Search research articles
Contact Us
Filters
Showing results (271-280 of 281) with videos related to
Page
of 29
Sort By:
Nature Communications
|
October 20, 2019
Sialic acid mediated mechanical activation of β<sub>2</sub> adrenergic receptors by bacterial pili
Zoe Virion, Stéphane Doly, Kusumika Saha, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1996
The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis
R Quinton, V M Duke, P A de Zoysa, et al.
Leukemia
|
April 22, 2006
The sesquiterpene lactone parthenolide induces selective apoptosis of B-chronic lymphocytic leukemia cells in vitro
A J Steele, D T Jones, K Ganeshaguru, et al.
Clinical Endocrinology
|
September 5, 2001
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization
R Quinton, V M Duke, A Robertson, et al.
Biomedicines
|
July 2, 2020
Identification of Differentially Methylated CpG Sites in Fibroblasts from Keloid Scars
Mansour A Alghamdi, Hilary J Wallace, Phillip E Melton, et al.
Blood
|
August 7, 2008
p53-mediated apoptosis of CLL cells: evidence for a transcription-independent mechanism
Andrew J Steele, Archibald G Prentice, A Victor Hoffbrand, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
Two amyloid precursor protein transgenic mouse models with Alzheimer disease-like pathology
C Sturchler-Pierrat, D Abramowski, M Duke, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine
|
September 15, 2022
Development of strategies for community engaged research dissemination by basic scientists: a case study
Elizabeth C Stewart, Jamaine S Davis, Treniqka S Walters, et al.
Human Molecular Genetics
|
April 6, 2000
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
D W Morris, L Robinson, D Turic, et al.
Molecular Psychiatry
|
March 1, 2003
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22
D Turic, L Robinson, M Duke, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 281) with videos related to
Sort By:
Page
of 29
Nature Communications
|
October 20, 2019
Sialic acid mediated mechanical activation of β<sub>2</sub> adrenergic receptors by bacterial pili
Zoe Virion, Stéphane Doly, Kusumika Saha, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1996
The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis
R Quinton, V M Duke, P A de Zoysa, et al.
Leukemia
|
April 22, 2006
The sesquiterpene lactone parthenolide induces selective apoptosis of B-chronic lymphocytic leukemia cells in vitro
A J Steele, D T Jones, K Ganeshaguru, et al.
Clinical Endocrinology
|
September 5, 2001
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization
R Quinton, V M Duke, A Robertson, et al.
Biomedicines
|
July 2, 2020
Identification of Differentially Methylated CpG Sites in Fibroblasts from Keloid Scars
Mansour A Alghamdi, Hilary J Wallace, Phillip E Melton, et al.
Blood
|
August 7, 2008
p53-mediated apoptosis of CLL cells: evidence for a transcription-independent mechanism
Andrew J Steele, Archibald G Prentice, A Victor Hoffbrand, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
Two amyloid precursor protein transgenic mouse models with Alzheimer disease-like pathology
C Sturchler-Pierrat, D Abramowski, M Duke, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine
|
September 15, 2022
Development of strategies for community engaged research dissemination by basic scientists: a case study
Elizabeth C Stewart, Jamaine S Davis, Treniqka S Walters, et al.
Human Molecular Genetics
|
April 6, 2000
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
D W Morris, L Robinson, D Turic, et al.
Molecular Psychiatry
|
March 1, 2003
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22
D Turic, L Robinson, M Duke, et al.
Page
of 29