A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesis (Q28511015)

Choline kinase alpha

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Choline kinase beta

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Creatine kinase, muscle

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Dystrophin, muscular dystrophy

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Roger B. Sher

1

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25 January 2017

Chieko Aoyama

2

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25 January 2017

Kimberly A. Huebsch

3

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25 January 2017

Shaonin Ji

4

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25 January 2017

Janos Kerner

5

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25 January 2017

Yan Yang

6

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25 January 2017

Wayne N. Frankel

7

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25 January 2017

Charles L. Hoppel

8

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25 January 2017

Philip A. Wood

9

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25 January 2017

Dennis E. Vance

10

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25 January 2017

Gregory A. Cox

Journal of Biological Chemistry

11

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25 January 2017

language of work or name

English

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publication date

24 February 2006

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25 January 2017

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25 January 2017

281

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25 January 2017

8

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25 January 2017

4938–4948

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25 January 2017

Dystrophin and muscular dystrophy: past, present, and future

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Muscular dystrophy into the new millennium

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Molecular basis of muscular dystrophies.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Glycosylation defects: a new mechanism for muscular dystrophy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

The endomembrane requirement for cell surface repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Plasma Membrane Disruption: Repair, Prevention, Adaptation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Dysferlin and the plasma membrane repair in muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Structure and function of choline kinase isoforms in mammalian cells

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Choline/ethanolamine kinase from mammalian tissues

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Regulation of transbilayer plasma membrane phospholipid asymmetry

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Phosphatidylcholine and cell death

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Biochemical and evolutionary significance of phospholipid methylation

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Regulation of mitogenesis by water-soluble phospholipid intermediates

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Expression and characterization of the active molecular forms of choline/ethanolamine kinase-alpha and -beta in mouse tissues, including carbon tetrachloride-induced liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Molecular species of glycerophospholipids and sphingomyelins of human plasma: comparison to red blood cells

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Defining the importance of phosphatidylserine synthase 2 in mice

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Defective membrane repair in dysferlin-deficient muscular dystrophy

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Studies on giant mitochondria

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathy

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Disruption of the murine gene encoding phosphatidylethanolamine N-methyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Structural and functional genomics of the CPT1B gene for muscle-type carnitine palmitoyltransferase I in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

The gene encoding muscle-type carnitine palmitoyltransferase I: comparison of the 5'-upstream region of human and rodent genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Novel expression of equivocal messages containing both regions of choline/ethanolamine kinase and muscle type carnitine palmitoyltransferase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

New reagents for phosphatidylserine recognition and detection of apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Skeletal muscle metabolism in Duchenne muscular dystrophy (DMD): an in-vitro proton NMR spectroscopy study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Biochemical characterization of muscle tissue of limb girdle muscular dystrophy: an 1H and 13C NMR study

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Mechanisms of resistance to pathogenesis in muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Interaction of dystrophin rod domain with membrane phospholipids. Evidence of a close proximity between tryptophan residues and lipids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Transmembrane asymmetry and lateral domains in biological membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Chemical control of phospholipid distribution across bilayer membranes

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Identification of a functional role for lipid asymmetry in biological membranes: Phosphatidylserine-skeletal protein interactions modulate membrane stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Phosphatidylserine exposure and red cell viability in red cell aging and in hemolytic anemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

21 January 2018

How mitochondria fuse

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https://api.crossref.org/works/10.1074%2FJBC.M512578200

Pharmacogenetic analysis of rosiglitazone-induced hepatosteatosis in new mouse models of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

A Slight Asymmetry in the Transbilayer Distribution of Lysophosphatidylcholine Alters the Surface Properties and Poly(ethylene glycol)-Mediated Fusion of Dipalmitoylphosphatidylcholine Large Unilamellar Vesicles†

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M512578200

21 January 2018

Identifiers

DOI

10.1074/JBC.M512578200

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Consolidated OpenCitations Corpus – April 2017

1836770

1836770

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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