(Q28219080)

1

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Muriel Durand

2

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Soledad Lopez

3

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Laurence Suel

4

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Josiane Demignon

5

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Charles Thornton

6

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Hidenori Ozaki

7

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Kyoshi Kawakami

8

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Patrick Barbet

9

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Jacques S Beckmann

10

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Pascal Maire

Journal of Muscle Research & Cell Motility

11

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language of work or name

English

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publication date

2002

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published in

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volume

23

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issue

3

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page(s)

255-64

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255-264

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cites work

EGF receptor and Notch signaling act upstream of Eyeless/Pax6 to control eye specification.

1 reference

12 December 2020

PAX-genes expression during human embryonic development, a preliminary report.

1 reference

12 December 2020

Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy

1 reference

12 December 2020

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

1 reference

12 December 2020

Structure, function and expression of a murine homeobox protein AREC3, a homologue of Drosophila sine oculis gene product, and implication in development

1 reference

12 December 2020

The four populations of myoblasts involved in human limb muscle formation are present from the onset of primary myotube formation.

1 reference

12 December 2020

cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene.

1 reference

12 December 2020

Muscle maturation delay in infantile myotonic dystrophy

1 reference

12 December 2020

The birth of muscle progenitor cells in the mouse: spatiotemporal considerations

1 reference

12 December 2020

Skeletal muscle formation in vertebrates

1 reference

12 December 2020

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

1 reference

12 December 2020

Lineage restriction of the myogenic conversion factor myf-5 in the brain

1 reference

12 December 2020

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies

1 reference

12 December 2020

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)

1 reference

12 December 2020

The homeobox protein Six3 interacts with the Groucho corepressor and acts as a transcriptional repressor in eye and forebrain formation

1 reference

12 December 2020

Structure and chromosome mapping of the human SIX4 and murine Six4 genes

1 reference

12 December 2020

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

1 reference

12 December 2020

Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

1 reference

12 December 2020

Calpain3 expression during human cardiogenesis.

1 reference

12 December 2020

The eye-specification proteins So and Eya form a complex and regulate multiple steps in Drosophila eye development

1 reference

12 December 2020

Expression and function of clift in the development of somatic gonadal precursors within the Drosophila mesoderm.

1 reference

12 December 2020

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

1 reference

12 December 2020

Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM

1 reference

12 December 2020

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

1 reference

12 December 2020

Six family genes--structure and function as transcription factors and their roles in development

1 reference

12 December 2020

Homeobox genes and connective tissue patterning

1 reference

12 December 2020

Making muscle in mammals

1 reference

12 December 2020

Antagonism between extradenticle function and Hedgehog signalling in the developing limb

1 reference

12 December 2020

Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development.

1 reference

12 December 2020

Six4, a putative myogenin gene regulator, is not essential for mouse embryonal development.

1 reference

12 December 2020

The alpha subunits of Gz and Gi interact with the eyes absent transcription cofactor Eya2, preventing its interaction with the six class of homeodomain-containing proteins

1 reference

12 December 2020

Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya

1 reference

12 December 2020

MyoD, myogenin independent differentiation of primordial myoblasts in mouse somites

1 reference

12 December 2020

Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin

1 reference

12 December 2020

The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system

1 reference

12 December 2020

A combination of MEF3 and NFI proteins activates transcription in a subset of fast-twitch muscles.

1 reference

12 December 2020

Del(14)(q22.1q23.2) in a patient with anophthalmia and pituitary hypoplasia

1 reference

12 December 2020

Glucose stimulates translocation of the homeodomain transcription factor PDX1 from the cytoplasm to the nucleus in pancreatic beta-cells

1 reference

12 December 2020

Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site

1 reference

12 December 2020

Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophy

1 reference

12 December 2020

EYA4, a novel vertebrate gene related to Drosophila eyes absent

1 reference

12 December 2020

Expression of two myogenic regulatory factors myogenin and MyoDl during mouse embryogenesis

1 reference

12 December 2020

Pax3 is essential for skeletal myogenesis and the expression of Six1 and Eya2.

1 reference

12 December 2020

Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation

1 reference

12 December 2020

Mouse Eya genes are expressed during limb tendon development and encode a transcriptional activation function

1 reference

12 December 2020

Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human development

1 reference

12 December 2020

Eyeless initiates the expression of both sine oculis and eyes absent during Drosophila compound eye development.

1 reference

12 December 2020

sine oculis is a homeobox gene required for Drosophila visual system development

1 reference

12 December 2020

alpha11beta1 integrin is a receptor for interstitial collagens involved in cell migration and collagen reorganization on mesenchymal nonmuscle cells

1 reference

12 December 2020

Multiple roles of the eyes absent gene in Drosophila

1 reference

12 December 2020

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.

1 reference

12 December 2020

Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode

1 reference

12 December 2020