(Q24321595)

embryonic cranial skeleton morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

10

Hülya Kayserili

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Stanley F Nelson

6

object named as

Stanley F Nelson

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author name string

Carine Bonnard

1

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Anna C Strobl

2

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Mohammad Shboul

3

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Hane Lee

4

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Barry Merriman

5

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Osama H Ababneh

7

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Elif Uz

8

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Tülay Güran

9

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Hanan Hamamy

11

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Bruno Reversade

Neural Crest and the Origin of Vertebrates: A New Head

12

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language of work or name

English

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publication date

June 2012

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published in

Nature Genetics

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volume

44

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issue

6

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page(s)

709-13

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cites work

1 reference

Mutations in PYCR1 cause cutis laxa with progeroid features

20 April 2017

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Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling

20 April 2017

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The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient

20 April 2017

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Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

20 April 2017

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GATA3 haplo-insufficiency causes human HDR syndrome

20 April 2017

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Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2

20 April 2017

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The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development

20 April 2017

1 reference

ALX4 dysfunction disrupts craniofacial and epidermal development

20 April 2017

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Role of the neural crest in face and brain development

20 April 2017

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The neural crest and neural crest cells: discovery and significance for theories of embryonic organization

21 January 2018

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Genetics of craniofacial development and malformation

21 January 2018

1 reference

Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: new syndrome?

21 January 2018

1 reference

Homeodomain revisited: a lesson from disease-causing mutations

21 January 2018

1 reference

The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx.

21 January 2018

1 reference

Collective chemotaxis requires contact-dependent cell polarity.

21 January 2018

1 reference

Functional characterization of SDF-1 proximal promoter

21 January 2018

1 reference

Analysis of SDF-1/CXCR4 signaling in primordial germ cell migration and survival or differentiation in Xenopus laevis

21 January 2018

1 reference

miRNA regulation of Sdf1 chemokine signaling provides genetic robustness to germ cell migration

21 January 2018

1 reference

Celsius: a community resource for Affymetrix microarray data

21 January 2018

1 reference

Interaction between transcription factors Iroquois proteins 4 and 5 controls cardiac potassium channel Kv4.2 gene transcription

21 January 2018

1 reference

Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1.

21 January 2018

1 reference

Adult and two children with fetal methotrexate syndrome

21 January 2018

1 reference

Acquired variation outweighs inherited variation in whole genome analysis of methotrexate polyglutamate accumulation in leukemia

21 January 2018

1 reference

Mutations in different components of FGF signaling in LADD syndrome

21 January 2018

1 reference

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing

21 January 2018

1 reference

SeqWare Query Engine: storing and searching sequence data in the cloud

21 January 2018

1 reference

The Iroquois family of genes: from body building to neural patterning.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22581230

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22581230