GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome
about
Expression of glypican-4 in haematopoietic-progenitor and bone-marrow-stromal cellsMapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome.Genetic considerations in the prenatal diagnosis of overgrowth syndromesGlypican-6, a new member of the glypican family of cell surface heparan sulfate proteoglycansGenome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest.The human obesity gene map: the 2000 update.The human obesity gene map: the 2001 update.Evidence for a role of developmental genes in the origin of obesity and body fat distributionEarly identification of risk factors for sudden cardiac death.The human obesity gene map: the 2002 update.Fine-tuning of cell signaling by glypicans.Heparan sulfate proteoglycans: a GAGgle of skeletal-hematopoietic regulators.Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.IFN-beta pharmacogenomics in multiple sclerosis.Boning up on glypicans--opportunities for new insights into bone biology.Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature.Down-regulation of insulin-like growth factor binding protein-5 (IGFBP-5): novel marker for cervical carcinogenesis.Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.In-Depth Proteomic Analysis of the Hippocampus in a Rat Model after Cerebral Ischaemic Injury and Repair by Danhong Injection (DHI).Mechanical strain regulation of the chicken glypican-4 gene expression in the avian eggshell gland.Cartilage ultrastructure in proteoglycan-deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders.Review of X-linked syndromes with arthrogryposis or early contractures-aid to diagnosis and pathway identification.Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.A patient with a unique frameshift mutation in GPC3, causing Simpson-Golabi-Behmel syndrome, presenting with craniosynostosis, penoscrotal hypospadias, and a large prostatic utricleThe Human Obesity Gene Map: The 2004 UpdatePaternal germline mosaicism for aGPC3deletion in X-linked Simpson-Golabi-Behmel syndrome
P2860
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P2860
GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@ast
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en-gb
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@nl
type
label
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@ast
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en-gb
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@nl
prefLabel
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@ast
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en-gb
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@nl
P2093
P356
P1433
P1476
GPC4, the gene for human K-gly ...... Simpson-Golabi-Behmel syndrome
@en
P2093
J Vermeesch
K Watanabe
M Veugelers
Y Yamaguchi
P356
10.1006/GENO.1998.5465
P407
P577
1998-10-01T00:00:00Z