(Q28145744)

English

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium

scientific article (publication date: 25 May 2000)

In more languages

Statements

scholarly article

0 references

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium (English)

0 references

1 reference

based on heuristic

inferred from title

6

0 references

Teresa Esposito

object named as

T Esposito

13

0 references

Fernando Gianfrancesco

object named as

F Gianfrancesco

15

0 references

object named as

P Vabres

3

0 references

object named as

S Wiemann

11

0 references

author name string

A Smahi

1

0 references

G Courtois

2

0 references

S Yamaoka

4

0 references

S Heuertz

5

0 references

A Israël

7

0 references

N S Heiss

8

0 references

S M Klauck

9

0 references

P Kioschis

10

0 references

A Poustka

12

0 references

T Bardaro

14

0 references

A Ciccodicola

16

0 references

M D'Urso

17

0 references

H Woffendin

18

0 references

T Jakins

19

0 references

D Donnai

20

0 references

H Stewart

21

0 references

S J Kenwrick

22

0 references

S Aradhya

23

0 references

T Yamagata

24

0 references

M Levy

25

0 references

R A Lewis

26

0 references

D L Nelson

27

0 references

language of work or name

0 references

publication date

25 May 2000

0 references

0 references

405

0 references

466-72

0 references

6785

0 references

Incontinentia pigmenti (Bloch-Sulzberger syndrome).

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2.

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

IKK-gamma is an essential regulatory subunit of the IkappaB kinase complex

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

IkappaB kinase (IKK)-associated protein 1, a common component of the heterogeneous IKK complex

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

The IKK complex: an integrator of all signals that activate NF-kappaB?

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Complementation cloning of NEMO, a component of the IkappaB kinase complex essential for NF-kappaB activation

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Identification of a cell protein (FIP-3) as a modulator of NF-kappaB activity and as a target of an adenovirus inhibitor of tumor necrosis factor alpha-induced apoptosis

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Sex-dependent rearrangements resulting in CMT1A and HNPP.

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Suppression of TNF-alpha-induced apoptosis by NF-kappaB

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Embryonic lethality and liver degeneration in mice lacking the RelA component of NF-kappa B

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Absence of tumor necrosis factor rescues RelA-deficient mice from embryonic lethality

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Genetic approaches to study Rel/NF-kappa B/I kappa B function in mice

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Requirement for NF-kappaB in osteoclast and B-cell development

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

IKK1-deficient mice exhibit abnormal development of skin and skeleton

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Limb and skin abnormalities in mice lacking IKKalpha

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

The precursor of NF-kappa B p50 has I kappa B-like functions

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Regulation of IkappaBbeta degradation. Similarities to and differences from IkappaBalpha

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

Characterization of a mutant cell line that does not activate NF-kappaB in response to multiple stimuli

1 reference

https://api.crossref.org/works/10.1038%2F35013114

21 January 2018

The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28

1 reference

https://api.crossref.org/works/10.1038%2F35013114

7 January 2021

based on heuristic

inferred from DOI database lookup

The NF-kappa B activation pathway: a paradigm in information transfer from membrane to nucleus

1 reference

https://api.crossref.org/works/10.1038%2F35013114

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

https://api.crossref.org/works/10.1038%2F35013114

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid detection of sequence polymorphisms in the human mitochondrial DNA control region by polymerase chain reaction and single-strand conformation analysis in mutation detection enhancement gels

1 reference

https://api.crossref.org/works/10.1038%2F35013114

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/35013114

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Dimensions Publication ID

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Springer Nature article ID

10.1038/35013114

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28145744&oldid=1833555968"