(Q24540185)

6 July 2017

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene (English)

1 reference

6 July 2017

1 reference

P Scambler

7

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author name string

D M Hagan

1

1 reference

6 July 2017

A J Ross

2

1 reference

6 July 2017

T Strachan

3

1 reference

6 July 2017

S A Lynch

4

1 reference

6 July 2017

V Ruiz-Perez

5

1 reference

6 July 2017

Y M Wang

6

1 reference

6 July 2017

E Custard

8

1 reference

6 July 2017

W Reardon

9

1 reference

6 July 2017

S Hassan

10

1 reference

6 July 2017

P Nixon

11

1 reference

6 July 2017

C Papapetrou

12

1 reference

6 July 2017

R M Winter

13

1 reference

6 July 2017

Y Edwards

14

1 reference

6 July 2017

K Morrison

15

1 reference

6 July 2017

M Barrow

16

1 reference

6 July 2017

M P Cordier-Alex

17

1 reference

6 July 2017

P Correia

18

1 reference

6 July 2017

P A Galvin-Parton

19

1 reference

6 July 2017

S Gaskill

20

1 reference

6 July 2017

K J Gaskin

21

1 reference

6 July 2017

S Garcia-Minaur

22

1 reference

6 July 2017

R Gereige

23

1 reference

6 July 2017

R Hayward

24

1 reference

6 July 2017

T Homfray

25

1 reference

6 July 2017

language of work or name

English

0 references

publication date

4 April 2000

1 reference

American Journal of Human Genetics

6 July 2017

1 reference

6 July 2017

66

1 reference

6 July 2017

1504-1515

1 reference

6 July 2017

5

1 reference

Involvement of the HLXB9 homeobox gene in Currarino syndrome

6 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Partial V(D)J recombination activity leads to Omenn syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Characterization of the LIM/homeodomain gene islet-1 and single nucleotide screening in NIDDM

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Requirement for the homeobox gene Hb9 in the consolidation of motor neuron identity

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Selective agenesis of the dorsal pancreas in mice lacking homeobox gene Hlxb9

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Specification of motor neuron identity by the MNR2 homeodomain protein

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Isolated sacral agenesis in a fetus monosomic for 7q36.1-->qter

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Dorsal-ventral patterning during neural induction in Xenopus: assessment of spinal cord regionalization with xHB9, a marker for the motor neuron region

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Case reports of malformations associated with maternal diabetes: history and critique

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A review of caudal dysgenesis and its pathogenesis as illustrated in an animal model.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Homeodomain-DNA recognition

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Active suppression of interneuron programs within developing motor neurons revealed by analysis of homeodomain factor HB9.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Human post-implantation embryo collection: medical and surgical techniques.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Highly restricted expression at the ectoderm-endoderm boundary of PIHbox 9, a sea urchin homeobox gene related to the human HB9 gene.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Functional dissection of a transcriptionally active, target-specific Hox-Pbx complex

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Occult spinal dysraphism: a series of 73 cases

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Pancreas dorsal lobe agenesis and abnormal islets of Langerhans in Hlxb9-deficient mice.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Holoprosencephaly: from Homer to Hedgehog.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

The Currarino triad: its importance in pediatric neurosurgery

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

Triad of anorectal, sacral, and presacral anomalies

29 November 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378009

29 November 2018

https://api.crossref.org/works/10.1086%2F302899

7 January 2021

inferred from DOI database lookup

Partial sacral agenesis with constipation: a report of one family

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10749657

12 December 2020

inferred from PubMed ID database lookup

Sacrum abnormalities and neural tube closure defect: different manifestations of a same genetic disease?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10749657

12 December 2020

inferred from PubMed ID database lookup

Sacral agenesis and caudal spinal cord malformations

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302899

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302899

1 reference

6 July 2017

1 reference

6 July 2017

1 reference