(Q38178068)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24419271%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

title

Neurobiology of autism gene products: towards pathogenesis and drug targets (English)

1 reference

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5 March 2020

0 references

0 references

6

1 reference

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5 March 2020

Dilja Krueger-Burg

3

1 reference

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5 March 2020

Peter Scheiffele

5

1 reference

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5 March 2020

7

Nils Brose

1 reference

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5 March 2020

author name string

Kristel T E Kleijer

1

1 reference

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5 March 2020

Michael J Schmeisser

2

1 reference

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5 March 2020

Tobias M Boeckers

4

1 reference

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5 March 2020

J Peter H Burbach

8

1 reference

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5 March 2020

publication date

14 January 2014

1 reference

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5 March 2020

1 reference

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5 March 2020

volume

231

1 reference

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5 March 2020

issue

6

1 reference

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5 March 2020

page(s)

1037-1062

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Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice

5 March 2020

cites work

1 reference

12 December 2020

The diuretic bumetanide decreases autistic behaviour in five infants treated during 3 months with no side effects.

1 reference

12 December 2020

PTEN and myotubularin: novel phosphoinositide phosphatases

1 reference

12 December 2020

Behavioural phenotyping assays for mouse models of autism

1 reference

12 December 2020

Deregulation of EIF4E: a novel mechanism for autism.

1 reference

12 December 2020

Cre/loxP-mediated inactivation of the murine Pten tumor suppressor gene.

1 reference

12 December 2020

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

1 reference

12 December 2020

Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina

1 reference

12 December 2020

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

1 reference

12 December 2020

PTEN signaling in brain: neuropathology and tumorigenesis.

1 reference

12 December 2020

Genetic causes of syndromic and non-syndromic autism

1 reference

12 December 2020

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

1 reference

12 December 2020

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

1 reference

12 December 2020

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

1 reference

12 December 2020

SHANK1 Deletions in Males with Autism Spectrum Disorder

1 reference

12 December 2020

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

1 reference

12 December 2020

Pten is essential for embryonic development and tumour suppression

1 reference

12 December 2020

Endocannabinoid-mediated control of synaptic transmission

1 reference

12 December 2020

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

1 reference

12 December 2020

Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

1 reference

12 December 2020

Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism

1 reference

12 December 2020

Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay

1 reference

12 December 2020

The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

1 reference

12 December 2020

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

1 reference

12 December 2020

Impact of acamprosate on behavior and brain-derived neurotrophic factor: an open-label study in youth with fragile X syndrome

1 reference

12 December 2020

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

1 reference

12 December 2020

Negative regulation of neural stem/progenitor cell proliferation by the Pten tumor suppressor gene in vivo

1 reference

12 December 2020

EU-AIMS: a boost to autism research.

1 reference

12 December 2020

Disorder-associated mutations lead to functional inactivation of neuroligins

1 reference

12 December 2020

Functional consequences of mutations in postsynaptic scaffolding proteins and relevance to psychiatric disorders.

1 reference

12 December 2020

Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53

1 reference

12 December 2020

Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism

1 reference

12 December 2020

Chronic pharmacological mGlu5 inhibition corrects fragile X in adult mice

1 reference

12 December 2020

Chemical probes of endocannabinoid metabolism

1 reference

12 December 2020

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

1 reference

12 December 2020

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

1 reference

12 December 2020

Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4.

1 reference

12 December 2020

The Autistic Neuron: Troubled Translation?

1 reference

12 December 2020

The local differentiation of myelinated axons at nodes of Ranvier

1 reference

12 December 2020

Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons

1 reference

12 December 2020

Hypersensitivity to mGluR5 and ERK1/2 leads to excessive protein synthesis in the hippocampus of a mouse model of fragile X syndrome

1 reference

12 December 2020

Homodimerization and isoform-specific heterodimerization of neuroligins

1 reference

12 December 2020

PTEN deletion in Bergmann glia leads to premature differentiation and affects laminar organization

1 reference

12 December 2020

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

1 reference

12 December 2020

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis

1 reference

12 December 2020

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies.

