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Kelch proteins: emerging roles in skeletal muscle development and diseases.
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PubMed
title
Kelch proteins: emerging roles in skeletal muscle development and diseases.
(English)
1 reference
stated in
PubMed
author
Alan H. Beggs
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
author name string
Vandana A Gupta
series ordinal
1
2 references
stated in
Crossref
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
publication date
1 June 2014
1 reference
stated in
PubMed
published in
Skeletal Muscle
2 references
stated in
Crossref
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
volume
4
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
page(s)
11
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
exact match
https://scigraph.springernature.com/pub.10.1186/2044-5040-4-11
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Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
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Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan
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Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4
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Structural Basis for Cul3 Protein Assembly with the BTB-Kelch Family of E3 Ubiquitin Ligases
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Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa
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BTB Protein KLHL12 targets the dopamine D4 receptor for ubiquitination by a Cul3-based E3 ligase
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A Cul3-based E3 ligase removes Aurora B from mitotic chromosomes, regulating mitotic progression and completion of cytokinesis in human cells
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Role of phosphorylation on the structural dynamics and function of types III and IV intermediate filaments
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Ubiquitination of Keap1, a BTB-Kelch substrate adaptor protein for Cul3, targets Keap1 for degradation by a proteasome-independent pathway
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BTB protein Keap1 targets antioxidant transcription factor Nrf2 for ubiquitination by the Cullin 3-Roc1 ligase
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Novel kelch-like protein, KLEIP, is involved in actin assembly at cell-cell contact sites of Madin-Darby canine kidney cells
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The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)
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Cullin-3 targets cyclin E for ubiquitination and controls S phase in mammalian cells
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Muskelin, a novel intracellular mediator of cell adhesive and cytoskeletal responses to thrombospondin-1
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RING domain E3 ubiquitin ligases
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Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity
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Identification of Kel1p, a kelch domain-containing protein involved in cell fusion and morphology in Saccharomyces cerevisiae
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The Keap1 BTB/POZ dimerization function is required to sequester Nrf2 in cytoplasm
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A human homologue of Drosophila kelch associates with myosin-VIIa in specialized adhesion junctions
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Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis
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Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
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The kelch repeat superfamily of proteins: propellers of cell function
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Emerging roles of Nrf2 and phase II antioxidant enzymes in neuroprotection
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Congenital muscular dystrophies: a brief review
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Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization
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A novel mutation in two families with limb-girdle muscular dystrophy type 2C
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The ubiquitin-proteasome system
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Kbtbd5 is regulated by MyoD and restricted to the myogenic lineage
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20 March 2017
BTB-Kelch protein Krp1 regulates proliferation and differentiation of myoblasts
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20 March 2017
Krp1 (Sarcosin) promotes lateral fusion of myofibril assembly intermediates in cultured mouse cardiomyocytes
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Targeted deletion of a single Sca8 ataxia locus allele in mice causes abnormal gait, progressive loss of motor coordination, and Purkinje cell dendritic deficits
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Haploinsufficiency of kelch-like protein homolog 10 causes infertility in male mice
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20 March 2017
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
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20 March 2017
Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments
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Interaction of an intracellular pentraxin with a BTB-Kelch protein is associated with ubiquitylation, aggregation and neuronal apoptosis
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20 March 2017
The BTB-kelch protein KLHL6 is involved in B-lymphocyte antigen receptor signaling and germinal center formation
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Protective role of Nd1 in doxorubicin-induced cardiotoxicity
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20 March 2017
Krp1, a novel kelch related protein that is involved in pseudopod elongation in transformed cells
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
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Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation
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Ubiquitin system: direct effects join the signaling
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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29 September 2017
The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy
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29 September 2017
The novel BTB-kelch protein, KBTBD8, is located in the Golgi apparatus and translocates to the spindle apparatus during mitosis
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Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.
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Keap1 knockdown increases markers of metabolic syndrome after long-term high fat diet feeding
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A Cul-3-BTB ubiquitylation pathway regulates junctional levels and asymmetry of core planar polarity proteins
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29 September 2017
Mechanisms for maintaining muscle
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29 September 2017
The Kelch repeat protein KLHDC10 regulates oxidative stress-induced ASK1 activation by suppressing PP5.
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29 September 2017
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
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29 September 2017
Regulation and physiological roles of the calpain system in muscular disorders
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29 September 2017
KBTBD13 interacts with Cullin 3 to form a functional ubiquitin ligase
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29 September 2017
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores
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29 September 2017
Building muscle: molecular regulation of myogenesis.
