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Nature Communications
|
September 22, 2020
Telomere dysfunction activates YAP1 to drive tissue inflammation
Deepavali Chakravarti, Baoli Hu, Xizeng Mao, et al.
Journal of the National Cancer Institute
|
December 9, 2014
Germline mutations in shelterin complex genes are associated with familial glioma
Matthew N Bainbridge, Georgina N Armstrong, M Monica Gramatges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies
Bo Yuan, Juanita Neira, Davut Pehlivan, et al.
Angiogenesis
|
September 1, 2018
Understanding the evolving phenotype of vascular complications in telomere biology disorders
Cecilia Higgs, Yanick J Crow, Denise M Adams, et al.
The Journal of Clinical Investigation
|
April 3, 2025
ATM-dependent DNA damage response constrains cell growth and drives clonal hematopoiesis in telomere biology disorders
Christopher M Sande, Stone Chen, Dana V Mitchell, et al.
American Journal of Human Genetics
|
February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
Lindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
The Journal of Allergy and Clinical Immunology
|
September 1, 2016
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
Asbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
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Showing results (71-80 of 77) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 77 results.
Nature Communications
|
September 22, 2020
Telomere dysfunction activates YAP1 to drive tissue inflammation
Deepavali Chakravarti, Baoli Hu, Xizeng Mao, et al.
Journal of the National Cancer Institute
|
December 9, 2014
Germline mutations in shelterin complex genes are associated with familial glioma
Matthew N Bainbridge, Georgina N Armstrong, M Monica Gramatges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies
Bo Yuan, Juanita Neira, Davut Pehlivan, et al.
Angiogenesis
|
September 1, 2018
Understanding the evolving phenotype of vascular complications in telomere biology disorders
Cecilia Higgs, Yanick J Crow, Denise M Adams, et al.
The Journal of Clinical Investigation
|
April 3, 2025
ATM-dependent DNA damage response constrains cell growth and drives clonal hematopoiesis in telomere biology disorders
Christopher M Sande, Stone Chen, Dana V Mitchell, et al.
American Journal of Human Genetics
|
February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
Lindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
The Journal of Allergy and Clinical Immunology
|
September 1, 2016
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
Asbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
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of 8