(Q24314592)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference

GOA release 2020-03-11

skeletal system development

1 reference

chondrodysplasia punctata

GOA release 2020-03-11

1 reference

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Christine Petit

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Andrea Ballabio

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

author name string

G Meroni

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

G Parenti

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

J Levilliers

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

L Bernard

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

M Gebbia

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

L Cox

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

P Maroteaux

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

L Sheffield

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

G A Rappold

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

G Andria

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

language of work or name

English

0 references

publication date

1 April 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

volume

81

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

page(s)

15-25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

The warfarin embryopathy: a rat model showing maxillonasal hypoplasia and other skeletal disturbances

24 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Heterogeneity of Chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Maternal and fetal sequelae of anticoagulation during pregnancy

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Action of surface-active agents on arylsulfatase-C of human cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Morquio disease: isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfatase

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfatase

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Chondrodysplasia punctata-23 cases of a mild and relatively common variety

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Characterization of a murine gene expressed from the inactive X chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

A high resolution deletion map of human chromosome Xp22.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

MIC2R: a transcribed MIC2-related sequence associated with a CpG island in the human pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

X chromosome inactivation of the human TIMP gene.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Pattern-induced multi-sequence alignment (PUMA) algorithm employing secondary structure-dependent gap penalties for use in comparative protein modelling

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Multiple sulphatase deficiency presenting at birth

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

cDNA cloning, nucleotide sequence and expression of the gene for arylsulfatase in the sea urchin (Hemicentrotus pulcherrimus) embryo.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Analysis of the Escherichia coli genome: DNA sequence of the region from 84.5 to 86.5 minutes

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

A sulfur- and tyramine-regulated Klebsiella aerogenes operon containing the arylsulfatase (atsA) gene and the atsB gene

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

SR alpha promoter: an efficient and versatile mammalian cDNA expression system composed of the simian virus 40 early promoter and the R-U5 segment of human T-cell leukemia virus type 1 long terminal repeat

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

Mechanism of bone and cartilage maldevelopment in the warfarin embryopathy

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2895%2990367-4

7 January 2021

10.1016/0092-8674(95)90367-4

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7720070%20AND%20SRC:MED&resulttype=core&format=json

release_udm4xw63o5bmbbcmmfj6fht4eu

24 October 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/udm4xw63o5bmbbcmmfj6fht4eu

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017