunity
|
August 8, 2020
A FcɣRIIa polymorphism has a HLA-B57 and HLA-B27 independent effect on HIV disease outcome
Raphael Carapito, Luzia Mayr, Anne Molitor, et al.
Molecular Genetics & Genomic Medicine
|
March 29, 2021
Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant
David Marx, Sophie Caillard, Jérôme Olagne, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2016
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome
Raphael Carapito, Alice Goldenberg, Nicodème Paul, et al.
Iscience
|
February 3, 2025
Endothelial calcium firing mediates the extravasation of metastatic tumor cells
Marina Peralta, Amandine Dupas, Annabel Larnicol, et al.
Immunogenetics
|
May 6, 2015
On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet's disease in an Iranian population
Raphael Carapito, Farhad Shahram, Sandra Michel, et al.
Archives of Dermatological Research
|
April 8, 2025
A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review
Leyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, et al.
Journal of Human Genetics
|
November 15, 2013
A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions
Raphael Carapito, Nicodème Paul, Meiggie Untrau, et al.
Clinical and Experimental Rheumatology
|
January 11, 2021
NKG2D ligands in inflammatory joint diseases: analysis in human samples and mouse models
Alexandre Mariotte, Livio Bernardi, Cécile Macquin, et al.
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of 8
Search research articles
Search
Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
Immunogenetics
|
July 31, 2014
High diversity of MIC genes in non-human primates
Alice Meyer, Raphael Carapito, Louise Ott, et al.
BMC Medical Genetics
|
September 18, 2020
A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report
Arthur Jacob, Jennifer Pasquier, Raphael Carapito, et al.
Genes and Immunity
|
August 8, 2020
A FcɣRIIa polymorphism has a HLA-B57 and HLA-B27 independent effect on HIV disease outcome
Raphael Carapito, Luzia Mayr, Anne Molitor, et al.
Molecular Genetics & Genomic Medicine
|
March 29, 2021
Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant
David Marx, Sophie Caillard, Jérôme Olagne, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2016
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome
Raphael Carapito, Alice Goldenberg, Nicodème Paul, et al.
Iscience
|
February 3, 2025
Endothelial calcium firing mediates the extravasation of metastatic tumor cells
Marina Peralta, Amandine Dupas, Annabel Larnicol, et al.
Immunogenetics
|
May 6, 2015
On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet's disease in an Iranian population
Raphael Carapito, Farhad Shahram, Sandra Michel, et al.
Archives of Dermatological Research
|
April 8, 2025
A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review
Leyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, et al.
Journal of Human Genetics
|
November 15, 2013
A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions
Raphael Carapito, Nicodème Paul, Meiggie Untrau, et al.
Clinical and Experimental Rheumatology
|
January 11, 2021
NKG2D ligands in inflammatory joint diseases: analysis in human samples and mouse models
Alexandre Mariotte, Livio Bernardi, Cécile Macquin, et al.
Page
of 8