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Neuro-Oncology
|
February 19, 2010
Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses
Artemis P Vogazianou, Raymond Chan, L Magnus Bäcklund, et al.
Human Genetics
|
August 3, 2013
Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort
Cavin Ward-Caviness, Carol Haynes, Colette Blach, et al.
Journal of the American Heart Association
|
October 24, 2019
Epigenome-Wide Association Study for All-Cause Mortality in a Cardiovascular Cohort Identifies Differential Methylation in Castor Zinc Finger 1 (<i>CASZ1</i>)
Jawan W Abdulrahim, Lydia Coulter Kwee, Elizabeth Grass, et al.
Aging Cell
|
November 28, 2024
Epigenetic age acceleration predicts subject-specific white matter degeneration in the human brain
Benjamin T Newman, Joshua S Danoff, Morgan E Lynch, et al.
Diabetes
|
October 29, 2002
Linkage and association with type 1 diabetes on chromosome 1q42
Kathryn G Ewens, Lindsey N Johnson, Beth Wapelhorst, et al.
Annals of Human Genetics
|
December 24, 2013
Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation
Christina A Markunas, David S Enterline, Kaitlyn Dunlap, et al.
Acta Neuropathologica Communications
|
June 27, 2024
Publisher Correction: Ganglioglioma deep transcriptomics reveals primitive neuroectoderm neural precursor‑like population
Joshua A Regal, María E Guerra García, Vaibhav Jain, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
UBE2N is essential for maintenance of skin homeostasis and suppression of inflammation
Min Jin Lee, Manel Ben Hammouda, Wanying Miao, et al.
Acta Neuropathologica Communications
|
April 22, 2024
Spatial transcriptomics reveals segregation of tumor cell states in glioblastoma and marked immunosuppression within the perinecrotic niche
Mengyi Liu, Zhicheng Ji, Vaibhav Jain, et al.
Plos One
|
April 27, 2013
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates
Christina A Markunas, Karen Soldano, Kaitlyn Dunlap, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 142) with videos related to
Sort By:
Page
of 15
Neuro-Oncology
|
February 19, 2010
Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses
Artemis P Vogazianou, Raymond Chan, L Magnus Bäcklund, et al.
Human Genetics
|
August 3, 2013
Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort
Cavin Ward-Caviness, Carol Haynes, Colette Blach, et al.
Journal of the American Heart Association
|
October 24, 2019
Epigenome-Wide Association Study for All-Cause Mortality in a Cardiovascular Cohort Identifies Differential Methylation in Castor Zinc Finger 1 (<i>CASZ1</i>)
Jawan W Abdulrahim, Lydia Coulter Kwee, Elizabeth Grass, et al.
Aging Cell
|
November 28, 2024
Epigenetic age acceleration predicts subject-specific white matter degeneration in the human brain
Benjamin T Newman, Joshua S Danoff, Morgan E Lynch, et al.
Diabetes
|
October 29, 2002
Linkage and association with type 1 diabetes on chromosome 1q42
Kathryn G Ewens, Lindsey N Johnson, Beth Wapelhorst, et al.
Annals of Human Genetics
|
December 24, 2013
Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation
Christina A Markunas, David S Enterline, Kaitlyn Dunlap, et al.
Acta Neuropathologica Communications
|
June 27, 2024
Publisher Correction: Ganglioglioma deep transcriptomics reveals primitive neuroectoderm neural precursor‑like population
Joshua A Regal, María E Guerra García, Vaibhav Jain, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
UBE2N is essential for maintenance of skin homeostasis and suppression of inflammation
Min Jin Lee, Manel Ben Hammouda, Wanying Miao, et al.
Acta Neuropathologica Communications
|
April 22, 2024
Spatial transcriptomics reveals segregation of tumor cell states in glioblastoma and marked immunosuppression within the perinecrotic niche
Mengyi Liu, Zhicheng Ji, Vaibhav Jain, et al.
Plos One
|
April 27, 2013
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates
Christina A Markunas, Karen Soldano, Kaitlyn Dunlap, et al.
Page
of 15