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Scientific Reports
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March 7, 2023
Histone H3-wild type diffuse midline gliomas with H3K27me3 loss are a distinct entity with exclusive EGFR or ACVR1 mutation and differential methylation of homeobox genes
Pamela Ajuyah, Chelsea Mayoh, Loretta M S Lau, et al.
Frontiers in Oncology
|
March 20, 2023
<i>In vivo</i> loss of tumorigenicity in a patient-derived orthotopic xenograft mouse model of ependymoma
Jacqueline P Whitehouse, Hilary Hii, Chelsea Mayoh, et al.
Plos One
|
October 11, 2012
qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profiles
Sarah Song, Katia Nones, David Miller, et al.
Human Mutation
|
July 12, 2020
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A)
Simranpreet Kaur, Nicole J Van Bergen, Kristen J Verhey, et al.
Human Mutation
|
April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability
Michael J Field, Raman Kumar, Anna Hackett, et al.
Cancer Biology & Therapy
|
October 10, 2018
Integration of genomics, high throughput drug screening, and personalized xenograft models as a novel precision medicine paradigm for high risk pediatric cancer
Maria Tsoli, Carol Wadham, Mark Pinese, et al.
Cold Spring Harbor Molecular Case Studies
|
April 3, 2019
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Mark J McCabe, Mark Pinese, Chia-Ling Chan, et al.
Cancer
|
October 15, 2014
Clinical and pathologic features of familial pancreatic cancer
Jeremy L Humphris, Amber L Johns, Skye H Simpson, et al.
Oncogene
|
September 24, 2013
c-Myc and Her2 cooperate to drive a stem-like phenotype with poor prognosis in breast cancer
R Nair, D L Roden, W S Teo, et al.
Molecular Genetics & Genomic Medicine
|
January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
Elizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
Page
of 49
Search research articles
Search
Showing results (431-440 of 489) with videos related to
Sort By:
Page
of 49
Scientific Reports
|
March 7, 2023
Histone H3-wild type diffuse midline gliomas with H3K27me3 loss are a distinct entity with exclusive EGFR or ACVR1 mutation and differential methylation of homeobox genes
Pamela Ajuyah, Chelsea Mayoh, Loretta M S Lau, et al.
Frontiers in Oncology
|
March 20, 2023
<i>In vivo</i> loss of tumorigenicity in a patient-derived orthotopic xenograft mouse model of ependymoma
Jacqueline P Whitehouse, Hilary Hii, Chelsea Mayoh, et al.
Plos One
|
October 11, 2012
qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profiles
Sarah Song, Katia Nones, David Miller, et al.
Human Mutation
|
July 12, 2020
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A)
Simranpreet Kaur, Nicole J Van Bergen, Kristen J Verhey, et al.
Human Mutation
|
April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability
Michael J Field, Raman Kumar, Anna Hackett, et al.
Cancer Biology & Therapy
|
October 10, 2018
Integration of genomics, high throughput drug screening, and personalized xenograft models as a novel precision medicine paradigm for high risk pediatric cancer
Maria Tsoli, Carol Wadham, Mark Pinese, et al.
Cold Spring Harbor Molecular Case Studies
|
April 3, 2019
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Mark J McCabe, Mark Pinese, Chia-Ling Chan, et al.
Cancer
|
October 15, 2014
Clinical and pathologic features of familial pancreatic cancer
Jeremy L Humphris, Amber L Johns, Skye H Simpson, et al.
Oncogene
|
September 24, 2013
c-Myc and Her2 cooperate to drive a stem-like phenotype with poor prognosis in breast cancer
R Nair, D L Roden, W S Teo, et al.
Molecular Genetics & Genomic Medicine
|
January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
Elizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
Page
of 49