(Q24306285)

negative regulation of canonical Wnt signaling pathway

GOA release 2020-03-11

1 reference

Cenani-Lenz syndactyly syndrome

GOA release 2020-03-11

1 reference

23

0 references

Gudrun Nürnberg

9

0 references

Bernd Wollnik

26

0 references

Jill Clayton-Smith

21

0 references

Gökhan Yigit

6

0 references

Hulya Kayserili

5

Hülya Kayserili

0 references

Raoul Hennekam

22

Raoul Hennekam

0 references

Khalda S. Amr

Khalda Amr

14

0 references

Jill E. Urquhart

Jill Urquhart

11

0 references

Samira Ismail

Samira Ismail

13

0 references

Mona S Aglan

Mona Aglan

4

0 references

Samia A Temtamy

Samia A Temtamy

25

0 references

Christian Becker

16

Christian Becker

0 references

author name string

Yun Li

1

0 references

Barbara Pawlik

2

0 references

Nursel Elcioglu

3

0 references

Ferda Percin

7

0 references

Frances Goodman

8

0 references

Asim Cenani

10

0 references

Boi-Dinh Chung

12

0 references

Ayca D Aslanger

15

0 references

Christian Netzer

17

0 references

Pete Scambler

18

0 references

Wafaa Eyaid

19

0 references

Hanan Hamamy

20

0 references

Joachim Herz

American Journal of Human Genetics

24

0 references

language of work or name

English

0 references

publication date

14 May 2010

0 references

published in

0 references

volume

86

0 references

issue

5

0 references

page(s)

696-706

0 references

cites work

Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Wnt/beta-catenin signaling in development and disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

New sequence variants associated with bone mineral density

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Lrp4 is a receptor for Agrin and forms a complex with MuSK

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Ectodermal Wnt3/beta-catenin signaling is required for the establishment and maintenance of the apical ectodermal ridge

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

An LDL-receptor-related protein mediates Wnt signalling in mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Lrp4, a novel receptor for Dickkopf 1 and sclerostin, is expressed by osteoblasts and regulates bone growth and turnover in vivo

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Lrp4 modulates extracellular integration of cell signaling pathways in development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

LRP6 mutation in a family with early coronary disease and metabolic risk factors

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Orchestrating ontogenesis: variations on a theme by sonic hedgehog

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

ALOHOMORA: a tool for linkage analysis using 10K SNP array data

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Mild facial dysmorphism and quasidominant inheritance in Cenani-Lenz syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Pattern formation: old models out on a limb.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Patterning mechanisms controlling vertebrate limb development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Dermatoglyphics in patients with Cenani-Lenz type syndactyly: studies in a new case

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Total syndactylia and total radioulnar synostosis in 2 brothers. A contribution on the genetics of syndactylia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Cenani-Lenz syndactyly with facial dysmorphism, hypothyroidism, and renal hypoplasia: a case report

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Defective splicing of Megf7/Lrp4, a regulator of distal limb development, in autosomal recessive mulefoot disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Two unusual types of syndactyly in the same family; Cenani-Lenz type and "new" type versus severe type I syndactyly?

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

A variant of Cenani-Lenz type syndactyly.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869043

GRR: graphical representation of relationship errors

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20381006

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

HaploPainter: a tool for drawing pedigrees with complex haplotypes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20381006

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2010.03.004

1 reference

287267

287267

1 reference

1 reference

1 reference