(Q24655619)

21

0 references

Marina Cavazzana

22

Marina Cavazzana-Calvo

0 references

Andrea Ditadi

6

0 references

Emmanuelle M. Six

2

0 references

Frédéric Rieux-Laucat

4

0 references

Laurent Abel

20

0 references

Capucine Picard

3

0 references

Chantal Lagresle-Peyrou

1

Chantal Lagresle-Peyrou

0 references

James C Mullikin

11

James C Mullikin

0 references

Estelle Morillon

8

Estelle Morillon

0 references

Françoise Valensi

9

Françoise Valensi

0 references

author name string

Chantal Lagresle-Peyrou

1

0 references

Vincent Michel

5

0 references

Corinne Demerens-de Chappedelaine

7

0 references

Karen L Simon-Stoos

10

0 references

Lenora M Noroski

12

0 references

Céline Besse

13

0 references

Nicolas M Wulffraat

14

0 references

Alina Ferster

15

0 references

Manuel M Abecasis

16

0 references

Fabien Calvo

17

0 references

Fabio Candotti

Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays

19

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language of work or name

English

0 references

publication date

January 2009

0 references

published in

Nature Genetics

0 references

volume

41

0 references

page(s)

106-11

0 references

issue

1

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Specific ablation of the apoptotic functions of cytochrome C reveals a differential requirement for cytochrome C and Apaf-1 in apoptosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Generation of Epstein-Barr Virus (EBV)-immortalized B cell lines

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

A mutation of human cytochrome c enhances the intrinsic apoptotic pathway but causes only thrombocytopenia.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

A human postnatal lymphoid progenitor capable of circulating and seeding the thymus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

AK2 activates a novel apoptotic pathway through formation of a complex with FADD and caspase-10.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Different mitochondrial intermembrane space proteins are released during apoptosis in a manner that is coordinately initiated but can vary in duration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Dynamics of nucleotide metabolism as a supporter of life phenomena

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Release of adenylate kinase 2 from the mitochondrial intermembrane space during apoptosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

cDNA cloning and tissue-specific expression of the gene encoding human adenylate kinase isozyme 2.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Hax1-mediated processing of HtrA2 by Parl allows survival of lymphocytes and neurons

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Functional characterization of rat ecto-ATPase and ecto-ATP diphosphohydrolase after heterologous expression in CHO cells.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.278

Re-examining the role of cytochrome c in cell death

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.278

Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.278

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612090

Successful cord blood transplantation in a premature and dysmature neonate of 1700 g with reticular dysgenesis

28 November 2018

1 reference

12 December 2020

Successful haploidentical bone marrow transplantation in a patient with reticular dysgenesis: three-year follow-up

1 reference

12 December 2020

Successful bone-marrow transplantation for reticular dysgenesis

1 reference

12 December 2020

Effect of recombinant human granulocyte colony-stimulating factor in reticular dysgenesis

1 reference

12 December 2020

Distinct expression patterns of the p53-homologue p73 in malignant and normal hematopoiesis assessed by a novel real-time reverse transcription-polymerase chain reaction assay and protein analysis

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.278

1 reference

Dimensions Publication ID

2995130

1017849251

0 references

2995130

1 reference

1 reference

1 reference