A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
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Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesisThe Exocyst Complex in Health and DiseaseNotch-deficient skin induces a lethal systemic B-lymphoproliferative disorder by secreting TSLP, a sentinel for epidermal integrityAbcb10 physically interacts with mitoferrin-1 (Slc25a37) to enhance its stability and function in the erythroid mitochondriaA novel murine protein with no effect on iron homoeostasis is homologous with transferrin and is the putative inhibitor of carbonic anhydraseSnx3 regulates recycling of the transferrin receptor and iron assimilationIron and porphyrin trafficking in heme biogenesis.Mitochondrial iron trafficking and the integration of iron metabolism between the mitochondrion and cytosol.Gene co-expression networks shed light into diseases of brain iron accumulation.Normal and disordered reticulocyte maturation.The long history of iron in the Universe and in health and disease.Cellular and mitochondrial iron homeostasis in vertebratesDynamic control of hepatic Plasmodium numbers by hepcidin despite elevated liver iron during iron supplementationDisruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant.A functional interplay between the small GTPase Rab11a and mitochondria-shaping proteins regulates mitochondrial positioning and polarization of the actin cytoskeleton downstream of Src family kinases.Brain iron homeostasis: from molecular mechanisms to clinical significance and therapeutic opportunitiesMolecular basis of hereditary iron homeostasis defects.The emerging role of iron dyshomeostasis in the mitochondrial decay of aging.Iron and erythropoiesis: a dual relationship.How I manage patients with atypical microcytic anaemia.Regulation of heme biosynthesis and transport in metazoa.Diverse Functions and Signal Transduction of the Exocyst Complex in Tumor Cells.A Red Carpet for Iron Metabolism.A potential link between insulin signaling and GLUT4 translocation: Association of Rab10-GTP with the exocyst subunit Exoc6/6b.Exocyst function is regulated by effector phosphorylation.Characterization of Putative Erythroid Regulators of Hepcidin in Mouse Models of Anemia.Rab11 supports amphetamine-stimulated norepinephrine transporter trafficking.Intracellular iron and heme trafficking and metabolism in developing erythroblasts.Loss of Dynamin 2 GTPase function results in microcytic anaemia.An exocyst complex functions in plant cell growth in Arabidopsis and tobacco.
P2860
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P2860
A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
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2005年学术文章
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2005年学术文章
@zh-hans
2005年学术文章
@zh-my
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2005年學術文章
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2005年學術文章
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name
A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
@en
A mutation in Sec15l1 causes anemia in hemoglobin deficit
@nl
type
label
A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
@en
A mutation in Sec15l1 causes anemia in hemoglobin deficit
@nl
prefLabel
A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
@en
A mutation in Sec15l1 causes anemia in hemoglobin deficit
@nl
P2093
P2860
P50
P356
P1433
P1476
A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice.
@en
P2093
Cameron C Trenor
Carolyn Bennett
Jackie E Lim
Kelly Morgan
P2860
P2888
P304
P356
10.1038/NG1659
P407
P577
2005-10-16T00:00:00Z