Search research articles
Contact Us
Filters
Showing results (151-160 of 202) with videos related to
Page
of 21
Sort By:
Journal of Clinical Periodontology
|
August 20, 2025
Developing Predictive Models for Periodontitis Progression Using Artificial Intelligence: A Longitudinal Cohort Study
Camila Pinheiro Furquim, Lannawill Caruth, Ganesh Chandrasekaran, et al.
Journal of Medical Genetics
|
June 5, 2010
Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer
Michael S Nahorski, Derek H K Lim, Lynn Martin, et al.
Human Molecular Genetics
|
March 27, 2013
DNA polymerase ε and δ exonuclease domain mutations in endometrial cancer
David N Church, Sarah E W Briggs, Claire Palles, et al.
Frontiers in Psychiatry
|
February 21, 2020
The interRAI Suite of Mental Health Assessment Instruments: An Integrated System for the Continuum of Care
John P Hirdes, Coline van Everdingen, Jason Ferris, et al.
Cancer Research
|
May 19, 2006
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
Zoe E Kemp, Luis G Carvajal-Carmona, Ella Barclay, et al.
Nature Communications
|
June 28, 2023
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Nature Communications
|
June 19, 2023
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Human Molecular Genetics
|
August 23, 2006
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan
Zoe Kemp, Luis Carvajal-Carmona, Sarah Spain, et al.
Endocrine-Related Cancer
|
August 21, 2015
The 8q24 rs6983267G variant is associated with increased thyroid cancer risk
Ruta Sahasrabudhe, Ana Estrada, Paul Lott, et al.
Nature Genetics
|
October 1, 2021
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
Philip S Robinson, Tim H H Coorens, Claire Palles, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 202) with videos related to
Sort By:
Page
of 21
Journal of Clinical Periodontology
|
August 20, 2025
Developing Predictive Models for Periodontitis Progression Using Artificial Intelligence: A Longitudinal Cohort Study
Camila Pinheiro Furquim, Lannawill Caruth, Ganesh Chandrasekaran, et al.
Journal of Medical Genetics
|
June 5, 2010
Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer
Michael S Nahorski, Derek H K Lim, Lynn Martin, et al.
Human Molecular Genetics
|
March 27, 2013
DNA polymerase ε and δ exonuclease domain mutations in endometrial cancer
David N Church, Sarah E W Briggs, Claire Palles, et al.
Frontiers in Psychiatry
|
February 21, 2020
The interRAI Suite of Mental Health Assessment Instruments: An Integrated System for the Continuum of Care
John P Hirdes, Coline van Everdingen, Jason Ferris, et al.
Cancer Research
|
May 19, 2006
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
Zoe E Kemp, Luis G Carvajal-Carmona, Ella Barclay, et al.
Nature Communications
|
June 28, 2023
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Nature Communications
|
June 19, 2023
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Human Molecular Genetics
|
August 23, 2006
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan
Zoe Kemp, Luis Carvajal-Carmona, Sarah Spain, et al.
Endocrine-Related Cancer
|
August 21, 2015
The 8q24 rs6983267G variant is associated with increased thyroid cancer risk
Ruta Sahasrabudhe, Ana Estrada, Paul Lott, et al.
Nature Genetics
|
October 1, 2021
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
Philip S Robinson, Tim H H Coorens, Claire Palles, et al.
Page
of 21