The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11.

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.

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.

Who cites it

13 citing papers in PubMed, 30 citations in OpenAlex.

1. Cancer and Radiosensitivity Syndromes: Is Impaired Nuclear ATM Kinase Activity the Primum Movens?Cancers · 2022
   Review
2. A single synonymous mutation determines the phosphorylation and stability of the nascent protein.Journal of molecular cell biology · 2019
   Article
3. Yeast XRS2 and human NBN gene: Experimental evidence for homology using codon optimized cDNA.PloS one · 2018
   Article
4. ATM-mediated mitochondrial damage response triggered by nuclear DNA damage in normal human lung fibroblasts.Cell cycle (Georgetown, Tex.) · 2017
   Article
5. NBS1 and multiple regulations of DNA damage response.Journal of radiation research · 2016
   Review
6. Nijmegen breakage syndrome gene, NBS1, and molecular links to factors for genome stability.Oncogene · 2002
   Review
7. Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group.Archives of disease in childhood · 2000
   Review
8. Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.American journal of human genetics · 1998
   Article
9. Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation.Molecular and cellular biology · 1997
   Article
10. Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.American journal of human genetics · 1997
    Article
11. Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.American journal of human genetics · 1997
    Article
12. The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.American journal of human genetics · 1997
    Article
13. A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity.Journal of medical genetics · 1997
    Article

Corrections and comments

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

Authors and funding

8 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as