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Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.20589openalex-snapshot

Presence of neurotrophic factors in skeletal muscle correlates with survival of spinal cord motor neurons

inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.011openalex-snapshot

Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.013openalex-snapshot

Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance

inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.018openalex-snapshot

Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia

inferredcites →https://doi.org/10.1016/j.cmet.2011.01.010openalex-snapshot

Melanocortin-4 Receptors Expressed by Cholinergic Neurons Regulate Energy Balance and Glucose Homeostasis

inferredcites →https://doi.org/10.1016/j.devcel.2007.06.010openalex-snapshot

Rab6 Regulates Transport and Targeting of Exocytotic Carriers

inferredcites →https://doi.org/10.1016/j.jneumeth.2014.02.005openalex-snapshot

Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles

inferredcites →https://doi.org/10.1016/j.nmd.2016.09.009openalex-snapshot

Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria

inferredcites →https://doi.org/10.1016/j.tcb.2016.01.001openalex-snapshot

Bicaudal D Family of Motor Adaptors: Linking Dynein Motility to Cargo Binding

inferredcites →https://doi.org/10.1016/j.tins.2013.08.001openalex-snapshot

Cytoplasmic dynein heavy chain: the servant of many masters

inferredcites →https://doi.org/10.1016/j.tins.2018.07.006openalex-snapshot

Walking Forward with Kinesin

inferredcites →https://doi.org/10.1016/j.ydbio.2009.05.554openalex-snapshot

Progenitors of skeletal muscle satellite cells express the muscle determination gene, MyoD

inferredcites →https://doi.org/10.1038/ejhg.2017.98openalex-snapshot

Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features

inferredcites →https://doi.org/10.1038/emboj.2010.78openalex-snapshot

The more, the better: the BICD family gets bigger

inferredcites →https://doi.org/10.1038/ncb2067openalex-snapshot

Rab and actomyosin-dependent fission of transport vesicles at the Golgi complex

inferredcites →https://doi.org/10.1038/ncb891openalex-snapshot

Bicaudal-D regulates COPI-independent Golgi–ER transport by recruiting the dynein–dynactin motor complex

inferredcites →https://doi.org/10.1038/ncomms4411openalex-snapshot

A role for Bicaudal-D2 in radial cerebellar granule cell migration

inferredcites →https://doi.org/10.1038/s41582-019-0257-2openalex-snapshot

Axonal transport and neurological disease

inferredcites →https://doi.org/10.1073/pnas.0805422105openalex-snapshot

Mutant dynein (Loa) triggers proprioceptive axon loss that extends survival only in the SOD1 ALS model with highest motor neuron death

inferredcites →https://doi.org/10.1073/pnas.1614557114openalex-snapshot

Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations

inferredcites →https://doi.org/10.1073/pnas.1620141114openalex-snapshot

DYNC1H1 mutations associated with neurological diseases compromise processivity of dynein–dynactin–cargo adaptor complexes

inferredcites →https://doi.org/10.1083/jcb.147.4.743openalex-snapshot

Rab6 Coordinates a Novel Golgi to ER Retrograde Transport Pathway in Live Cells

inferredcites →https://doi.org/10.1083/jcb.201703201openalex-snapshot

Disease-associated mutations in human BICD2 hyperactivate motility of dynein–dynactin

inferredcites →https://doi.org/10.1083/jcb.201805002openalex-snapshot

RAB6 and microtubules restrict protein secretion to focal adhesions

inferredcites →https://doi.org/10.1093/brain/aws108openalex-snapshot

Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells

inferredcites →https://doi.org/10.1093/brain/awu356openalex-snapshot

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

inferredcites →https://doi.org/10.1093/emboj/20.15.4041openalex-snapshot

Mammalian Golgi‐associated Bicaudal‐D2 functions in the dynein–dynactin pathway by interacting with these complexes

inferredcites →https://doi.org/10.1093/hmg/ddy086openalex-snapshot

Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development

inferredcites →https://doi.org/10.1095/biolreprod.108.071175openalex-snapshot

GPR30 Does Not Mediate Estrogenic Responses in Reproductive Organs in Mice

inferredcites →https://doi.org/10.1111/boc.201400083openalex-snapshot

Phenotypic characterisation of RAB6A knockout mouse embryonic fibroblasts

inferredcites →https://doi.org/10.1126/science.1083129openalex-snapshot

Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135722openalex-snapshot

Motor Neuron Diversity in Development and Disease

inferredcites →https://doi.org/10.1186/s13104-016-1915-8openalex-snapshot

A simple, step-by-step dissection protocol for the rapid isolation of mouse dorsal root ganglia

inferredcites →https://doi.org/10.1186/s13395-018-0171-0openalex-snapshot

MuscleJ: a high-content analysis method to study skeletal muscle with a new Fiji tool

inferredcites →https://doi.org/10.1212/wnl.0000000000001269openalex-snapshot

Novel mutations expand the clinical spectrum of DYNC1H1 -associated spinal muscular atrophy

inferredcites →https://doi.org/10.1212/wnl.0000000000003360openalex-snapshot

Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement

inferredcites →https://doi.org/10.1212/wnl.0b013e3182556c05openalex-snapshot

Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy

inferredcites →https://doi.org/10.1371/journal.pone.0075902openalex-snapshot

Neuron-Type Specific Functions of DNT1, DNT2 and Spz at the Drosophila Neuromuscular Junction

inferredcites →https://doi.org/10.1523/jneurosci.4338-07.2007openalex-snapshot

Proprioceptive Sensory Neuropathy in Mice with a Mutation in the Cytoplasmic Dynein Heavy Chain 1 Gene

inferredcites →https://doi.org/10.15252/embj.201387579openalex-snapshot

Bicaudal‐D1 regulates the intracellular sorting and signalling of neurotrophin receptors

inferredcites →https://doi.org/10.15252/embj.201488698openalex-snapshot

Negative control of BAK1 by protein phosphatase 2A during plant innate immunity

inferredcites →https://doi.org/10.3389/fncel.2014.00140openalex-snapshot

siRNA screen of ES cell-derived motor neurons identifies novel regulators of tetanus toxin and neurotrophin receptor trafficking

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/bies.202300052openalex-snapshot

JNK‐interacting protein 4 is a central molecule for lysosomal retrograde trafficking

inferred← citeshttps://doi.org/10.1038/s12276-024-01200-7openalex-snapshot

Cargo specificity, regulation, and therapeutic potential of cytoplasmic dynein

inferred← citeshttps://doi.org/10.1097/gco.0000000000000661openalex-snapshot

Gene expression in urinary incontinence and pelvic organ prolapse: a review of literature

inferred← citeshttps://doi.org/10.1186/s13104-020-05147-6openalex-snapshot

A video protocol for rapid dissection of mouse dorsal root ganglia from defined spinal levels

inferred← citeshttps://doi.org/10.5582/irdr.2021.01004openalex-snapshot

A novel BICD2 mutation of a patient with Spinal Muscular Atrophy Lower Extremity Predominant 2

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