Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis. - Wikidata - wikimedia - TriplyDB

Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.

Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.

http://www.wikidata.org/entity/Q42742627

about

Musculoskeletal Manifestations of Sickle Cell Disease: A Review The Biology of Annexin A2: From Vascular Fibrinolysis to Innate Immunity Genomic approaches to identifying targets for treating β hemoglobinopathies Sickle cell disease: a multigenic perspective of a single gene disorder.Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study Bone morphogenetic protein 6 polymorphisms are associated with radiographic progression in ankylosing spondylitis.High-density SNP genotyping to define beta-globin locus haplotypes.Erythrocytapheresis: Do Not Forget a Useful Therapy!Klotho: its various functions and association with sickle cell disease subphenotypes.Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.Avascular necrosis in pediatric systemic lupus erythematosus: a brief report and review of the literature.Microarchitectural and mechanical characterization of the sickle bone.Genetic modifiers of sickle cell disease The annexin A2/S100A10 system in health and disease: emerging paradigms Klotho locus, metabolic traits, and serum hemoglobin in hospitalized older patients: a genetic association analysis.Bone vascularization in normal and disease conditions.Annexin A2 system in human biology: cell surface and beyond.Genome-wide association studies and the genetic dissection of complex traits.Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.The search for genetic modifiers of disease severity in the β-hemoglobinopathies.Differential label-free quantitative proteomic analysis of avian eggshell matrix and uterine fluid proteins associated with eggshell mechanical property.Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.Intravascular hemolysis and the pathophysiology of sickle cell disease.Osteonecrosis in genetic disorders.Klotho gene polymorphisms and their association with sickle cell disease phenotypes.Histological and elemental analyses of impaired bone mineralization in klotho-deficient mice.

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P2860

Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.

http://www.wikidata.org/entity/Q42742627

description

2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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2005年论文

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2005年论文

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name

Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

@en

Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

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type

label

Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

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Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

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prefLabel

Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

@en

Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

@nl

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BLOOD-2005-02-0548

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Association of klotho, bone mo ...... ith sickle cell osteonecrosis.

@en

P2093

Alice Bisbee

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Diego F Wyszynski

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John Farrell

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Qian-Li Ma

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Stephen H Embury

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Vikki G Nolan

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P2860

SB-431542 is a potent and specific inhibitor of transforming growth factor-beta superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7

Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia

A New Statistical Method for Haplotype Reconstruction from Population Data

Haploview: analysis and visualization of LD and haplotype maps

Inhibition of transforming growth factor (TGF)-beta1-induced extracellular matrix with a novel inhibitor of the TGF-beta type I receptor kinase activity: SB-431542

Klotho, a gene related to a syndrome resembling human premature aging, functions in a negative regulatory circuit of vitamin D endocrine system

cDNA microarray analysis of changes in gene expression induced by neuronal hypoxia in vitro

Activation of bone morphogenetic protein/Smad signaling in bronchial epithelial cells during airway inflammation

A comparison of bayesian methods for haplotype reconstruction from population genotype data.

Ectopic osteogenesis using adenoviral bone morphogenetic protein (BMP)-4 and BMP-6 gene transfer.

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10.1182/BLOOD-2005-02-0548

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1

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Clinton Baldwin

Martin H Steinberg

Lindsay A. Farrer

Paola Sebastiani

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7949944

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sickle-cell disease

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