1 reference

12 December 2020

Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.

1 reference

12 December 2020

PTEN hamartoma tumor syndrome: an overview

1 reference

12 December 2020

What does CNTNAP2 reveal about autism spectrum disorder?

1 reference

12 December 2020

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

1 reference

12 December 2020

Rescue of dendritic spine phenotype in Fmr1 KO mice with the mGluR5 antagonist AFQ056/Mavoglurant

1 reference

12 December 2020

Modeling human disease in humans: the ciliopathies

1 reference

12 December 2020

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

1 reference

12 December 2020

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

1 reference

12 December 2020

Novel de novo SHANK3 mutation in autistic patients

1 reference

12 December 2020

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

1 reference

12 December 2020

A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export

1 reference

12 December 2020

Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling

1 reference

12 December 2020

Timothy syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons

1 reference

12 December 2020

Deletion of alpha-neurexins does not cause a major impairment of axonal pathfinding or synapse formation

1 reference

12 December 2020

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.

1 reference

12 December 2020

Correction of fragile X syndrome in mice.

1 reference

12 December 2020

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments

1 reference

12 December 2020

Pten regulates neuronal arborization and social interaction in mice

1 reference

12 December 2020

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

1 reference

12 December 2020

Association of common variants in the Joubert syndrome gene (AHI1) with autism

1 reference

12 December 2020

Abnormal network activity in a targeted genetic model of human double cortex

1 reference

12 December 2020

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

1 reference

12 December 2020

mTor is required for hypertrophy of Pten-deficient neuronal soma in vivo

1 reference

12 December 2020

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development

1 reference

12 December 2020

Sociability and motor functions in Shank1 mutant mice

1 reference

12 December 2020

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

1 reference

12 December 2020

Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.

1 reference

12 December 2020

A copy number variation morbidity map of developmental delay

1 reference

12 December 2020

Exaggerated translation causes synaptic and behavioural aberrations associated with autism

1 reference

12 December 2020

A role for primary cilia in glutamatergic synaptic integration of adult-born neurons

1 reference

12 December 2020

The conundrums of understanding genetic risks for autism spectrum disorders

1 reference

12 December 2020

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

12 December 2020

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

1 reference

12 December 2020

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

1 reference

12 December 2020

Rapamycin for treating Tuberous sclerosis and Autism spectrum disorders

1 reference

12 December 2020

An architectural framework that may lie at the core of the postsynaptic density

1 reference

12 December 2020

Postsynaptic scaffolding molecules modulate the localization of neuroligins

1 reference

12 December 2020

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills

1 reference

12 December 2020

Progress toward treatments for synaptic defects in autism

1 reference

12 December 2020

SnapShot: mTOR signaling

1 reference

12 December 2020

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

1 reference

12 December 2020

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders

1 reference

12 December 2020

Lovastatin corrects excess protein synthesis and prevents epileptogenesis in a mouse model of fragile X syndrome

1 reference

12 December 2020

Scaffold proteins at the postsynaptic density

1 reference

12 December 2020

Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease

1 reference

12 December 2020

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders

1 reference

12 December 2020

Fragile X: translation in action

1 reference

12 December 2020

The role of neurexins and neuroligins in the formation, maturation, and function of vertebrate synapses

1 reference

12 December 2020

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

1 reference

12 December 2020

A randomised controlled trial of bumetanide in the treatment of autism in children

1 reference

12 December 2020

FMRP targets distinct mRNA sequence elements to regulate protein expression

1 reference

12 December 2020

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

12 December 2020

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

1 reference

12 December 2020

High cancer susceptibility and embryonic lethality associated with mutation of the PTEN tumor suppressor gene in mice

1 reference

12 December 2020

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

1 reference

12 December 2020

Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.

1 reference

12 December 2020

Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice

1 reference

12 December 2020

Phenotypic checkpoints regulate neuronal development.

