about
c-Jun regulates cell cycle progression and apoptosis by distinct mechanismsLoss of skeletal muscle HIF-1alpha results in altered exercise enduranceHIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progressionLoss of PTEN facilitates HIF-1-mediated gene expressionHypoxia-inducible factor-dependent degeneration, failure, and malignant transformation of the heart in the absence of the von Hippel-Lindau proteinLoss of Cul1 results in early embryonic lethality and dysregulation of cyclin ECited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesisUnstable kinetochore-microtubule capture and chromosomal instability following deletion of CENP-Ec-Jun is essential for organization of the epidermal leading edgeHIF-1 alpha is required for solid tumor formation and embryonic vascularization.pVHL function is essential for endothelial extracellular matrix deposition.VEGFA is necessary for chondrocyte survival during bone developmentInactivation of the arylhydrocarbon receptor nuclear translocator (Arnt) suppresses von Hippel-Lindau disease-associated vascular tumors in mice.RAG-1-deficient mice have no mature B and T lymphocytesHIF1alpha is a critical regulator of secretory differentiation and activation, but not vascular expansion, in the mouse mammary glandHypoxia-inducible factor-2 (HIF-2) regulates hepatic erythropoietin in vivoAstrocyte-derived vascular endothelial growth factor stabilizes vessels in the developing retinal vasculatureThe HIF-1/glial TIM-3 axis controls inflammation-associated brain damage under hypoxiaTranscription factor HIF-1 is a necessary mediator of the pasteur effect in mammalian cells.Cutaneous control of blood pressure.Loss of myeloid cell-derived vascular endothelial growth factor accelerates fibrosisModelling pulmonary microthrombosis coupled to metastasis: distinct effects of thrombogenesis on tumorigenesisMetabolic basis to Sherpa altitude adaptationLoss of fibroblast HIF-1α accelerates tumorigenesis.Hypoxia-inducible factors 1 and 2 are important transcriptional effectors in primary macrophages experiencing hypoxia.The asparaginyl hydroxylase factor inhibiting HIF-1alpha is an essential regulator of metabolismIncreased adipocyte O2 consumption triggers HIF-1α, causing inflammation and insulin resistance in obesity.Hypoxia-inducible factor-1α induces ErbB4 signaling in the differentiating mammary glandAngiogenesis: the role of the microenvironment in flipping the switch.Hypoxia inducible factor 1 alpha regulates T cell receptor signal transduction.Hypoxia-inducible factor-1 is a determinant of lobular structure and oxygen consumption in the liver.Dietary nitrate increases arginine availability and protects mitochondrial complex I and energetics in the hypoxic rat heart.A novel role for the hypoxia inducible transcription factor HIF-1alpha: critical regulation of inflammatory cell function.O2 regulates stem cells through Wnt/β-catenin signalling.HIF transcription factors, inflammation, and immunity.Suppression of erythropoiesis by dietary nitrate.Astrocyte pVHL and HIF-α isoforms are required for embryonic-to-adult vascular transition in the eyeHIF-1 and hypoxic response: the plot thickens.The hypoxia-inducible factor alpha pathway couples angiogenesis to osteogenesis during skeletal development.Regulation of iron homeostasis by the hypoxia-inducible transcription factors (HIFs).
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Randall S Johnson
@es
Randall S. Johnson
@en
Randall S. Johnson
@nl
Randall S. Johnson
@sl
type
label
Randall S Johnson
@es
Randall S. Johnson
@en
Randall S. Johnson
@nl
Randall S. Johnson
@sl
prefLabel
Randall S Johnson
@es
Randall S. Johnson
@en
Randall S. Johnson
@nl
Randall S. Johnson
@sl
P106
P1153
26643428400
P21
P31
P3835
randall-johnson3
P496
0000-0002-4084-6639
P569
2000-01-01T00:00:00Z