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29 September 2017
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
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29 September 2017
Distal myopathies--new genetic entities expand diagnostic challenge
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Nemaline myopathies.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
The cullin protein family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Sensory-motor deficits and neurofilament disorganization in gigaxonin-null mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
KEAP1 gene mutations and NRF2 activation are common in pulmonary papillary adenocarcinoma
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Many routes to the same destination: lessons from skeletal muscle development.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Muscular dystrophies: an update on pathology and diagnosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Autophagy in skeletal muscle
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Drosophila Kelch functions with Cullin-3 to organize the ring canal actin cytoskeleton
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
A kelch family protein Nd1-L functions as a metastasis suppressor in cancer cells via Rho family proteins mediated mechanism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Diversification of the cullin family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Klhl31 is associated with skeletal myogenesis and its expression is regulated by myogenic signals and Myf-5.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
NAC1, a POZ/BTB protein that functions as a corepressor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Pathological defects in congenital myopathies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
The involvement of the ubiquitin proteasome system in human skeletal muscle remodelling and atrophy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Molecular control of mammalian myoblast fusion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
A novel human BTB-kelch protein KLHL31, strongly expressed in muscle and heart, inhibits transcriptional activities of TRE and SRE.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Novel role of the muskelin-RanBP9 complex as a nucleocytoplasmic mediator of cell morphology regulation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Myofibrillar protein turnover: the proteasome and the calpains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Neuronal expression of muskelin in the rodent central nervous system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
The BTB-Kelch protein KLEIP controls endothelial migration and sprouting angiogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Born to bind: the BTB protein-protein interaction domain.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Into the heart: the emerging role of the ubiquitin-proteasome system.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Detection of autoantibodies to the BTB-kelch protein KLHL7 in cancer sera
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
The ubiquitin-proteasome system and skeletal muscle wasting
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
The BACK domain in BTB-kelch proteins.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Genetic alterations of the NRP/B gene are associated with human brain tumors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Apoptosis in heart and skeletal muscle.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Identification of Nd1, a novel murine kelch family protein, involved in stabilization of actin filaments
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Apoptosis and muscle fibre loss in neuromuscular disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Excitability is mediated by the T1 domain of the voltage-gated potassium channel.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
All in the family: the BTB/POZ, KRAB, and SCAN domains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
Fold prediction and evolutionary analysis of the POZ domain: structural and evolutionary relationship with the potassium channel tetramerization domain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
29 September 2017
CUL3 and protein kinases: insights from PLK1/KLHL22 interaction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
2 June 2018
Disruption of Nrf2/ARE signaling impairs antioxidant mechanisms and promotes cell degradation pathways in aged skeletal muscle
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
2 June 2018
Calpainopathy-a survey of mutations and polymorphisms
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
2 June 2018
Overexpression of Nd1, a novel Kelch family protein, in the heart of transgenic mice protects against doxorubicin-induced cardiomyopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1186%2F2044-5040-4-11
retrieved
21 January 2018
Pallial expression of Enc1 RNA in postnatal mouse telencephalon.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1186%2F2044-5040-4-11
retrieved
21 January 2018
Targeting of protein ubiquitination by BTB–Cullin 3–Roc1 ubiquitin ligases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1186%2F2044-5040-4-11
retrieved
21 January 2018
Gene targeting of GAN in mouse causes a toxic accumulation of microtubule-associated protein 8 and impaired retrograde axonal transport.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1186%2F2044-5040-4-11
retrieved
21 January 2018
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1186%2F2044-5040-4-11
retrieved
21 January 2018
SCA8 mRNA expression suggests an antisense regulation of KLHL1 and correlates to SCA8 pathology.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
27 November 2018
ribbon encodes a novel BTB/POZ protein required for directed cell migration in Drosophila melanogaster
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
27 November 2018
The BTB/POZ domain: a new protein-protein interaction motif common to DNA- and actin-binding proteins.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4067060
retrieved
27 November 2018
Differential subcellular localization and activity of kelch repeat proteins KLHDC1 and KLHDC2
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Overexpression of Kelch domain containing-2 (mKlhdc2) inhibits differentiation and directed migration of C2C12 myoblasts
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Muscular dystrophies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
[Mutation of KLHL-10 in idiopathic infertile males with azoospermia, oligospermia or asthenospermia]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Roles of Keap1-Nrf2 system in upper aerodigestive tract carcinogenesis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
BTB/POZ domain proteins are putative substrate adaptors for cullin 3 ubiquitin ligases
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24959344
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1186/2044-5040-4-11
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3179097
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
Dimensions Publication ID
1041045662
0 references
OpenCitations bibliographic resource ID
3179097
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3179097
PMCID
4067060
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3179097
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
PubMed ID
24959344
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3179097
stated in
Europe PubMed Central
PMCID
4067060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24959344%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 June 2020
ResearchGate publication ID
263432589
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