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Pathogenesis of hemangioma
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Pathogenesis of hemangioma
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
author
Douglas A Marchuk
1 reference
stated in
ORCID Public Data File 2021
author name string
D A Marchuk
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
language of work or name
English
0 references
publication date
1 March 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
volume
107
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
page(s)
665-666
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
cites work
Clonality and altered behavior of endothelial cells from hemangiomas.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
GLUT1: a newly discovered immunohistochemical marker for juvenile hemangiomas
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Vascular endothelial growth factor confers a growth advantage in vitro and in vivo to stromal cells cultured from neonatal hemangiomas
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Cellular markers that distinguish the phases of hemangioma during infancy and childhood
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
Endothelioma cells expressing the polyoma middle T oncogene induce hemangiomas by host cell recruitment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
5 July 2018
A unique microvascular phenotype shared by juvenile hemangiomas and human placenta.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
28 October 2018
Hemangioma in twins.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208951
retrieved
28 October 2018
Genetic mapping of a novel familial form of infantile hemangioma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased apoptosis coincides with onset of involution in infantile hemangioma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Progressive growth of infantile cutaneous hemangiomas is directly correlated with hyperplasia and angiogenesis of adjacent epidermis and inversely correlated with expression of the endogenous angiogenesis inhibitor, IFN-beta
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
An increased incidence of haemangiomas in infants born following chorionic villus sampling (CVS)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11254664
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI12470
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
PMCID
208951
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
PubMed ID
11254664
1 reference
stated in
Europe PubMed Central
PubMed ID
11254664
retrieved
31 July 2017
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