(Q33907958)

29 July 2017

title

COL4A1 mutation in preterm intraventricular hemorrhage (English)

1 reference

29 July 2017

1

Kaya Bilguvar

1 reference

29 July 2017

Michael L DiLuna

2

1 reference

29 July 2017

Matthew J Bizzarro

3

1 reference

29 July 2017

Yasar Bayri

4

1 reference

29 July 2017

Karen C Schneider

5

1 reference

29 July 2017

Richard P Lifton

6

1 reference

29 July 2017

Murat Gunel

7

1 reference

29 July 2017

Laura R Ment

8

1 reference

29 July 2017

Pacifier and Breastfeeding Trial Group

9

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 November 2009

1 reference

The Journal of Pediatrics

29 July 2017

published in

1 reference

29 July 2017

volume

155

1 reference

29 July 2017

issue

5

1 reference

29 July 2017

page(s)

743-745

1 reference

COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Type IV procollagen missense mutations associated with defects of the eye, vascular stability, the brain, kidney function and embryonic or postnatal viability in the mouse, Mus musculus: an extension of the Col4a1 allelic series and the identificati

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Familial and genetic susceptibility to major neonatal morbidities in preterm twins

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Sequence variants in SLITRK1 are associated with Tourette's syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Organization and expression of basement membrane collagen IV genes and their roles in human disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Long-term outcome after neonatal intraparenchymal echodensities with porencephaly.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Outcome of extremely low birth weight survivors at school age: the influence of perinatal parameters on neurodevelopment

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Mutations of COL10A1 in Schmid metaphyseal chondrodysplasia.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

Collagen IV is essential for basement membrane stability but dispensable for initiation of its assembly during early development

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2884156

The NC1 domain of collagen IV encodes a novel network composed of the alpha 1, alpha 2, alpha 5, and alpha 6 chains in smooth muscle basement membranes

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19840616

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JPEDS.2009.04.014

1 reference

29 July 2017

1 reference

29 July 2017

1 reference