(Q28198386)

2

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J Fain

3

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E C Sener

4

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C J Selleck

5

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A H Awad

6

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J Zwaan

7

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P B Mullaney

8

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T M Bosley

9

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E C Engle

Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles.

10

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language of work or name

English

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publication date

November 2001

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published in

Nature Genetics

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volume

29

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issue

3

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page(s)

315-20

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cites work

1 reference

7 January 2021

Bilateral Duane's retraction syndrome. A clinical-pathologic case report

1 reference

7 January 2021

Unilateral Duane's retraction syndrome (Type 1).

1 reference

7 January 2021

Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.

1 reference

7 January 2021

A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.

1 reference

7 January 2021

Localization of a gene for Duane retraction syndrome to chromosome 2q31

1 reference

7 January 2021

Development of noradrenergic neurons in the zebrafish hindbrain requires BMP, FGF8, and the homeodomain protein soulless/Phox2a

1 reference

7 January 2021

The homeodomain protein Arix promotes protein kinase A-dependent activation of the dopamine beta-hydroxylase promoter through multiple elements and interaction with the coactivator cAMP-response element-binding protein-binding protein

1 reference

7 January 2021

Paired-like homeodomain proteins Phox2a/Arix and Phox2b/NBPhox have similar genetic organization and independently regulate dopamine beta-hydroxylase gene transcription

1 reference

7 January 2021

A homeodomain protein selectively expressed in noradrenergic tissue regulates transcription of neurotransmitter biosynthetic genes

1 reference

7 January 2021

Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a

1 reference

7 January 2021

Paired-like homeodomain proteins, Phox2a and Phox2b, are responsible for noradrenergic cell-specific transcription of the dopamine beta-hydroxylase gene

1 reference

7 January 2021

The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

1 reference

7 January 2021

Specification of the central noradrenergic phenotype by the homeobox gene Phox2b.

1 reference

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

7 January 2021

Statistical features of human exons and their flanking regions

1 reference

7 January 2021

Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences

1 reference

7 January 2021

Mutant WD-repeat protein in triple-A syndrome

1 reference

7 January 2021

The expression pattern of the transcription factor Phox2 delineates synaptic pathways of the autonomic nervous system

1 reference

7 January 2021

Dopamine beta-hydroxylase deficiency. A genetic disorder of cardiovascular regulation

1 reference

7 January 2021

A bacterial artificial chromosome library for sequencing the complete human genome

1 reference

7 January 2021