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The Journal of Molecular Diagnostics : JMD
|
June 29, 2011
Comparison of allelic discrimination by dHPLC, HRM, and TaqMan in the detection of BRAF mutation V600E
Pablo Carbonell, María C Turpin, Daniel Torres-Moreno, et al.
Magnetic Resonance in Chemistry : MRC
|
March 31, 2007
Solid-state 13C NMR and quantum chemical investigation of metal diene complexes
Zhiru Ma, Julio C Facelli, Ronald J Pugmire, et al.
Annals of Neurology
|
May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA gene
R Navon, R Khosravi, J Melki, et al.
Clinical Genetics
|
June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease
S Andrew, J Theilmann, E Almqvist, et al.
Infection and Immunity
|
July 1, 1997
Rickettsia rickettsii infection of cultured human endothelial cells induces NF-kappaB activation
L A Sporn, S K Sahni, N B Lerner, et al.
Neurology
|
March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotype
R Navon, R Khosravi, T Korczyn, et al.
Presse Medicale (Paris, France : 1983)
|
October 7, 1989
[Value of the early diagnosis of cerebral metastasis in non-small cell lung cancers]
L Demange, L Tack, C Cossart, et al.
Clinical Epigenetics
|
November 11, 2018
Two histologically colorectal carcinomas subsets from the serrated pathway show different methylome signatures and diagnostic biomarkers
José García-Solano, María C Turpin, Daniel Torres-Moreno, et al.
Neurology
|
January 1, 1990
Adult sphingomyelinase deficiency: report of 2 patients who initially presented with psychiatric disorders
G Dubois, J M Mussini, M Auclair, et al.
Journal of Biological Regulators and Homeostatic Agents
|
March 16, 2013
Three novel human sporadic melanoma cell lines: signaling pathways controlled by MC1R, BRAF and β-catenins
P Zanna, I Maida, C Grieco, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
The Journal of Molecular Diagnostics : JMD
|
June 29, 2011
Comparison of allelic discrimination by dHPLC, HRM, and TaqMan in the detection of BRAF mutation V600E
Pablo Carbonell, María C Turpin, Daniel Torres-Moreno, et al.
Magnetic Resonance in Chemistry : MRC
|
March 31, 2007
Solid-state 13C NMR and quantum chemical investigation of metal diene complexes
Zhiru Ma, Julio C Facelli, Ronald J Pugmire, et al.
Annals of Neurology
|
May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA gene
R Navon, R Khosravi, J Melki, et al.
Clinical Genetics
|
June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease
S Andrew, J Theilmann, E Almqvist, et al.
Infection and Immunity
|
July 1, 1997
Rickettsia rickettsii infection of cultured human endothelial cells induces NF-kappaB activation
L A Sporn, S K Sahni, N B Lerner, et al.
Neurology
|
March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotype
R Navon, R Khosravi, T Korczyn, et al.
Presse Medicale (Paris, France : 1983)
|
October 7, 1989
[Value of the early diagnosis of cerebral metastasis in non-small cell lung cancers]
L Demange, L Tack, C Cossart, et al.
Clinical Epigenetics
|
November 11, 2018
Two histologically colorectal carcinomas subsets from the serrated pathway show different methylome signatures and diagnostic biomarkers
José García-Solano, María C Turpin, Daniel Torres-Moreno, et al.
Neurology
|
January 1, 1990
Adult sphingomyelinase deficiency: report of 2 patients who initially presented with psychiatric disorders
G Dubois, J M Mussini, M Auclair, et al.
Journal of Biological Regulators and Homeostatic Agents
|
March 16, 2013
Three novel human sporadic melanoma cell lines: signaling pathways controlled by MC1R, BRAF and β-catenins
P Zanna, I Maida, C Grieco, et al.
Page
of 12