Evidence map›Paper›PMID 15060138›Full record

ArticleMolecular and cellular biology2004

Generation and characterization of LANP/pp32 null mice.

Puneet Opal, Jesus J Garcia, Alanna E McCall, Bisong Xu, Edwin J Weeber, J David Sweatt, Harry T Orr, Huda Y Zoghbi

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cracking the ANP32 whips: important functions, unequal requirement, and hints at disease implications.BioEssays : news and reviews in molecular, cellular and developmental biology · 2014
    Article
  11. Article
  12. Article
  13. Article
  14. Acidic nuclear phosphoprotein 32kDa (ANP32)B-deficient mouse reveals a hierarchy of ANP32 importance in mammalian development.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors at 3 institutions in 1 country.

Puneet OpalDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA. p-opal@northwestern.edu
Jesus J Garcia
Alanna E McCall
Bisong Xu
Edwin J Weeber
J David Sweatt
Harry T Orr
Huda Y Zoghbi
Baylor College of Medicine · USHoward Hughes Medical Institute · USUniversity of Minnesota · US

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI BEAUDET, ARTHUR L. · 1988 to 2013
$29.4M
MOLECULAR STUDIES OF SPINOCEREBELLAR ATAXIA TYPE 1R01NS027699 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI HUDA Y ZOGHBI · 1989 to 2026
$8.8M
UNDERSTANDING SPINOCEREBELLAR ATAXIA TYPE 1 PATHOGENESISK08NS002246 · NINDS · NORTHWESTERN UNIVERSITY · PI OPAL, PUNEET · 2000 to 2005
$760k
NICHD NIH HHS HD24064NICHD NIH HHS P30 HD024064NINDS NIH HHS K08 NS002246NINDS NIH HHS K08 NS02246-03NINDS NIH HHS R01 NS027699NINDS NIH HHS R01 NS27699-13
6 · The paper itself

Abstract

The leucine-rich acidic nuclear protein (LANP) belongs to a family of evolutionarily conserved proteins that are characterized by an amino-terminal domain rich in leucine residues followed by a carboxy-terminal acidic tail. LANP has been implicated in the regulation of a variety of cellular processes including RNA transport, transcription, apoptosis, vesicular trafficking, and intracellular signaling. Abundantly expressed in the developing cerebellum, this protein has also been hypothesized to play a role in cerebellar morphogenesis. LANP has been implicated in disease biology as well, both as a mediator of toxicity in spinocerebellar ataxia type 1 and as a tumor suppressor in cancers of the breast and prostate. To better understand the function of this multifaceted protein, we have generated mice lacking LANP. Surprisingly, these mice are viable and fertile. In addition we could not discern any derangements in any of the major organ systems, including the nervous system, which we have studied in detail. Overall our results point to a functional redundancy of LANP's function, most likely provided by its closely related family members.

Indexed as

AnimalsBehavior, AnimalBrainElectrophysiologyFemaleFetal ViabilityGene TargetingHumansImmunohistochemistryIn Vitro TechniquesMiceMice, Inbred C57BLMice, KnockoutNeuropeptidesNuclear ProteinsPhosphoproteinsANP32B protein, humanNeuropeptidesNuclear ProteinsPhosphoproteins

Identifiers

PMID15060138
PMCPMC381670
OpenAlexW2124209162

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.