1 reference

12 December 2020

Neuroligins determine synapse maturation and function

1 reference

12 December 2020

PTEN function: how normal cells control it and tumour cells lose it

1 reference

12 December 2020

Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.

1 reference

12 December 2020

Phosphatase and tensin homologue (PTEN) regulates synaptic plasticity independently of its effect on neuronal morphology and migration

1 reference

12 December 2020

Neuroligin-1-dependent competition regulates cortical synaptogenesis and synapse number

1 reference

12 December 2020

Pten loss causes hypertrophy and increased proliferation of astrocytes in vivo

1 reference

12 December 2020

Neuroligin-3 is a neuronal adhesion protein at GABAergic and glutamatergic synapses

1 reference

12 December 2020

Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.

1 reference

12 December 2020

Synapse- and stimulus-specific local translation during long-term neuronal plasticity

1 reference

12 December 2020

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

1 reference

12 December 2020

Modeling autism by SHANK gene mutations in mice

1 reference

12 December 2020

Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities

1 reference

12 December 2020

Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.

1 reference

12 December 2020

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

1 reference

12 December 2020

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

1 reference

12 December 2020

Higher-order architecture of cell adhesion mediated by polymorphic synaptic adhesion molecules neurexin and neuroligin

1 reference

12 December 2020

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 reference

12 December 2020

Translational animal models of autism and neurodevelopmental disorders.

1 reference

12 December 2020

Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior

1 reference

12 December 2020

Control of excitatory and inhibitory synapse formation by neuroligins

1 reference

12 December 2020

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice

1 reference

12 December 2020

Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function

1 reference

12 December 2020

PTEN signaling in autism spectrum disorders

1 reference

12 December 2020

eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation

1 reference

12 December 2020

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice

1 reference

12 December 2020

1 reference

12 December 2020

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)

1 reference

12 December 2020

The story of Rett syndrome: from clinic to neurobiology

1 reference

12 December 2020

Activity-dependent neuronal signalling and autism spectrum disorder

1 reference

12 December 2020

Function of PTEN during the formation and maintenance of neuronal circuits in the brain

1 reference

12 December 2020

A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins

1 reference

12 December 2020

Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses

1 reference

12 December 2020

1 reference

12 December 2020

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

12 December 2020

Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses

1 reference

12 December 2020

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

1 reference

12 December 2020

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

1 reference

12 December 2020

Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density

1 reference

12 December 2020

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

1 reference

12 December 2020

An epigenetic framework for neurodevelopmental disorders: from pathogenesis to potential therapy

1 reference

12 December 2020

Topoisomerases facilitate transcription of long genes linked to autism

1 reference

12 December 2020

PTEN: a tumour suppressor that functions as a phospholipid phosphatase

1 reference

12 December 2020

Genetic advances in autism: heterogeneity and convergence on shared pathways

1 reference

12 December 2020

Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism.

1 reference

12 December 2020

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

1 reference

12 December 2020

Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology

1 reference

12 December 2020

The GABA excitatory/inhibitory shift in brain maturation and neurological disorders

1 reference

12 December 2020

SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.

1 reference

12 December 2020

Phosphatase and tensin homolog, deleted on chromosome 10 deficiency in brain causes defects in synaptic structure, transmission and plasticity, and myelination abnormalities

1 reference

12 December 2020

PTEN: from pathology to biology

1 reference

12 December 2020

Studying autism in rodent models: reconciling endophenotypes with comorbidities

1 reference

12 December 2020

Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2.

1 reference

12 December 2020

Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease

1 reference

12 December 2020

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

1 reference

12 December 2020

Reversal of neurological defects in a mouse model of Rett syndrome

1 reference

12 December 2020

Neuroligins and neurexins link synaptic function to cognitive disease

1 reference

12 December 2020

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2

1 reference

12 December 2020

Contribution of SHANK3 mutations to autism spectrum disorder

1 reference

12 December 2020

PTEN hamartoma tumor syndromes.

