(Q24336580)

GOA release 2020-03-11

author

Bernd Wollnik

16

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Hulya Kayserili

1

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author name string

Elif Uz

2

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Carien Niessen

3

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Ibrahim Vargel

4

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Yasemin Alanay

5

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Gokhan Tuncbilek

6

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Gokhan Yigit

7

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Oya Uyguner

8

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Sukru Candan

9

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Hamza Okur

10

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Serkan Kaygin

11

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Sevim Balci

12

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Emin Mavili

13

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Mehmet Alikasifoglu

14

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Ingo Haase

15

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Nurten Ayse Akarsu

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

17

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language of work or name

English

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publication date

15 November 2009

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published in

Human Molecular Genetics

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volume

18

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issue

22

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page(s)

4357-66

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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