Search research articles
Contact Us
Filters
Showing results (101-110 of 109) with videos related to
Page
of 11
Sort By:
You have reached the last page of results.
This site can display upto 109 results.
BMC Public Health
|
October 1, 2025
Awareness, facilitators, barriers, and behaviours surrounding brain health: a large-scale cross-sectional survey of adults across UK and Ireland
R F Townsend, O M Shannon, E Stevenson, et al.
Nature Aging
|
April 28, 2023
Recruitment of inflammatory monocytes by senescent fibroblasts inhibits antigen-specific tissue immunity during human aging
Emma S Chambers, Milica Vukmanovic-Stejic, Barbara B Shih, et al.
Aging Cell
|
October 18, 2024
Multiple outcomes of the germline p16<sup>INK4a</sup> mutation affecting senescence and immunity in human skin
Priya Subramanian, Souraya Sayegh, Phatthamon Laphanuwat, et al.
Frontiers in Immunology
|
January 22, 2019
Circulating Senescent T Cells Are Linked to Systemic Inflammation and Lesion Size During Human Cutaneous Leishmaniasis
Luciana P Covre, Régia F Martins, Oliver P Devine, et al.
Neurology. Genetics
|
April 8, 2024
Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy
Kun Leng, Cathryn R Cadwell, Walter P Devine, et al.
Nature Communications
|
June 5, 2019
Senescent cells evade immune clearance via HLA-E-mediated NK and CD8<sup>+</sup> T cell inhibition
Branca I Pereira, Oliver P Devine, Milica Vukmanovic-Stejic, et al.
World Neurosurgery
|
February 17, 2024
Modafinil Therapy and Mental Status Following Aneurysmal Subarachnoid Hemorrhage: Comprehensive Stroke Center Analysis
Stefan W Koester, Kavelin Rumalla, Joshua S Catapano, et al.
Human Mutation
|
May 4, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder
Justin O Szot, Anne Slavotinek, Karen Chong, et al.
American Journal of Human Genetics
|
November 9, 2022
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis
Christin S Adamo, Aude Beyens, Alvise Schiavinato, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 109 results.
BMC Public Health
|
October 1, 2025
Awareness, facilitators, barriers, and behaviours surrounding brain health: a large-scale cross-sectional survey of adults across UK and Ireland
R F Townsend, O M Shannon, E Stevenson, et al.
Nature Aging
|
April 28, 2023
Recruitment of inflammatory monocytes by senescent fibroblasts inhibits antigen-specific tissue immunity during human aging
Emma S Chambers, Milica Vukmanovic-Stejic, Barbara B Shih, et al.
Aging Cell
|
October 18, 2024
Multiple outcomes of the germline p16<sup>INK4a</sup> mutation affecting senescence and immunity in human skin
Priya Subramanian, Souraya Sayegh, Phatthamon Laphanuwat, et al.
Frontiers in Immunology
|
January 22, 2019
Circulating Senescent T Cells Are Linked to Systemic Inflammation and Lesion Size During Human Cutaneous Leishmaniasis
Luciana P Covre, Régia F Martins, Oliver P Devine, et al.
Neurology. Genetics
|
April 8, 2024
Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy
Kun Leng, Cathryn R Cadwell, Walter P Devine, et al.
Nature Communications
|
June 5, 2019
Senescent cells evade immune clearance via HLA-E-mediated NK and CD8<sup>+</sup> T cell inhibition
Branca I Pereira, Oliver P Devine, Milica Vukmanovic-Stejic, et al.
World Neurosurgery
|
February 17, 2024
Modafinil Therapy and Mental Status Following Aneurysmal Subarachnoid Hemorrhage: Comprehensive Stroke Center Analysis
Stefan W Koester, Kavelin Rumalla, Joshua S Catapano, et al.
Human Mutation
|
May 4, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder
Justin O Szot, Anne Slavotinek, Karen Chong, et al.
American Journal of Human Genetics
|
November 9, 2022
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis
Christin S Adamo, Aude Beyens, Alvise Schiavinato, et al.
Page
of 11