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Neurogenetics
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October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis
K Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
August 19, 2009
Differential expression of biomarkers in primary non-small cell lung cancer and metastatic sites
Carlos Gomez-Roca, Christophe M Raynaud, Frederique Penault-Llorca, et al.
Clinical Genetics
|
January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A gene
M-P Moizard, N Ronce, S Blesson, et al.
International Journal of Cancer
|
August 21, 2010
Tumor associated mesenchymal stem cells protects ovarian cancer cells from hyperthermia through CXCL12
Raphael Lis, Cyril Touboul, Pejman Mirshahi, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
June 11, 2022
The immune landscape of solid pediatric tumors
Shimaa Sherif, Jessica Roelands, William Mifsud, et al.
Molecular Psychiatry
|
February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism
F Laumonnier, C Shoubridge, C Antar, et al.
Journal of Proteome Research
|
June 6, 2013
Adaptation of a commonly used, chemically defined medium for human embryonic stem cells to stable isotope labeling with amino acids in cell culture
Albert R Liberski, Muna N Al-Noubi, Zahra H Rahman, et al.
Frontiers in Oncology
|
February 23, 2026
Enhancing the accuracy of molecular classification of pediatric CNS tumors: a dual-classifier approach using DNA methylation profiling
Esra Moosa, Rania Alanany, Shimaa Sherif, et al.
Behavior Genetics
|
January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families
M Huc-Chabrolle, C Charon, A Guilmatre, et al.
The Journal of Allergy and Clinical Immunology
|
May 16, 2024
Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration
Fang Yu, Satanay Hubrack, Christophe M Raynaud, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 64) with videos related to
Sort By:
Page
of 7
Neurogenetics
|
October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis
K Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
August 19, 2009
Differential expression of biomarkers in primary non-small cell lung cancer and metastatic sites
Carlos Gomez-Roca, Christophe M Raynaud, Frederique Penault-Llorca, et al.
Clinical Genetics
|
January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A gene
M-P Moizard, N Ronce, S Blesson, et al.
International Journal of Cancer
|
August 21, 2010
Tumor associated mesenchymal stem cells protects ovarian cancer cells from hyperthermia through CXCL12
Raphael Lis, Cyril Touboul, Pejman Mirshahi, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
June 11, 2022
The immune landscape of solid pediatric tumors
Shimaa Sherif, Jessica Roelands, William Mifsud, et al.
Molecular Psychiatry
|
February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism
F Laumonnier, C Shoubridge, C Antar, et al.
Journal of Proteome Research
|
June 6, 2013
Adaptation of a commonly used, chemically defined medium for human embryonic stem cells to stable isotope labeling with amino acids in cell culture
Albert R Liberski, Muna N Al-Noubi, Zahra H Rahman, et al.
Frontiers in Oncology
|
February 23, 2026
Enhancing the accuracy of molecular classification of pediatric CNS tumors: a dual-classifier approach using DNA methylation profiling
Esra Moosa, Rania Alanany, Shimaa Sherif, et al.
Behavior Genetics
|
January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families
M Huc-Chabrolle, C Charon, A Guilmatre, et al.
The Journal of Allergy and Clinical Immunology
|
May 16, 2024
Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration
Fang Yu, Satanay Hubrack, Christophe M Raynaud, et al.
Page
of 7