Search research articles
Contact Us
Filters
Showing results (41-50 of 228) with videos related to
Page
of 23
Sort By:
BMC Cancer
|
May 15, 2010
Expression analysis of genes associated with human osteosarcoma tumors shows correlation of RUNX2 overexpression with poor response to chemotherapy
Bekim Sadikovic, Paul Thorner, Susan Chilton-Macneill, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 4, 2020
Genetic Testing in Children with Epilepsy: Report of a Single-Center Experience
So Lee, Natalya Karp, Eugenio Zapata-Aldana, et al.
Oncogene
|
December 3, 2003
Characterization of functional elements in the neurofibromatosis (NF1) proximal promoter region
Min-Xu Zou, Darci T Butcher, Bekim Sadikovic, et al.
Breast Cancer Research : BCR
|
July 22, 2008
Epigenetic mapping and functional analysis in a breast cancer metastasis model using whole-genome promoter tiling microarrays
David I Rodenhiser, Joseph Andrews, Wendy Kennette, et al.
The Journal of Molecular Diagnostics : JMD
|
September 2, 2016
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C Schenkel, Charles Schwartz, Cindy Skinner, et al.
Scientific Reports
|
April 27, 2018
MALAT1: An Epigenetic Regulator of Inflammation in Diabetic Retinopathy
Saumik Biswas, Anu Alice Thomas, Shali Chen, et al.
Frontiers in Oncology
|
May 10, 2018
Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues
Erfan Aref-Eshghi, Laila C Schenkel, Peter Ainsworth, et al.
Neuromuscular Disorders : NMD
|
December 26, 2022
The discovery of the DNA methylation episignature for Duchenne muscular dystrophy
Leighton Schreyer, Jack Reilly, Haley McConkey, et al.
Clinical Epigenetics
|
January 12, 2025
Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature
Jan Fischer, Mariëlle Alders, Marcel M A M Mannens, et al.
Journal of Medical Genetics
|
May 8, 2020
Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients
Michael Volodarsky, Jennifer Kerkhof, Alan Stuart, et al.
Page
of 23
Search research articles
Search
Showing results (41-50 of 228) with videos related to
Sort By:
Page
of 23
BMC Cancer
|
May 15, 2010
Expression analysis of genes associated with human osteosarcoma tumors shows correlation of RUNX2 overexpression with poor response to chemotherapy
Bekim Sadikovic, Paul Thorner, Susan Chilton-Macneill, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 4, 2020
Genetic Testing in Children with Epilepsy: Report of a Single-Center Experience
So Lee, Natalya Karp, Eugenio Zapata-Aldana, et al.
Oncogene
|
December 3, 2003
Characterization of functional elements in the neurofibromatosis (NF1) proximal promoter region
Min-Xu Zou, Darci T Butcher, Bekim Sadikovic, et al.
Breast Cancer Research : BCR
|
July 22, 2008
Epigenetic mapping and functional analysis in a breast cancer metastasis model using whole-genome promoter tiling microarrays
David I Rodenhiser, Joseph Andrews, Wendy Kennette, et al.
The Journal of Molecular Diagnostics : JMD
|
September 2, 2016
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C Schenkel, Charles Schwartz, Cindy Skinner, et al.
Scientific Reports
|
April 27, 2018
MALAT1: An Epigenetic Regulator of Inflammation in Diabetic Retinopathy
Saumik Biswas, Anu Alice Thomas, Shali Chen, et al.
Frontiers in Oncology
|
May 10, 2018
Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues
Erfan Aref-Eshghi, Laila C Schenkel, Peter Ainsworth, et al.
Neuromuscular Disorders : NMD
|
December 26, 2022
The discovery of the DNA methylation episignature for Duchenne muscular dystrophy
Leighton Schreyer, Jack Reilly, Haley McConkey, et al.
Clinical Epigenetics
|
January 12, 2025
Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature
Jan Fischer, Mariëlle Alders, Marcel M A M Mannens, et al.
Journal of Medical Genetics
|
May 8, 2020
Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients
Michael Volodarsky, Jennifer Kerkhof, Alan Stuart, et al.
Page
of 23