XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination. (Q39696233)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27281794%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

title

XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination (English)

1 reference

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13 March 2020

6

1 reference

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13 March 2020

Dik C van Gent

17

1 reference

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13 March 2020

Jacques Van Dongen

18

1 reference

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13 March 2020

Jacques Van Dongen

19

1 reference

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13 March 2020

Mirjam van der Burg

20

1 reference

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13 March 2020

Myriam Ricarda Lorenz

11

object named as

Myriam Lorenz

1 reference

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13 March 2020

author name string

Hanna IJspeert

1

1 reference

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13 March 2020

Jacob Rozmus

2

1 reference

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13 March 2020

Klaus Schwarz

3

1 reference

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13 March 2020

René L Warren

4

1 reference

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13 March 2020

David van Zessen

5

1 reference

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13 March 2020

Ingrid Pico-Knijnenburg

7

1 reference

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13 March 2020

Erik Simons

8

1 reference

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13 March 2020

Isabel Jerchel

9

1 reference

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13 March 2020

Angela Wawer

10

1 reference

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13 March 2020

Turkan Patıroğlu

12

1 reference

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13 March 2020

Himmet Haluk Akar

13

1 reference

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13 March 2020

Ricardo Leite

14

1 reference

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13 March 2020

Nicole S Verkaik

15

1 reference

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13 March 2020

Andrew P Stubbs

16

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13 March 2020

language of work or name

English

0 references

publication date

8 June 2016

1 reference

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13 March 2020

1 reference

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13 March 2020

volume

128

1 reference

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13 March 2020

issue

5

1 reference

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13 March 2020

page(s)

650-659

1 reference

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RAG2 and XLF/Cernunnos interplay reveals a novel role for the RAG complex in DNA repair

13 March 2020

cites work

1 reference

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Timely and spatially regulated maturation of B and T cell repertoire during human fetal development

14 September 2017

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Interactome analysis identifies a new paralogue of XRCC4 in non-homologous end joining DNA repair pathway

14 September 2017

1 reference

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DNA repair. PAXX, a paralog of XRCC4 and XLF, interacts with Ku to promote DNA double-strand break repair

14 September 2017

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ImmunoGlobulin galaxy (IGGalaxy) for simple determination and quantitation of immunoglobulin heavy chain rearrangements from NGS

14 September 2017

1 reference

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Hematopoietic stem cell dysfunction underlies the progressive lymphocytopenia in XLF/Cernunnos deficiency

14 September 2017

1 reference

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Extreme growth failure is a common presentation of ligase IV deficiency

14 September 2017

1 reference

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PRKDC mutations in a SCID patient with profound neurological abnormalities

14 September 2017

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Cernunnos deficiency reduces thymocyte life span and alters the T cell repertoire in mice and humans

14 September 2017

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IMGT(®) tools for the nucleotide analysis of immunoglobulin (IG) and T cell receptor (TR) V-(D)-J repertoires, polymorphisms, and IG mutations: IMGT/V-QUEST and IMGT/HighV-QUEST for NGS.

14 September 2017

1 reference

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Cernunnos influences human immunoglobulin class switch recombination and may be associated with B cell lymphomagenesis

14 September 2017

1 reference

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A human XRCC4-XLF complex bridges DNA

14 September 2017

1 reference

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Non-homologous end-joining partners in a helical dance: structural studies of XLF-XRCC4 interactions

14 September 2017

1 reference

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XRCC4 Protein Interactions with XRCC4-like Factor (XLF) Create an Extended Grooved Scaffold for DNA Ligation and Double Strand Break Repair

14 September 2017

1 reference

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Structural characterization of filaments formed by human Xrcc4-Cernunnos/XLF complex involved in nonhomologous DNA end-joining

14 September 2017

1 reference

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Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency

14 September 2017

1 reference

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Exhaustive T-cell repertoire sequencing of human peripheral blood samples reveals signatures of antigen selection and a directly measured repertoire size of at least 1 million clonotypes.

14 September 2017

1 reference

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A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

14 September 2017

1 reference

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Lymphocyte-specific compensation for XLF/cernunnos end-joining functions in V(D)J recombination

14 September 2017

1 reference

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Role and regulation of human XRCC4-like factor/cernunnos

14 September 2017

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Cernunnos/XLF promotes the ligation of mismatched and noncohesive DNA ends

14 September 2017

1 reference

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Nonoverlapping functions of DNA polymerases mu, lambda, and terminal deoxynucleotidyltransferase during immunoglobulin V(D)J recombination in vivo

14 September 2017

1 reference

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XLF interacts with the XRCC4-DNA ligase IV complex to promote DNA nonhomologous end-joining

14 September 2017

1 reference

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Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly

14 September 2017

1 reference

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A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

14 September 2017

1 reference

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A biochemically defined system for mammalian nonhomologous DNA end joining

14 September 2017

1 reference

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The mechanism of non-homologous end-joining: a synopsis of synapsis

14 September 2017

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An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome

14 September 2017

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Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936.

14 September 2017

1 reference

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Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study

14 September 2017

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Immunoglobulin kappa light chain gene rearrangement is impaired in mice deficient for DNA polymerase mu

14 September 2017

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Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair

14 September 2017

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Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination

14 September 2017

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Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

14 September 2017

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Ku80 is required for addition of N nucleotides to V(D)J recombination junctions by terminal deoxynucleotidyl transferase

14 September 2017

1 reference

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Chromosomal stability and the DNA double-stranded break connection

14 September 2017

1 reference

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The DNA-dependent protein kinase

14 September 2017

1 reference

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Absence of DNA ligase IV protein in XR-1 cells: evidence for stabilization by XRCC4.

14 September 2017

1 reference

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Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes

14 September 2017

1 reference

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Mutational analysis of residues in the nucleotide binding domain of human terminal deoxynucleotidyl transferase

14 September 2017

1 reference

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Initiation of V(D)J recombination in a cell-free system.

14 September 2017

1 reference

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The mechanism of V(D)J recombination: a balance of diversity, specificity, and stability

14 September 2017

1 reference

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RAG mutations in human B cell-negative SCID.

14 September 2017

1 reference

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Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency

25 September 2017

1 reference

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Clinical spectrum of LIG4 deficiency is broadened with severe dysmaturity, primordial dwarfism, and neurological abnormalities

17 June 2018

1 reference

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Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.

17 June 2018

1 reference

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Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia

17 June 2018

1 reference

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Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype.

17 June 2018

1 reference

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Defective Artemis nuclease is characterized by coding joints with microhomology in long palindromic-nucleotide stretches

20 August 2018

1 reference

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The use of non-natural nucleotides to probe template-independent DNA synthesis.

20 August 2018

1 reference

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New insights on human T cell development by quantitative T cell receptor gene rearrangement studies and gene expression profiling.

20 August 2018

1 reference

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The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG-deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins.

20 August 2018

1 reference

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Cleavage at a V(D)J recombination signal requires only RAG1 and RAG2 proteins and occurs in two steps

20 August 2018

1 reference

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Insertion of N regions into heavy-chain genes is correlated with expression of terminal deoxytransferase in B cells

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4974199

Ig gene rearrangement steps are initiated in early human precursor B cell subsets and correlate with specific transcription factor expression

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27281794

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27281794

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

V(D)J Recombination in Ku86-Deficient Mice: Distinct Effects on Coding, Signal, and Hybrid Joint Formation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27281794

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2016-02-701029

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27281794%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27281794%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

PubMed publication ID

27281794

1 reference