(Q40997100)

25 September 2017

RAD51 haploinsufficiency causes congenital mirror movements in humans (English)

1 reference

25 September 2017

0 references

0 references

Isabelle Dusart

23

0 references

Sergiu Groppa

Sergiu Groppa

5

0 references

Jean-Christophe Corvol

Jean-Christophe Corvol

Kailash Phatechand Bhatia

8

0 references

Kailash Bhatia

11

0 references

Giovanni Stevanin

Giovanni Stevanin

19

0 references

Aurélie Méneret

Aurélie Méneret

3

0 references

Marie Vidailhet

21

Marie Vidailhet

1 reference

25 September 2017

22

Christine Klein

1 reference

25 September 2017

Christel Depienne

1

1 reference

25 September 2017

Delphine Bouteiller

2

1 reference

25 September 2017

Ségolène Billot

4

1 reference

25 September 2017

Stephan Klebe

6

1 reference

25 September 2017

Fanny Charbonnier-Beaupel

7

1 reference

25 September 2017

Jean-Paul Saraiva

9

1 reference

25 September 2017

Norbert Brueggemann

10

1 reference

25 September 2017

Massimo Cincotta

12

1 reference

25 September 2017

Vanessa Brochard

13

1 reference

25 September 2017

Constance Flamand-Roze

14

1 reference

25 September 2017

Wassila Carpentier

15

1 reference

25 September 2017

Sabine Meunier

16

1 reference

25 September 2017

Yannick Marie

17

1 reference

25 September 2017

Marion Gaussen

18

1 reference

25 September 2017

Rosine Wehrle

20

1 reference

25 September 2017

Alexis Brice

24

1 reference

25 September 2017

Emmanuel Roze

25

1 reference

25 September 2017

language of work or name

English

0 references

publication date

2 February 2012

1 reference

American Journal of Human Genetics

25 September 2017

1 reference

25 September 2017

90

1 reference

25 September 2017

2

1 reference

25 September 2017

301-307

1 reference

Congenital mirror movements: a clue to understanding bimanual motor control

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Purified human BRCA2 stimulates RAD51-mediated recombination

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Developmental and benign movement disorders in childhood

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Discovery of a novel function for human Rad51: maintenance of the mitochondrial genome

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

The BRC repeats of BRCA2 modulate the DNA-binding selectivity of RAD51

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Identification of a novel human Rad51 variant that promotes DNA strand exchange

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

The consequences of Rad51 overexpression for normal and tumor cells

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Homologous recombination in DNA repair and DNA damage tolerance

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Human disorders of cortical development: from past to present

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

The RAD51 gene family, genetic instability and cancer

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Molecular views of recombination proteins and their control

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Insights into DNA recombination from the structure of a RAD51-BRCA2 complex

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

BCR/ABL regulates mammalian RecA homologs, resulting in drug resistance

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Xrcc2 is required for genetic stability, embryonic neurogenesis and viability in mice

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Targeted disruption of the Rad51 gene leads to lethality in embryonic mice

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

A novel DCC mutation and genetic heterogeneity in congenital mirror movements.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Mutations in DCC cause congenital mirror movements.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Identification of ventricular-side-enriched molecules regulated in a stage-dependent manner during cerebral cortical development

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

A novel DCC mutation and genetic heterogeneity in congenital mirror movements

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276668

Expression of the Netrin-1 receptor, deleted in colorectal cancer (DCC), is largely confined to projecting neurons in the developing forebrain

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22305526

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identification of Rad51 alteration in patients with bilateral breast cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22305526

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2011.12.002

1 reference

25 September 2017

1 reference

25 September 2017

PubMed publication ID

22305526

1 reference