(Q28215649)

2

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M J Allen

3

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A Carey

4

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M Papaioannou

5

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C Chakarova

6

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M Al-Maghtheh

7

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N D Ebenezer

8

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C Willis

9

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A T Moore

10

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A C Bird

11

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D M Hunt

12

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S S Bhattacharya

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19

13

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language of work or name

English

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publication date

August 2001

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published in

Molecular Cell

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volume

8

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issue

2

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page(s)

375-81

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Segregation of a PRKCG mutation in two RP11 families

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

The Pfam protein families database.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Isolation of an essential Schizosaccharomyces pombe gene, prp31(+), that links splicing and meiosis

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Organization and expression of eucaryotic split genes coding for proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Sequence requirements for synthetic peptide-mediated translocation to the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Nucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Protein complement of rod outer segments of frog retina

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Circadian rhythm and light regulate opsin mRNA in rod photoreceptors

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

The structure and function of proteins involved in mammalian pre-mRNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

RP11 is the second most common locus for dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Circadian oscillation of photopigment transcript levels in the mouse retina.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

The PRP31 gene encodes a novel protein required for pre-mRNA splicing in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Prp31p promotes the association of the U4/U6 x U5 tri-snRNP with prespliceosomes to form spliceosomes in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Nop5p is a small nucleolar ribonucleoprotein component required for pre-18 S rRNA processing in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2801%2900305-7

7 January 2021