(Q47070337)

4 January 2018

title

dfh is a Drosophila homolog of the Friedreich's ataxia disease gene (English)

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4 January 2018

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5

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María D. Moltó

object named as

Moltó MD

6

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author name string

Cañizares J

1

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4 January 2018

Blanca JM

2

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4 January 2018

Navarro JA

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4 January 2018

Monrós E

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4 January 2018

language of work or name

English

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publication date

1 October 2000

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4 January 2018

published in

Gene

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4 January 2018

volume

256

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4 January 2018

issue

1-2

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4 January 2018

page(s)

35-42

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4 January 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

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Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

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Identification of nuclear genes encoding mitochondrial proteins: isolation of a collection of D. melanogaster cDNAs homologous to sequences in the Human Gene Index database

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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7 January 2021

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

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Analysis of membrane and surface protein sequences with the hydrophobic moment plot

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7 January 2021

Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria

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Cleavage-site motifs in mitochondrial targeting peptides

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Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction

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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

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Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

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Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

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Friedreich's ataxia: an epidemiological study in Valencia, Spain, based on consanguinity analysis

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Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat

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A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene

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Receptor tyrosine kinases: genetic evidence for their role in Drosophila and mouse development

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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7 January 2021

Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

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7 January 2021

Intrafamilial correlation in Friedreich's ataxia

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7 January 2021

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7 January 2021

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Identifiers

DOI

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4 January 2018

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4 January 2018