UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Thalamocortical Circuit Dysfunctions in Schizophrenia: Insights From 22q11.2 Deletion Syndrome

Biological psychiatry : cognitive neuroscience and neuroimaging, 2020-09, Vol.5 (9), p.842-843

Tanigaki, Kenji

2020

Volltextzugriff (PDF)

Regulation of lymphocyte development by Notch signaling

Nature Immunology, 2007-05, Vol.8 (5), p.451-456

2007

Volltextzugriff (PDF)

Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice

Molecular psychiatry, 2022-02, Vol.27 (2), p.929-938

2022

Volltextzugriff (PDF)

Inhibition of VEGF receptors induces pituitary apoplexy: An experimental study in mice

PloS one, 2023-03, Vol.18 (3), p.e0279634-e0279634

2023

Volltextzugriff (PDF)

Neuronal migration abnormalities and its possible implications for schizophrenia

Frontiers in neuroscience, 2015-03, Vol.9, p.74-74

2015

Volltextzugriff (PDF)

Cancer-wide in silico analyses using differentially expressed genes demonstrate the functions and clinical relevance of JAG, DLL, and NOTCH

PloS one, 2024-07, Vol.19 (7), p.e0307943

2024

Volltextzugriff (PDF)

An epidemiological study of season of birth, mental health, and neuroimaging in the UK Biobank

PloS one, 2024-05, Vol.19 (5), p.e0300449-e0300449

2024

Volltextzugriff (PDF)

Zmiz1 is a novel regulator of lymphatic endothelial cell gene expression and function

PloS one, 2024-05, Vol.19 (5), p.e0302926-e0302926

2024

Volltextzugriff (PDF)

Contribution of Endothelial-to-Mesenchymal Transition to the Pathogenesis of Human Cerebral and Orbital Cavernous Malformations

Neurosurgery, 2017-07, Vol.81 (1), p.176-183

2017

Volltextzugriff (PDF)

Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary study

PloS one, 2024, Vol.19 (5), p.e0303343-e0303343

2024

Volltextzugriff (PDF)

Notch signaling drives IL-22 secretion in CD4⁺ T cells by stimulating the aryl hydrocarbon receptor

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (13), p.5943-5948

2010

Volltextzugriff (PDF)

B7-H3 Suppresses Antitumor Immunity via the CCL2-CCR2-M2 Macrophage Axis and Contributes to Ovarian Cancer Progression

Cancer immunology research, 2022-01, Vol.10 (1), p.56-69

2022

Volltextzugriff (PDF)

Machine Learning for Diagnosis of AD and Prediction of MCI Progression From Brain MRI Using Brain Anatomical Analysis Using Diffeomorphic Deformation

Frontiers in neurology, 2021-02, Vol.11, p.576029-576029

2021

Volltextzugriff (PDF)

Two Opposing Roles of RBP-J in Notch Signaling

Current Topics in Developmental Biology, 2010, Vol.92, p.231-252

2010

Volltextzugriff (PDF)

Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants

Genes & development, 2004-10, Vol.18 (20), p.2469-2473

2004

Volltextzugriff (PDF)

Notch signaling regulates nucleocytoplasmic Olig2 translocation in reactive astrocytes differentiation after ischemic stroke

Neuroscience research, 2013-03, Vol.75 (3), p.204-209

2013

Volltextzugriff (PDF)

Sex-related difference in human white matter volumes studied: Inspection of the corpus callosum and other white matter by VBM

Scientific reports, 2017-01, Vol.7 (1), p.39818-39818, Article 39818

2017

Volltextzugriff (PDF)

Role of Endothelial-to-Mesenchymal Transition in the Pathogenesis of Central Nervous System Hemangioblastomas

World neurosurgery, 2018-09, Vol.117, p.e187-e193

2018

Volltextzugriff (PDF)

Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model

Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (43), p.17552-17557

2013

Volltextzugriff (PDF)

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain

Human molecular genetics, 2012-08, Vol.21 (15), p.3489-3499

2012

Volltextzugriff (PDF)

Stromal cells of hemangioblastomas exhibit mesenchymal stem cell-derived vascular progenitor cell properties

Brain tumor pathology, 2018-10, Vol.35 (4), p.193-201

2018

Volltextzugriff (PDF)

