Evidence map›Paper›PMID 34088841›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

The relationship between birth timing, circuit wiring, and physiological response properties of cerebellar granule cells.

S Andrew Shuster, Mark J Wagner, Nathan Pan-Doh, Jing Ren, Sophie M Grutzner, Kevin T Beier, Tony Hyun Kim, Mark J Schnitzer, Liqun Luo

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. The Cerebellar Cortex.Annual review of neuroscience · 2022
    Review
  12. Article
  13. Review
  14. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

S Andrew ShusterHHMI, Stanford University, Stanford, CA 94305.
Mark J WagnerHHMI, Stanford University, Stanford, CA 94305.ORCID 0000-0003-1816-6407
Nathan Pan-DohHHMI, Stanford University, Stanford, CA 94305.ORCID 0000-0001-9317-0209
Jing RenHHMI, Stanford University, Stanford, CA 94305.ORCID 0000-0002-6665-7457
Sophie M GrutznerHHMI, Stanford University, Stanford, CA 94305.
Kevin T BeierHHMI, Stanford University, Stanford, CA 94305.ORCID 0000-0002-4934-1338
Tony Hyun KimHHMI, Stanford University, Stanford, CA 94305.
Mark J SchnitzerHHMI, Stanford University, Stanford, CA 94305.
Liqun LuoHHMI, Stanford University, Stanford, CA 94305; lluo@stanford.edu.ORCID 0000-0001-5467-9264

Funding

Molecular mechanisms of synapse lossR01NS048085 · NINDS · GEORGETOWN UNIVERSITY · PI PAK, DANIEL T · 2006 to 2010
$1.4M
Investigating function of novel drug-induced synaptic changes in the VTAK99DA041445 · NIDA · STANFORD UNIVERSITY · PI BEIER, KEVIN T · 2016 to 2017
$362k
Howard Hughes Medical InstituteNIDA NIH HHS K99 DA041445NINDS NIH HHS R01 NS048085
6 · The paper itself

Abstract

Cerebellar granule cells (GrCs) are usually regarded as a uniform cell type that collectively expands the coding space of the cerebellum by integrating diverse combinations of mossy fiber inputs. Accordingly, stable molecularly or physiologically defined GrC subtypes within a single cerebellar region have not been reported. The only known cellular property that distinguishes otherwise homogeneous GrCs is the correspondence between GrC birth timing and the depth of the molecular layer to which their axons project. To determine the role birth timing plays in GrC wiring and function, we developed genetic strategies to access early- and late-born GrCs. We initiated retrograde monosynaptic rabies virus tracing from control (birth timing unrestricted), early-born, and late-born GrCs, revealing the different patterns of mossy fiber input to GrCs in vermis lobule 6 and simplex, as well as to early- and late-born GrCs of vermis lobule 6: sensory and motor nuclei provide more input to early-born GrCs, while basal pontine and cerebellar nuclei provide more input to late-born GrCs. In vivo multidepth two-photon Ca

Indexed as

AnimalsAnimals, NewbornCerebellar CortexMiceMice, TransgenicNerve FibersRabies virusbirth timingcerebellumgranule cellsrabies tracingtwo-photon Ca2+ imaging

Identifiers

PMID34088841
PMCPMC8201928

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.