(Q28584708)

GOA release 2020-03-11

1 reference

7

Andrea Superti-Furga

0 references

Haruhiko Koseki

object named as

Haruhiko Koseki

17

0 references

David Rimoin

6

object named as

David L. Rimoin

1 reference

31 January 2017

3

Gen Nishimura

1 reference

31 January 2017

18

Shiro Ikegawa

1 reference

31 January 2017

2

Tatsuya Furuichi

1 reference

31 January 2017

Shuichi Hiraoka

1

1 reference

31 January 2017

Shunichi Shibata

4

1 reference

31 January 2017

Masaki Yanagishita

5

1 reference

31 January 2017

Peter G. Nikkels

8

1 reference

31 January 2017

Minako Ogawa

9

1 reference

31 January 2017

Kayoko Katsuyama

10

1 reference

31 January 2017

Hidenao Toyoda

11

1 reference

31 January 2017

Akiko Kinoshita-Toyoda

12

1 reference

31 January 2017

Nobuhiro Ishida

13

1 reference

31 January 2017

Kyoichi Isono

14

1 reference

31 January 2017

Yutaka Sanai

15

1 reference

31 January 2017

Daniel H. Cohn

16

1 reference

31 January 2017

language of work or name

English

0 references

publication date

1 November 2007

1 reference

31 January 2017

1 reference

31 January 2017

13

1 reference

31 January 2017

11

1 reference

31 January 2017

1363–1367

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31 January 2017

Cartilage proteoglycans

1 reference

7 January 2021

Chondrodysplasias due to proteoglycan defects

1 reference

7 January 2021

Recent advances in the study of the biosynthesis and functions of sulfated glycosaminoglycans

1 reference

7 January 2021

Molecular characterization of human UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter, a novel nucleotide sugar transporter with dual substrate specificity

1 reference

7 January 2021

Variety of nucleotide sugar transporters with respect to the interaction with nucleoside mono- and diphosphates

1 reference

7 January 2021

Chemical and immunological assay of the nonreducing terminal residues of chondroitin sulfate from human aggrecan

1 reference

7 January 2021

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

1 reference

7 January 2021

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse

1 reference

7 January 2021

Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement

1 reference

7 January 2021

Maintenance of chondroitin sulfation balance by chondroitin-4-sulfotransferase 1 is required for chondrocyte development and growth factor signaling during cartilage morphogenesis

1 reference

7 January 2021

Molecular physiology and pathology of the nucleotide sugar transporter family (SLC35)

1 reference

7 January 2021

Structural analysis of glycosaminoglycans in Drosophila and Caenorhabditis elegans and demonstration that tout-velu, a Drosophila gene related to EXT tumor suppressors, affects heparan sulfate in vivo

1 reference

7 January 2021

Biosynthesis of proteoglycan in bone and cartilage of parathyroid hormone-related protein knockout mice.

1 reference

7 January 2021

A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia

1 reference

7 January 2021

Case report 693: Schneckenbecken dysplasia

1 reference

7 January 2021

Schneckenbecken dysplasia, radiology, and histology

1 reference

7 January 2021

Nosology and classification of genetic skeletal disorders: 2006 revision

1 reference

7 January 2021

A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation

1 reference

7 January 2021

Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid

1 reference

7 January 2021

Murine developmental control genes

1 reference

7 January 2021

In situ hybridization and immunohistochemistry of versican, aggrecan and link protein, and histochemistry of hyaluronan in the developing mouse limb bud cartilage

1 reference

7 January 2021