Evidence map›Paper›PMID 10762538›Full record

ArticleAmerican journal of human genetics2000

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

M Alders, A Ryan, M Hodges, J Bliek, A P Feinberg, O Privitera, A Westerveld, P F Little, M Mannens

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  3. Review
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  6. Article
  7. The evolution of reproduction-related NLRP genes.Journal of molecular evolution · 2014
    Article
  8. Article
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  15. High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  16. The SCAN domain of ZNF174 is a dimer.The Journal of biological chemistry · 2002
    Article
  17. Genomic analysis of orthologous mouse and human olfactory receptor loci.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  18. All in the family: the BTB/POZ, KRAB, and SCAN domains.Molecular and cellular biology · 2001
    Review
  19. 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

9 authors at 4 institutions in 4 countries.

M AldersDepartment of Human Genetics and Department of Clinical Genetics, Academic Medical Center, 1105 AZ Amsterdam, The Netherlands.
A Ryan
M Hodges
J Bliek
A P Feinberg
O Privitera
A Westerveld
P F Little
M Mannens
Amsterdam UMC Location University of Amsterdam · NLImperial College London · GBAzienda Ospedaliera Ospedale Civile di Legnano · ITJohns Hopkins University · US

Funding

MOLECULAR PATHOLOGY OF WILMS TUMOR RELATED GENES 11PR01CA054358 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDREW P. FEINBERG · 1991 to 2026
$5.5M
BWS and Embryonal Tumor Suppressor Genes on 11p15R37CA054358 · NCI · JOHNS HOPKINS UNIVERSITY · PI FEINBERG, ANDREW P. · 2001 to 2009
$4.0M
NCI NIH HHS CA54358NCI NIH HHS R01 CA054358
6 · The paper itself

Abstract

The genetics of Beckwith-Wiedemann syndrome (BWS) is complex and is thought to involve multiple genes. It is known that three regions on chromosome 11p15 (BWSCR1, BWSCR2, and BWSCR3) may play a role in the development of BWS. BWSCR2 is defined by two BWS breakpoints. Here we describe the cloning and sequence analysis of 73 kb containing BWSCR2. Within this region, we detected a novel zinc-finger gene, ZNF215. We show that two of its five alternatively spliced transcripts are disrupted by both BWSCR2 breakpoints. Parts of the 3' end of these splice forms are transcribed from the antisense strand of a second zinc-finger gene, ZNF214. We show that ZNF215 is imprinted in a tissue-specific manner.

Indexed as

Zinc FingersAllelesAlternative SplicingAmino Acid SequenceAmino Acid SubstitutionBeckwith-Wiedemann SyndromeCell LineChromosome BreakageChromosomes, Human, Pair 11Cloning, MolecularContig MappingDNA-Binding ProteinsDNA Mutational AnalysisFemaleFetusGenomic ImprintingDNA-Binding ProteinsRNA, AntisenseRNA, MessengerZNF214 protein, humanZNF215 protein, human

Identifiers

PMID10762538
PMCPMC1378011
OpenAlexW2078057618

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.