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Nature Medicine
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April 26, 2011
GDF-15 is an inhibitor of leukocyte integrin activation required for survival after myocardial infarction in mice
Tibor Kempf, Alexander Zarbock, Christian Widera, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 29, 2025
MuSK Regulates Neuromuscular Junction Nav1.4 Localization and Excitability
Lauren A Fish, Madison D Ewing, Kelly A Rich, et al.
Biological Psychiatry
|
April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
Susan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Plos One
|
February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genes
Ravinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Brain : a Journal of Neurology
|
February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
Laura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.
Nature Medicine
|
January 13, 2015
Myeloid-derived growth factor (C19orf10) mediates cardiac repair following myocardial infarction
Mortimer Korf-Klingebiel, Marc R Reboll, Stefanie Klede, et al.
European Journal of Human Genetics : EJHG
|
June 23, 2011
Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function
Alex R Paciorkowski, Liu Lin Thio, Jill A Rosenfeld, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 31, 2002
Preoperative therapy with trastuzumab and paclitaxel followed by sequential adjuvant doxorubicin/cyclophosphamide for HER2 overexpressing stage II or III breast cancer: a pilot study
Harold J Burstein, Lyndsay N Harris, Rebecca Gelman, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2
William B Dobyns, Ghayda Mirzaa, Susan L Christian, et al.
Page
of 48
Search research articles
Search
Showing results (441-450 of 478) with videos related to
Sort By:
Page
of 48
Nature Medicine
|
April 26, 2011
GDF-15 is an inhibitor of leukocyte integrin activation required for survival after myocardial infarction in mice
Tibor Kempf, Alexander Zarbock, Christian Widera, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 29, 2025
MuSK Regulates Neuromuscular Junction Nav1.4 Localization and Excitability
Lauren A Fish, Madison D Ewing, Kelly A Rich, et al.
Biological Psychiatry
|
April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
Susan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Plos One
|
February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genes
Ravinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Brain : a Journal of Neurology
|
February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
Laura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.
Nature Medicine
|
January 13, 2015
Myeloid-derived growth factor (C19orf10) mediates cardiac repair following myocardial infarction
Mortimer Korf-Klingebiel, Marc R Reboll, Stefanie Klede, et al.
European Journal of Human Genetics : EJHG
|
June 23, 2011
Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function
Alex R Paciorkowski, Liu Lin Thio, Jill A Rosenfeld, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 31, 2002
Preoperative therapy with trastuzumab and paclitaxel followed by sequential adjuvant doxorubicin/cyclophosphamide for HER2 overexpressing stage II or III breast cancer: a pilot study
Harold J Burstein, Lyndsay N Harris, Rebecca Gelman, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2
William B Dobyns, Ghayda Mirzaa, Susan L Christian, et al.
Page
of 48