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Violence Against Women
|
March 19, 2025
Are Rape Myths Inherently Gendered? Examining Assumed Gender Ascribed to Gender-Neutral Versions of the Illinois Rape Myth Acceptance Scale Among College Students
Olivia M Kleinsmith, Olivia N Hahn, Dayna Henry, et al.
NPJ Parkinson'S Disease
|
February 29, 2024
Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson's disease phenotypes
Silke Nuber, Xiaoqun Zhang, Thomas D McCaffery, et al.
NPJ Parkinson'S Disease
|
March 13, 2024
Author Correction: Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson's disease phenotypes
Silke Nuber, Xiaoqun Zhang, Thomas D McCaffery, et al.
British Journal of Haematology
|
May 3, 2016
Apparent 'JAK2-negative' polycythaemia vera due to compound mutations in exon 14
Ing Soo Tiong, Debora A Casolari, Sarah Moore, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
August 10, 2010
Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis
King-Hwa Ling, Chelsee A Hewitt, Tim Beissbarth, et al.
Endocrine-Related Cancer
|
March 3, 2012
Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia
Lucia Gagliardi, King-Hwa Ling, Chung H Kok, et al.
Blood Advances
|
April 23, 2025
RBC Transfusion Dependency Refines the Molecular International Prognostic Scoring System for Myelodysplastic Syndrome
Thomas Wiseman, Michaela Spooner, Shreyas Khanna, et al.
BMC Medical Genetics
|
February 19, 2020
Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss
Parvathy Venugopal, Lucia Gagliardi, Cecily Forsyth, et al.
Leukemia
|
October 28, 2015
Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion gene
D M Ross, H K Altamura, C N Hahn, et al.
The Journal of Molecular Diagnostics : JMD
|
July 22, 2017
A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia
Ilaria S Pagani, Chung H Kok, Verity A Saunders, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 210) with videos related to
Sort By:
Page
of 21
Violence Against Women
|
March 19, 2025
Are Rape Myths Inherently Gendered? Examining Assumed Gender Ascribed to Gender-Neutral Versions of the Illinois Rape Myth Acceptance Scale Among College Students
Olivia M Kleinsmith, Olivia N Hahn, Dayna Henry, et al.
NPJ Parkinson'S Disease
|
February 29, 2024
Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson's disease phenotypes
Silke Nuber, Xiaoqun Zhang, Thomas D McCaffery, et al.
NPJ Parkinson'S Disease
|
March 13, 2024
Author Correction: Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson's disease phenotypes
Silke Nuber, Xiaoqun Zhang, Thomas D McCaffery, et al.
British Journal of Haematology
|
May 3, 2016
Apparent 'JAK2-negative' polycythaemia vera due to compound mutations in exon 14
Ing Soo Tiong, Debora A Casolari, Sarah Moore, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
August 10, 2010
Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis
King-Hwa Ling, Chelsee A Hewitt, Tim Beissbarth, et al.
Endocrine-Related Cancer
|
March 3, 2012
Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia
Lucia Gagliardi, King-Hwa Ling, Chung H Kok, et al.
Blood Advances
|
April 23, 2025
RBC Transfusion Dependency Refines the Molecular International Prognostic Scoring System for Myelodysplastic Syndrome
Thomas Wiseman, Michaela Spooner, Shreyas Khanna, et al.
BMC Medical Genetics
|
February 19, 2020
Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss
Parvathy Venugopal, Lucia Gagliardi, Cecily Forsyth, et al.
Leukemia
|
October 28, 2015
Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion gene
D M Ross, H K Altamura, C N Hahn, et al.
The Journal of Molecular Diagnostics : JMD
|
July 22, 2017
A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia
Ilaria S Pagani, Chung H Kok, Verity A Saunders, et al.
Page
of 21