Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice. - Wikidata - awgldk - TriplyDB

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

http://www.wikidata.org/entity/Q30497988

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Notch Signaling in Neuroendocrine Tumors Targeting Notch to overcome radiation resistance Anti-angiogenic alternatives to VEGF blockade Notch: a key regulator of tumor angiogenesis and metastasis Targeting γ-secretase in breast cancer A systems biology view of blood vessel growth and remodelling From fly wings to targeted cancer therapies: a centennial for notch signaling The extracellular domain of Notch2 increases its cell-surface abundance and ligand responsiveness during kidney development Endothelial cell heterogeneity In vivo visualization of Notch1 proteolysis reveals the heterogeneity of Notch1 signaling activity in the mouse cochlea.Thyroid Hormone-Induced Activation of Notch Signaling is Required for Adult Intestinal Stem Cell Development During Xenopus Laevis Metamorphosis.Notch: architect, landscaper, and guardian of the intestine.Notch signaling is required for the formation of mesangial cells from a stromal mesenchyme precursor during kidney development.Hajdu-Cheney syndrome: a review.Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry.Loss of Notch1 disrupts the barrier repair in the corneal epithelium.Control of microRNA biogenesis and transcription by cell signaling pathways.A critical role for TCF-1 in T-lineage specification and differentiation.Second-generation Notch1 activity-trap mouse line (N1IP::CreHI) provides a more comprehensive map of cells experiencing Notch1 activity Notch1 regulates the effects of matrix metalloproteinase-9 on colitis-associated cancer in mice.Notch suppresses angiogenesis and progression of hepatic metastases Investigational Notch and Hedgehog inhibitors--therapies for cardiovascular disease.Notch signaling in Sertoli cells regulates cyclical gene expression of Hes1 but is dispensable for mouse spermatogenesis.Notch signaling in ocular vasculature development and diseases.EGFL7: a unique angiogenic signaling factor in vascular development and disease Notch signaling in skeletal health and disease.The intracellular domains of Notch1 and Notch2 are functionally equivalent during development and carcinogenesis Tissue Specific Expression of Cre in Rat Tyrosine Hydroxylase and Dopamine Active Transporter-Positive Neurons.The double-edged sword of Notch signaling in cancer.Overview of genetic tools and techniques to study Notch signaling in mice.Notch signaling in developmental and tumor angiogenesis.Inhibition of delta-like ligand 4 induces luteal hypervascularization followed by functional and structural luteolysis in the primate ovary.Notch signal strength controls cell fate in the haemogenic endothelium Blockade of individual Notch ligands and receptors controls graft-versus-host disease Illuminating cancer systems with genetically engineered mouse models and coupled luciferase reporters in vivo Notch Signaling and the Skeleton.Complementary genomic screens identify SERCA as a therapeutic target in NOTCH1 mutated cancer.zebraflash transgenic lines for in vivo bioluminescence imaging of stem cells and regeneration in adult zebrafish.Notch1 and 4 signaling responds to an increasing vascular wall shear stress in a rat model of arteriovenous malformations.Cancer stem cells in lung cancer: Evidence and controversies.

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P2860

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

http://www.wikidata.org/entity/Q30497988

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

@ast

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

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type

label

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

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Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

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prefLabel

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

@ast

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.

@en

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Journal of Clinical Investigation

P1476

Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice

@en

P2093

Ahu Turkoz

http://www.w3.org/2001/XMLSchema#string

David R Piwnica-Worms

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Erin N Jackson

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Joel R Garbow

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John A Engelbach

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Zhenyi Liu

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P2860

Direct inhibition of the NOTCH transcription factor complex

Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

Notch-deficient skin induces a lethal systemic B-lymphoproliferative disorder by secreting TSLP, a sentinel for epidermal integrity

Therapeutic antibody targeting of individual Notch receptors

Generalized lacZ expression with the ROSA26 Cre reporter strain

Notch1 is required for the coordinate segmentation of somites

The canonical Notch signaling pathway: unfolding the activation mechanism.

Notch/gamma-secretase inhibition turns proliferative cells in intestinal crypts and adenomas into goblet cells

Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia

Notch1 functions as a tumor suppressor in mouse skin

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2

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121

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Joseph C. Corbo

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2011-01-25T00:00:00Z

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21266774

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3026721

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