X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (19) 19
humans (15) 15
versican (14) 14
female (12) 12
male (12) 12
cspg2 gene (11) 11
cspg2 (9) 9
disease (9) 9
ophthalmology (9) 9
family (8) 8
pedigree (8) 8
versicans - genetics (8) 8
biochemistry & molecular biology (7) 7
identification (7) 7
site mutation (7) 7
adult (6) 6
aged (6) 6
erosive vitreoretinopathy (6) 6
expression (6) 6
mutation (6) 6
versicans - deficiency (6) 6
animals (5) 5
proteoglycan (5) 5
retinal degeneration - genetics (5) 5
vcan (5) 5
versicans (5) 5
gene cspg2 (4) 4
genes (4) 4
genetics & heredity (4) 4
mice (4) 4
middle aged (4) 4
phenotype (4) 4
retina (4) 4
retinal degeneration - diagnosis (4) 4
analysis (3) 3
biology (3) 3
child (3) 3
chondroitin sulfate proteoglycans - genetics (3) 3
exons (3) 3
eye (3) 3
eye diseases - genetics (3) 3
gene expression (3) 3
genetic research (3) 3
genetics (3) 3
genotype (3) 3
growth (3) 3
hyaluronan (3) 3
medicine & public health (3) 3
pg-m (3) 3
proteoglycans (3) 3
rna splice sites - genetics (3) 3
versicans - metabolism (3) 3
visual acuity (3) 3
vitreous body - pathology (3) 3
wagner syndrome (3) 3
3t3 cells (2) 2
adhesion (2) 2
adolescent (2) 2
aged, 80 and over (2) 2
aggrecan (2) 2
binding (2) 2
case-control studies (2) 2
cell biology (2) 2
child, preschool (2) 2
chondrogenesis (2) 2
chondroitin sulfate (2) 2
chondroitin sulfate proteoglycan (2) 2
chromosomes, human, pair 5 - genetics (2) 2
collagen (2) 2
degeneration (2) 2
deletion (2) 2
developmental biology (2) 2
dna, recombinant (2) 2
electroretinography (2) 2
exudative vitreoretinopathy (2) 2
fundus oculi (2) 2
g3 domain (2) 2
gene expression regulation, developmental (2) 2
genetic association (2) 2
genetic association studies (2) 2
genetic predisposition to disease (2) 2
glycosaminoglycans (2) 2
haploinsufficiency (2) 2
haplotypes (2) 2
intestinal-type gastric cancer (2) 2
intracranial aneurysm (2) 2
lectins, c-type (2) 2
lectins, c-type - genetics (2) 2
link protein (2) 2
linkage (2) 2
matrix (2) 2
medical research (2) 2
medicine, experimental (2) 2
mesoderm - cytology (2) 2
mice, transgenic (2) 2
mutation - genetics (2) 2
polymorphism, single nucleotide (2) 2
proteins (2) 2
region (2) 2
research article (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2018, Volume 176, Issue 8, pp. 1778 - 1783
Wagner syndrome and erosive vitreoretinopathy together constitute the phenotypic continuum of an autosomal dominant vitreoretinopathy, with clinical findings... 
Deletion | versican | VCAN | Wagner syndrome | vitreoretinopathy | SITE MUTATION | IDENTIFICATION | EROSIVE VITREORETINOPATHY | FAMILY | DISEASE | BIOLOGY | GENETICS & HEREDITY | STICKLER-SYNDROME | CSPG2 GENE | Medicine, Experimental | Genetic research | Medical research | Genes | Retina | DNA microarrays | Clonal deletion | Collagen (type II) | Versican | Haploinsufficiency
Journal Article
Journal of Cancer Research and Clinical Oncology, ISSN 0171-5216, 02/2010, Volume 136, Issue 2, pp. 195 - 201
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 1/2018, Volume 256, Issue 1, pp. 163 - 171
Journal Article
Ophthalmic Surgery Lasers and Imaging Retina, ISSN 2325-8160, 06/2016, Volume 47, Issue 6, pp. 574 - 579
Journal Article
by Zhang, Y and Cao, L and Yang, BL and Yang, BB
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 08/1998, Volume 273, Issue 33, pp. 21342 - 21351
Versican is a member of the large aggregating chondroitin sulfate proteoglycan family. We have expressed in NIH3T3 fibroblasts a recombinant versican mini-gene... 
PG-M VERSICAN | CHONDROITIN SULFATE PROTEOGLYCANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHENOTYPE | RECEPTOR | LINK PROTEIN | TISSUES | GENE CSPG2 | SUBSTRATUM ADHESION | 3T3 CELLS | TENASCIN-R
Journal Article
Molecular Vision, ISSN 1090-0535, 2011, Volume 17, Issue 184-85, pp. 1669 - 1678
Journal Article
東京女子医科大学雑誌, ISSN 0040-9022, 2012, Volume 82, Issue 3, pp. 162 - 171
[緒言]心臓は, 胚発生において最初に形成される非常に重要な臓器の一つである. 先天性心疾患は出生1,000人に対し約4~10人の割合で生じるが1), ヒトの先天異常による胎生致死の多くは心血管奇形が原因であり, この中でも特に流出路異常に関連するものが多い2).... 
Journal Article
No res