ALX4 dysfunction disrupts craniofacial and epidermal development (Q24336580)

GOA release 2020-03-11

author

Bernd Wollnik

16

0 references

Hulya Kayserili

1

0 references

author name string

Elif Uz

2

0 references

Carien Niessen

3

0 references

Ibrahim Vargel

4

0 references

Yasemin Alanay

5

0 references

Gokhan Tuncbilek

6

0 references

Gokhan Yigit

7

0 references

Oya Uyguner

8

0 references

Sukru Candan

9

0 references

Hamza Okur

10

0 references

Serkan Kaygin

11

0 references

Sevim Balci

12

0 references

Emin Mavili

13

0 references

Mehmet Alikasifoglu

14

0 references

Ingo Haase

15

0 references

Nurten Ayse Akarsu

Epithelial-mesenchymal interactions in the outgrowth of limb buds and facial primordia in chick embryos

17

0 references

language of work or name

English

0 references

publication date

15 November 2009

0 references

published in

Human Molecular Genetics

0 references

volume

18

0 references

page(s)

4357-66

0 references

issue

22

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Cranial skeletal biology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

21 January 2018

Frontonasal dysplasia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Frontonasal malformation as a field defect and in syndromic associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Frontonasal dysplasia: analysis of 21 cases and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Anatomical classification facial, cranio-facial and latero-facial clefts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Alx-4: cDNA cloning and characterization of a novel paired-type homeodomain protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Alx4 binding to LEF-1 regulates N-CAM promoter activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Median cleft of the upper lip associated with lipomas of the central nervous system and cutaneous polyps.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Two siblings with an unusual nasal malformation: further instances of craniorhiny?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Homeodomain-DNA recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Site-specific heterodimerization by paired class homeodomain proteins mediates selective transcriptional responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Cooperative dimerization of paired class homeo domains on DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Homeodomain revisited: a lesson from disease-causing mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

LMX1B transactivation and expression in nail-patella syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Alx1, a member of the Cart1/Alx3/Alx4 subfamily of Paired-class homeodomain proteins, is an essential component of the gene network controlling skeletogenic fate specification in the sea urchin embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Tight junctions/adherens junctions: basic structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

E-cadherin controls adherens junctions in the epidermis and the renewal of hair follicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Conditional targeting of E-cadherin in skin: insights into hyperproliferative and degenerative responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

Frontonasal "dysplasia," cerebral anomalies, and polydactyly: report of a new syndrome and discussion from a developmental field perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

Noses nobody knows--for real: rhiny and craniorhiny

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

The origin and development of alopecia in mice homozygous for strong's luxoid gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021

A peculiar malformation of the upper lip: report of six cases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP391

7 January 2021