Kif14 mutation causes severe brain malformation and hypomyelination

PloS one, 2013-01, Vol.8 (1), p.e53490-e53490

2013

Volltextzugriff (PDF)

Contribution of PROP1 in the pathogenesis of Cushing’s disease: A preliminary study

Interdisciplinary neurosurgery : Advanced techniques and case management, 2023-03, Vol.31, p.101691, Article 101691

2023

Volltextzugriff (PDF)

Notch-RBP-J signaling is involved in cell fate determination of marginal zone B cells

Nature immunology, 2002-05, Vol.3 (5), p.443-450

2002

Volltextzugriff (PDF)

Preparation of Robust Metal‐Free Magnetic Nanoemulsions Encapsulating Low‐Molecular‐Weight Nitroxide Radicals and Hydrophobic Drugs Directed Toward MRI‐Visible Targeted Delivery

Chemistry : a European journal, 2017-11, Vol.23 (62), p.15713-15720

2017

Volltextzugriff (PDF)

1 – 25 von 99

Suche als RSS-Feed

Aktive Filter

KollektionTaylor & Francis Journals Auto-Holdings Collection

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(88)
Mit Volltextzugriff
(94)

Publikationsform

Sprache

Englisch
(93)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(69)
Life Sciences & Biomedicine
(48)
Animals
(39)
Mice
(33)
Humans
(20)
Mice, Knockout
(15)
Male
(14)
Neurosciences & Neurology
(14)
Female
(12)
Mice, Transgenic
(12)
Physical Sciences
(12)
Multidisciplinary Sciences
(11)
Science & Technology - Other Topics
(11)
Signal Transduction
(11)
Immunoglobulin J Recombination Signal Sequence-Binding Protein
(10)
Neurosciences
(10)
Immunology
(9)
Mice, Inbred C57bl
(8)
Receptors, Notch
(8)
Receptors, Notch - Metabolism
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Thalamocortical Circuit Dysfunctions in Schizophrenia: Insights From 22q11.2 Deletion Syndrome

Regulation of lymphocyte development by Notch signaling

Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice

Inhibition of VEGF receptors induces pituitary apoplexy: An experimental study in mice

Neuronal migration abnormalities and its possible implications for schizophrenia

Cancer-wide in silico analyses using differentially expressed genes demonstrate the functions and clinical relevance of JAG, DLL, and NOTCH

An epidemiological study of season of birth, mental health, and neuroimaging in the UK Biobank

Zmiz1 is a novel regulator of lymphatic endothelial cell gene expression and function

Contribution of Endothelial-to-Mesenchymal Transition to the Pathogenesis of Human Cerebral and Orbital Cavernous Malformations

Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary study

Notch signaling drives IL-22 secretion in CD4⁺ T cells by stimulating the aryl hydrocarbon receptor

B7-H3 Suppresses Antitumor Immunity via the CCL2-CCR2-M2 Macrophage Axis and Contributes to Ovarian Cancer Progression

Machine Learning for Diagnosis of AD and Prediction of MCI Progression From Brain MRI Using Brain Anatomical Analysis Using Diffeomorphic Deformation

Two Opposing Roles of RBP-J in Notch Signaling

Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants

Notch signaling regulates nucleocytoplasmic Olig2 translocation in reactive astrocytes differentiation after ischemic stroke

Sex-related difference in human white matter volumes studied: Inspection of the corpus callosum and other white matter by VBM

Role of Endothelial-to-Mesenchymal Transition in the Pathogenesis of Central Nervous System Hemangioblastomas

Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain

Stromal cells of hemangioblastomas exhibit mesenchymal stem cell-derived vascular progenitor cell properties

Kif14 mutation causes severe brain malformation and hypomyelination

Contribution of PROP1 in the pathogenesis of Cushing’s disease: A preliminary study

Notch-RBP-J signaling is involved in cell fate determination of marginal zone B cells

Preparation of Robust Metal‐Free Magnetic Nanoemulsions Encapsulating Low‐Molecular‐Weight Nitroxide Radicals and Hydrophobic Drugs Directed Toward MRI‐Visible Targeted Delivery

Aktive Filter

Suchergebnisse filtern