(Q44606546)

4 December 2017

title

Lack of type XVIII collagen results in anterior ocular defects (English)

1 reference

4 December 2017

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

17 March 2024

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

17 March 2024

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

17 March 2024

9

Taina Pihlajaniemi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525950

17 March 2024

author name string

Ritva Ylikärppä

1

1 reference

4 December 2017

Lauri Eklund

2

1 reference

4 December 2017

Raija Sormunen

3

1 reference

4 December 2017

Aino Utriainen

5

1 reference

4 December 2017

Marko Määttä

6

1 reference

4 December 2017

Naomi Fukai

7

1 reference

4 December 2017

Antti I. Kontiola

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525950

17 March 2024

Björn R. Olsen

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525950

17 March 2024

language of work or name

English

0 references

publication date

2 October 2003

1 reference

full work available at URL

4 December 2017

http://www.fasebj.org/cgi/content/abstract/17/15/2257

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525950

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.02-1001fje

17 March 2024

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

https://onlinelibrary.wiley.com/doi/full-xml/10.1096/fj.02-1001fje

17 March 2024

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

17 March 2024

1 reference

4 December 2017

volume

17

1 reference

4 December 2017

issue

15

1 reference

4 December 2017

page(s)

2257-2259

1 reference

Isolation and sequencing of cDNAs for proteins with multiple domains of Gly-Xaa-Yaa repeats identify a distinct family of collagenous proteins

4 December 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Collagen XVIII is a basement membrane heparan sulfate proteoglycan

17 March 2024

3

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Characterization of the mouse gene for the alpha 1 chain of type XVIII collagen (Col18a1) reveals that the three variant N-terminal polypeptide forms are transcribed from two widely separated promoters

17 March 2024

4

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Endostatin: an endogenous inhibitor of angiogenesis and tumor growth

17 March 2024

5

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Mouse Col18a1 is expressed in a tissue-specific manner as three alternative variants and is localized in basement membrane zones

17 March 2024

6

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

The short and long forms of type XVIII collagen show clear tissue specificities in their expression and location in basement membrane zones in humans

17 March 2024

7

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Epitope-defined monoclonal antibodies against multiplexin collagens demonstrate that type XV and XVIII collagens are expressed in specialized basement membranes

17 March 2024

8

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)

17 March 2024

9

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome

17 March 2024

10

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Lack of collagen XVIII/endostatin results in eye abnormalities

17 March 2024

11

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance.

17 March 2024

13

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Collagen XVIII, a basement membrane heparan sulfate proteoglycan, interacts with L-selectin and monocyte chemoattractant protein-1.

17 March 2024

15

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

The induction/impact tonometer: a new instrument to measure intraocular pressure in the rat

17 March 2024

16

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Method for the noninvasive measurement of intraocular pressure in mice

17 March 2024

17

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Ultrastructure of the iris

17 March 2024

20

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Intercellular junctions of the iris epithelia in Macaca mulatta

17 March 2024

21

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Expression of collagen XVIII and localization of its glycosaminoglycan attachment sites

17 March 2024

23

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Intraocular pressure in inbred mouse strains

17 March 2024

26

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Intraocular pressure in genetically distinct mice: an update and strain survey

17 March 2024

27

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

17 March 2024

28

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice

17 March 2024

29

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance

17 March 2024

31

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Axenfeld-Rieger syndrome in the age of molecular genetics

17 March 2024

32

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Anterior segment dysgenesis and the developmental glaucomas are complex traits

17 March 2024

33

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25

17 March 2024

34

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

17 March 2024

36

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

17 March 2024

37

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome

17 March 2024

39

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

Missense mutation in the alternative splice region of the PAX6 gene in eye anomalies

17 March 2024

40

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

A novel PAX6 gene mutation (P118R) in a family with congenital nystagmus associated with a variant form of aniridia

17 March 2024

41

1 reference

https://api.crossref.org/works/10.1096/FJ.02-1001FJE

17 March 2024

Identifiers

0 references

1 reference