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Clinical Genetics
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March 8, 2017
SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly
P Fontana, M Grasso, F Acquaviva, et al.
ACS Applied Materials & Interfaces
|
July 8, 2015
Ultrahigh Aspect Ratio Copper-Nanowire-Based Hybrid Transparent Conductive Electrodes with PEDOT:PSS and Reduced Graphene Oxide Exhibiting Reduced Surface Roughness and Improved Stability
Zhaozhao Zhu, Trent Mankowski, Kaushik Balakrishnan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 28, 1999
Engagement of p75/AIRM1 or CD33 inhibits the proliferation of normal or leukemic myeloid cells
C Vitale, C Romagnani, M Falco, et al.
European Journal of Immunology
|
August 1, 1997
HLA-G recognition by human natural killer cells. Involvement of CD94 both as inhibitory and as activating receptor complex
D Pende, S Sivori, L Accame, et al.
Annals of Ophthalmology
|
November 1, 1992
Markers of vascular injury in Behçet's disease associated with retinal vasculitis
P Pivetti-Pezzi, R Priori, G Catarinelli, et al.
Human Genetics
|
September 12, 2000
Female fetal cells in maternal blood: use of DNA polymorphisms to prove origin
O Samura, B Pertl, S Sohda, et al.
Human Immunology
|
June 1, 1992
Analysis of HLA DP, DQ, and DR alleles in adult Italian rheumatoid arthritis patients
G Angelini, G Morozzi, L Delfino, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
October 1, 1991
Analysis of HLA specificity of human monoclonal antibodies by cytofluorimetry and cell ELISA
M P Pistillo, P L Tazzari, O Mazzoleni, et al.
European Journal of Immunology
|
March 27, 2001
Identification of NKp80, a novel triggering molecule expressed by human NK cells
M Vitale, M Falco, R Castriconi, et al.
European Journal of Medical Genetics
|
January 26, 2010
Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients
L Grillo, S Reitano, G Belfiore, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 102) with videos related to
Sort By:
Page
of 11
Clinical Genetics
|
March 8, 2017
SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly
P Fontana, M Grasso, F Acquaviva, et al.
ACS Applied Materials & Interfaces
|
July 8, 2015
Ultrahigh Aspect Ratio Copper-Nanowire-Based Hybrid Transparent Conductive Electrodes with PEDOT:PSS and Reduced Graphene Oxide Exhibiting Reduced Surface Roughness and Improved Stability
Zhaozhao Zhu, Trent Mankowski, Kaushik Balakrishnan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 28, 1999
Engagement of p75/AIRM1 or CD33 inhibits the proliferation of normal or leukemic myeloid cells
C Vitale, C Romagnani, M Falco, et al.
European Journal of Immunology
|
August 1, 1997
HLA-G recognition by human natural killer cells. Involvement of CD94 both as inhibitory and as activating receptor complex
D Pende, S Sivori, L Accame, et al.
Annals of Ophthalmology
|
November 1, 1992
Markers of vascular injury in Behçet's disease associated with retinal vasculitis
P Pivetti-Pezzi, R Priori, G Catarinelli, et al.
Human Genetics
|
September 12, 2000
Female fetal cells in maternal blood: use of DNA polymorphisms to prove origin
O Samura, B Pertl, S Sohda, et al.
Human Immunology
|
June 1, 1992
Analysis of HLA DP, DQ, and DR alleles in adult Italian rheumatoid arthritis patients
G Angelini, G Morozzi, L Delfino, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
October 1, 1991
Analysis of HLA specificity of human monoclonal antibodies by cytofluorimetry and cell ELISA
M P Pistillo, P L Tazzari, O Mazzoleni, et al.
European Journal of Immunology
|
March 27, 2001
Identification of NKp80, a novel triggering molecule expressed by human NK cells
M Vitale, M Falco, R Castriconi, et al.
European Journal of Medical Genetics
|
January 26, 2010
Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients
L Grillo, S Reitano, G Belfiore, et al.
Page
of 11