(Q38376932)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

review article

1 reference

title

Axon guidance proteins in neurological disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

author

Eljo Yvette van Battum

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Jeroen Pasterkamp

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

author name string

Sara Brignani

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

publication date

11 March 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

page(s)

532-546

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

Mechanisms and molecules of neuronal wiring: a primer

2 March 2020

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7 January 2021

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7 January 2021

Midline axon guidance and human genetic disorders

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7 January 2021

Human disorders of axon guidance

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7 January 2021

Autism spectrum disorders: developmental disconnection syndromes

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7 January 2021

Neuroanatomy of autism

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7 January 2021

Evidence for dysregulation of axonal growth and guidance in the etiology of ASD.

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7 January 2021

Axon guidance and synaptic maintenance: preclinical markers for neurodegenerative disease and therapeutics

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7 January 2021

Axon guidance proteins: novel therapeutic targets for ALS?

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7 January 2021

Repulsive guidance molecule-a and demyelination: implications for multiple sclerosis

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7 January 2021

Immunological functions of the neuropilins and plexins as receptors for semaphorins

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7 January 2021

Getting neural circuits into shape with semaphorins

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7 January 2021

Netrins: versatile extracellular cues with diverse functions

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7 January 2021

Moving away from the midline: new developments for Slit and Robo

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7 January 2021

Molecular biology, genetics and biochemistry of the repulsive guidance molecule family

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7 January 2021

Eph/ephrin signalling during development

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7 January 2021

Sonic hedgehog and Wnt: antagonists in morphogenesis but collaborators in axon guidance.

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7 January 2021

The Hedgehog, TGF-beta/BMP and Wnt families of morphogens in axon guidance.

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7 January 2021

Expression of the Wnt signaling system in central nervous system axon guidance and regeneration

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7 January 2021

Semaphorin signalling during development

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7 January 2021

Further tales of the midline.

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7 January 2021

Axonal commissures in the central nervous system: how to cross the midline?

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7 January 2021

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes

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7 January 2021

Human genetic disorders of axon guidance

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7 January 2021

Mutations in DCC cause congenital mirror movements.

1 reference

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7 January 2021

A novel DCC mutation and genetic heterogeneity in congenital mirror movements.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis

1 reference

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7 January 2021

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

1 reference

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7 January 2021

Human ROBO1 regulates interaural interaction in auditory pathways.

1 reference

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7 January 2021

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Association of the ROBO1 gene with reading disabilities in a family-based analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China

1 reference

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7 January 2021

Mutational spectrum of semaphorin 3A and semaphorin 3D genes in Spanish Hirschsprung patients

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7 January 2021

Association of the neuropilin-2 (NRP2) gene polymorphisms with autism in Chinese Han population.

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7 January 2021

Genetic analyses of roundabout (ROBO) axon guidance receptors in autism.

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7 January 2021

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

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7 January 2021

Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism

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7 January 2021

Constitutional downregulation of SEMA5A expression in autism

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7 January 2021

Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding

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7 January 2021

Transient downregulation of Sema3A mRNA in a rat model for temporal lobe epilepsy. A novel molecular event potentially contributing to mossy fiber sprouting.

1 reference

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7 January 2021

EphA/ephrin-A interactions regulate epileptogenesis and activity-dependent axonal sprouting in adult rats.

1 reference

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7 January 2021

Increased EphA/ephrinA expression in hippocampus of pilocarpine treated mouse.

1 reference

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7 January 2021

Temporal specific patterns of semaphorin gene expression in rat brain after kainic acid-induced status epilepticus.

1 reference

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7 January 2021

Abnormal expression and spatiotemporal change of Slit2 in neurons and astrocytes in temporal lobe epileptic foci: A study of epileptic patients and experimental animals

1 reference

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7 January 2021

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

The expression of the chemorepellent Semaphorin 3A is selectively induced in terminal Schwann cells of a subset of neuromuscular synapses that display limited anatomical plasticity and enhanced vulnerability in motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

High-resolution whole-genome association study of Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Analysis of gene expression in Parkinson's disease: possible involvement of neurotrophic support and axon guidance in dopaminergic cell death

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Early changes in hippocampal Eph receptors precede the onset of memory decline in mouse models of Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

EphA4 activation of c-Abl mediates synaptic loss and LTP blockade caused by amyloid-β oligomers

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Netrin-1 interacts with amyloid precursor protein and regulates amyloid-beta production

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Reversing EphB2 depletion rescues cognitive functions in Alzheimer model

1 reference

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7 January 2021

A role for semaphorin 3A signaling in the degeneration of hippocampal neurons during Alzheimer's disease

1 reference

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7 January 2021

The beta-amyloid protein of Alzheimer's disease increases neuronal CRMP-2 phosphorylation by a Rho-GTP mechanism

1 reference

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7 January 2021

A preliminary study of the whole-genome expression profile of sporadic and monogenic early-onset Alzheimer's disease

1 reference

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7 January 2021

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

1 reference

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7 January 2021

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

A novel DCC mutation and genetic heterogeneity in congenital mirror movements

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Genetic dissection of the function of hindbrain axonal commissures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Genetics of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Guiding neuronal cell migrations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Clinical genetics of Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: implications for the aetiology of hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Semaphorins in the development, homeostasis and disease of hormone systems.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Dysregulation of Semaphorin7A/β1-integrin signaling leads to defective GnRH-1 cell migration, abnormal gonadal development and altered fertility

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Semaphorin 4D regulates gonadotropin hormone-releasing hormone-1 neuronal migration through PlexinB1-Met complex

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Slit2 and Robo3 modulate the migration of GnRH-secreting neurons

1 reference

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7 January 2021

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

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7 January 2021

Hirschsprung's disease prevalence in Europe: a register based study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Semaphorin 3A expression in the colon of Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Effects of different regions of the developing gut on the migration of enteric neural crest-derived cells: A role for Sema3A, but not Sema3F

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

The genetic landscapes of autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Mossy fiber sprouting as a potential therapeutic target for epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Granule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy

1 reference

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7 January 2021

Review: neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy

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7 January 2021

Selective neuronal vulnerability in neurodegenerative diseases: from stressor thresholds to degeneration

1 reference

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7 January 2021

Synapse development and plasticity: roles of ephrin/Eph receptor signaling

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7 January 2021

Semaphorin function in neural plasticity and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

The changing scene of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Nogo provides a molecular marker for diagnosis of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Treatment with an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of Amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Getting connected in the dopamine system.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Cell therapy for Parkinson's disease: what next?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Increased CRMP2 phosphorylation is observed in Alzheimer's disease; does this tell us anything about disease development?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Presenilin-dependent receptor processing is required for axon guidance

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

iPSC-derived neurons as a higher-throughput readout for autism: promises and pitfalls

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Signals, synapses, and synthesis: how new proteins control plasticity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Axon guidance in the developing ocular motor system and Duane retraction syndrome depends on Semaphorin signaling via alpha2-chimaerin.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

Hippocampal subregion-specific microRNA expression during epileptogenesis in experimental temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970257-1

7 January 2021

10.1016/S1474-4422(14)70257-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25769423%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference