(Q24305935)

craniofacial suture morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

6

Daniela F Bueno

Daniela F

Bueno

1 reference

19 October 2023

Luis G Alonso

5

Luis G

Alonso

1 reference

Andrew Oliver Mungo Wilkie

19 October 2023

Andrew O M Wilkie

18

Andrew O M

Wilkie

1 reference

19 October 2023

Dominik Seelow

2

Dominik

Seelow

1 reference

19 October 2023

Maria Rita Passos-Bueno

17

object named as

Maria Rita Passos-Bueno

Maria Rita

Passos-Bueno

1 reference

19 October 2023

Dagan Jenkins

1

Dagan

Jenkins

1 reference

19 October 2023

Fernanda S Jehee

3

Fernanda S

Jehee

1 reference

19 October 2023

Chad A Perlyn

4

Chad A

Perlyn

1 reference

19 October 2023

Dian Donnai

7

Dian

Donnai

1 reference

19 October 2023

Dragana Josifova

8

Dragana

Josifova

1 reference

19 October 2023

Dragana Josifiova

9

0 references

Irene M J Mathijssen

10

Irene M J

Mathijssen

1 reference

19 October 2023

Jenny E V Morton

11

Jenny E V

Morton

1 reference

19 October 2023

Karen Helene Orstavik

12

Karen Helene

Orstavik

1 reference

19 October 2023

Elizabeth Sweeney

13

Elizabeth

Sweeney

1 reference

19 October 2023

Steven A Wall

14

Steven A

Wall

1 reference

19 October 2023

Jeffrey L Marsh

15

Jeffrey L

Marsh

1 reference

19 October 2023

Peter Nurnberg

16

Peter

Nurnberg

1 reference

American Journal of Human Genetics

19 October 2023

language of work or name

English

0 references

publication date

June 2007

0 references

published in

0 references

volume

80

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issue

6

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page(s)

1162-70

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cites work

Acrocephaly, with other Congenital Malformations

1 reference

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Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

19 March 2017

1 reference

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A haplotype map of the human genome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Structural basis of family-wide Rab GTPase recognition by rabenosyn-5

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

A phenotype-based screen for embryonic lethal mutations in the mouse

19 March 2017

1 reference

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The Ciliopathies: An Emerging Class of Human Genetic Disorders

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Craniofacial dysmorphology of Carpenter syndrome: lessons from three affected siblings

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Signaling from Smo to Ci/Gli: conservation and divergence of Hedgehog pathways from Drosophila to vertebrates

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Twist plays an essential role in FGF and SHH signal transduction during mouse limb development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Evolution of the Rab family of small GTP-binding proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Open brain gene product Rab23: expression pattern in the adult mouse brain and functional characterization

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Mouse Rab23 regulates hedgehog signaling from smoothened to Gli proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Hedgehog signalling in the mouse requires intraflagellar transport proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

FGF-, BMP- and Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Open brain, a new mouse mutant with severe neural tube defects, shows altered gene expression patterns in the developing spinal cord

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

The chicken talpid3 gene encodes a novel protein essential for Hedgehog signaling

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Hedgehog signaling and congenital malformations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Rab23, a negative regulator of hedgehog signaling, localizes to the plasma membrane and the endocytic pathway

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Isolation of a mouse cDNA encoding Rab23, a small novel GTPase expressed predominantly in the brain

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive 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=1867103

A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Dorsal and lateral fates in the mouse neural tube require the cell-autonomous activity of the open brain 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=1867103

Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

29 November 2018

New drugs from fat bugs?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

The mammalian Rab family of small GTPases: definition of family and subfamily sequence motifs suggests a mechanism for functional specificity in the Ras superfamily.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

BMP5 and the molecular, skeletal, and soft-tissue alterations in short ear mice

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Carpenter syndrome: natural history and clinical spectrum

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867103

Expression of the Hedgehog antagonists Rab23 and Slimb/βTrCP during mouse tooth development

29 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/17503333

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Expression patterns of Hedgehog signalling pathway members during mouse palate development

1 reference

https://pubmed.ncbi.nlm.nih.gov/17503333

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/518047

0 references

Fatcat ID

release_g7ubwukx5fcwxps2okt4x3al2q

0 references

PMC publication ID

1867103

0 references