1 reference

12 December 2020

Altered synchrony and connectivity in neuronal networks expressing an autism-related mutation of neuroligin 3

1 reference

12 December 2020

Connecting genes to brain in the autism spectrum disorders

1 reference

12 December 2020

Targeted treatment trials for tuberous sclerosis and autism: no longer a dream

1 reference

12 December 2020

Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism

1 reference

12 December 2020

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

1 reference

12 December 2020

Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation

1 reference

12 December 2020

Refuting the challenges of the developmental shift of polarity of GABA actions: GABA more exciting than ever!

1 reference

12 December 2020

Animal models of autism spectrum disorder (ASD): a synaptic-level approach to autistic-like behavior in mice

1 reference

12 December 2020

The role of neurexins in schizophrenia and autistic spectrum disorder.

1 reference

12 December 2020

ProSAP/Shank proteins - a family of higher order organizing molecules of the postsynaptic density with an emerging role in human neurological disease

1 reference

12 December 2020

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

1 reference

12 December 2020

PTEN is essential for cell migration but not for fate determination and tumourigenesis in the cerebellum

1 reference

12 December 2020

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.

1 reference

12 December 2020

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.

1 reference

12 December 2020

Mutations affecting synaptic levels of neurexin-1β in autism and mental retardation

1 reference

12 December 2020

Ion channel functional candidate genes in multigenic neuropsychiatric disease

1 reference

12 December 2020

The Shank family of scaffold proteins

1 reference

12 December 2020

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

1 reference

12 December 2020

Selective deletion of PTEN in dopamine neurons leads to trophic effects and adaptation of striatal medium spiny projecting neurons

1 reference

12 December 2020

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

1 reference

12 December 2020

Congenital disorders of glycosylation: a rapidly expanding disease family

1 reference

12 December 2020

Animal models of autism with a particular focus on the neural basis of changes in social behaviour: an update article

1 reference

12 December 2020

Synapse pathology in psychiatric and neurologic disease

1 reference

12 December 2020

Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation

1 reference

12 December 2020

Pten deletion causes mTorc1-dependent ectopic neuroblast differentiation without causing uniform migration defects

1 reference

12 December 2020

Targeting the endocannabinoid system in the treatment of fragile X syndrome.

1 reference

12 December 2020

Identification of a novel cortactin SH3 domain-binding protein and its localization to growth cones of cultured neurons

1 reference

12 December 2020

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

1 reference

12 December 2020

Mutations causing syndromic autism define an axis of synaptic pathophysiology

1 reference

12 December 2020

Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level

1 reference

12 December 2020

Assessing behavioural and cognitive domains of autism spectrum disorders in rodents: current status and future perspectives

1 reference

12 December 2020

From genes to cognition in tuberous sclerosis: implications for mTOR inhibitor-based treatment approaches

1 reference

12 December 2020

Environmental factors in autism

1 reference

12 December 2020

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

1 reference

12 December 2020

Pten ablation in adult dopaminergic neurons is neuroprotective in Parkinson's disease models.

1 reference

12 December 2020

An open-label naturalistic pilot study of acamprosate in youth with autistic disorder

1 reference

12 December 2020

From mTOR to cognition: molecular and cellular mechanisms of cognitive impairments in tuberous sclerosis

1 reference

12 December 2020

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

1 reference

12 December 2020

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

12 December 2020

The mGluR theory of fragile X mental retardation

1 reference

12 December 2020

Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci.

1 reference

12 December 2020

Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders

1 reference

12 December 2020

Reversing neurodevelopmental disorders in adults

1 reference

12 December 2020

Autism risk factors: genes, environment, and gene-environment interactions

1 reference

12 December 2020

Genetic architecture in autism spectrum disorder

1 reference

12 December 2020

10.1007/S00213-013-3403-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24419271%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 March 2020

1027815946

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Fatcat ID

release_qf7ei6x2y5ggvft5ovgiake5ui

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qf7ei6x2y5ggvft5ovgiake5ui

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24419271%20AND%20SRC:MED&resulttype=core&format=json