Irx1 and Irx2 are coordinately expressed and regulated by retinoic acid, TGFβ and FGF signaling during chick hindlimb development (Q21090784)

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Irx1 and Irx2 Are Coordinately Expressed and Regulated by Retinoic Acid, TGFβ and FGF Signaling during Chick Hindlimb Development

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English	Irx1 and Irx2 are coordinately expressed and regulated by retinoic acid, TGFβ and FGF signaling during chick hindlimb development	scientific article	Irx1 and Irx2 Are Coordinately Expressed and Regulated by Retinoic Acid, TGFβ and FGF Signaling during Chick Hindlimb Development

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scholarly article

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Irx1 and Irx2 are coordinately expressed and regulated by retinoic acid, TGFβ and FGF signaling during chick hindlimb development (English)

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1 reference

based on heuristic

inferred from title

author name string

Martha Elena Díaz-Hernández

1

author given names

Martha Elena

author last names

Díaz-Hernández

1 reference

9 August 2022

Marcia Bustamante

2

author given names

Marcia

author last names

Bustamante

1 reference

9 August 2022

Claudio Iván Galván-Hernández

3

author given names

Claudio Iván

author last names

Galván-Hernández

1 reference

9 August 2022

Jesús Chimal-Monroy

4

author given names

Jesús

author last names

Chimal-Monroy

1 reference

9 August 2022

language of work or name

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publication date

2013

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8

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3

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e58549

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copyright license

Creative Commons Attribution 4.0 International

11 March 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

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The BMP antagonist Gremlin regulates outgrowth, chondrogenesis and programmed cell death in the developing limb

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Activator-inhibitor dynamics of vertebrate limb pattern formation

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A series of normal stages in the development of the chick embryo. 1951

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The zebrafish homeobox gene irxl1 is required for brain and pharyngeal arch morphogenesis

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The chemical basis of morphogenesis. 1953.

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30 May 2018

Activin/TGFbeta and BMP crosstalk determines digit chondrogenesis

1 reference

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21 January 2018

Analysis of the molecular cascade responsible for mesodermal limb chondrogenesis: Sox genes and BMP signaling.

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Progressive interdigital cell death: regulation by the antagonistic interaction between fibroblast growth factor 8 and retinoic acid

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BMP signals control limb bud interdigital programmed cell death by regulating FGF signaling.

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An evolutionarily conserved three-dimensional structure in the vertebrate Irx clusters facilitates enhancer sharing and coregulation.

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c-Irx2 expression reveals an early subdivision of the neural plate in the chick embryo.

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21 January 2018

Xiro-1 controls mesoderm patterning by repressing bmp-4 expression in the Spemann organizer.

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Comparison of Iroquois gene expression in limbs/fins of vertebrate embryos.

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Expression pattern of Irx1 and Irx2 during mouse digit development.

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The Fused toes (Ft) mouse mutation causes anteroposterior and dorsoventral polydactyly.

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21 January 2018

Formation of posterior cranial placode derivatives requires the Iroquois transcription factor irx4a

1 reference

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21 January 2018

Growth arrest specific gene 1 acts as a region-specific mediator of the Fgf10/Fgf8 regulatory loop in the limb.

1 reference

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29 November 2018

The Wnt-activated Xiro1 gene encodes a repressor that is essential for neural development and downregulates Bmp4.

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Retinoic acid regulates programmed cell death through BMP signalling.

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Role of BMP-2 and OP-1 (BMP-7) in programmed cell death and skeletogenesis during chick limb development.

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Role of FGFs in the control of programmed cell death during limb development

1 reference

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Gene and cluster-specific expression of the Iroquois family members during mouse development

1 reference

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inferred from PubMed ID database lookup

The mouse Fused toes (Ft) mutation is the result of a 1.6-Mb deletion including the entire Iroquois B gene cluster

1 reference

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inferred from PubMed ID database lookup

Iroquois genes influence proximo-distal morphogenesis during rat lung development

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Smad8 is expressed in the anterior necrotic zone: evidence for a role of bone morphogenetic proteins/SMAD signaling in the activation of a molecular cascade that culminates in cell death

1 reference

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12 December 2020

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10.1371/JOURNAL.PONE.0058549

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2013PLoSO...858549D

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