Actinin-associated LIM protein-deficient mice maintain normal development and structure of skeletal muscle (Q28585840)

31 January 2017

title

Actinin-associated LIM protein-deficient mice maintain normal development and structure of skeletal muscle (English)

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31 January 2017

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GOA release 2020-03-11

author name string

K. Jo

1

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31 January 2017

B. Rutten

2

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31 January 2017

R. C. Bunn

3

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31 January 2017

D. S. Bredt

4

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31 January 2017

language of work or name

English

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publication date

1 March 2001

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Molecular and Cellular Biology

31 January 2017

published in

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31 January 2017

volume

21

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31 January 2017

issue

5

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31 January 2017

page(s)

1682–1687

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Purification and characterization of an alpha-actinin-binding PDZ-LIM protein that is up-regulated during muscle differentiation

31 January 2017

cites work

1 reference

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Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C

17 March 2017

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Characterization of MALS/Velis-1, -2, and -3: a family of mammalian LIN-7 homologs enriched at brain synapses in association with the postsynaptic density-95/NMDA receptor postsynaptic complex

17 March 2017

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

17 March 2017

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Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifs

17 March 2017

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Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

17 March 2017

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Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains

17 March 2017

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Muscle LIM protein, a novel essential regulator of myogenesis, promotes myogenic differentiation

17 March 2017

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Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

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Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene

17 March 2017

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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

17 March 2017

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24 May 2017

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Oracle, a novel PDZ-LIM domain protein expressed in heart and skeletal muscle

29 September 2017

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Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes

29 September 2017

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29 September 2017

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

29 September 2017

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PDZs and receptor/channel clustering: rounding up the latest suspects

29 September 2017

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Novel gene transcripts preferentially expressed in human muscles revealed by quantitative hybridization of a high density cDNA array

29 September 2017

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The enigma of LIM domains

29 September 2017

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

29 September 2017

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The LIM domain: a new structural motif found in zinc-finger-like proteins.

29 September 2017

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The LIM domain is a modular protein-binding interface

29 September 2017

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29 September 2017

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Overexcited or inactive: ion channels in muscle disease

29 September 2017

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Interaction of ion channels and receptors with PDZ domain proteins

29 September 2017

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Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

3 June 2018

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PDZ proteins organize synaptic signaling pathways

20 June 2018

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Two genetically separable steps in the differentiation of thymic epithelium.

27 November 2018

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Specific spectrophotometric assay for the M isoenzymes of pyruvate kinase in plasma samples containing mixtures of the muscle (M) and liver (L) isoenzymes

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/11238905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Time course of changes in plasma membrane permeability in the dystrophin-deficient mdx mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/11238905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11238905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1128/MCB.21.5.1682-1687.2001

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