(Q29617873)

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11 November 2019

title

Systematic screen for human disease genes in yeast (English)

2 references

PubMed

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30 April 2017

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11 November 2019

1

1 reference

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11 November 2019

Dejana Mokranjac

4

1 reference

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11 November 2019

Holger Prokisch

9

1 reference

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11 November 2019

author name string

Curt Scharfe

2

1 reference

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11 November 2019

Adam M Deutschbauer

3

1 reference

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11 November 2019

Zelek S Herman

5

1 reference

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11 November 2019

Ted Jones

6

1 reference

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11 November 2019

Angela M Chu

7

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11 November 2019

Guri Giaever

8

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11 November 2019

Peter J Oefner

10

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11 November 2019

Ronald W Davis

11

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11 November 2019

language of work or name

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30 April 2017

publication date

22 July 2002

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11 November 2019

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11 November 2019

volume

31

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11 November 2019

issue

4

2 references

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11 November 2019

page(s)

400-404

1 reference

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Human genetic diseases: a cross-talk between man and yeast

11 November 2019

cites work

1 reference

7 January 2021

Nuclear power and mitochondrial disease

1 reference

7 January 2021

Mitochondrial diseases in man and mouse

1 reference

7 January 2021

Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis

1 reference

7 January 2021

A genome-wide screen in Saccharomyces cerevisiae for genes affecting UV radiation sensitivity

1 reference

7 January 2021

A DNA microarray-based genetic screen for nonhomologous end-joining mutants in Saccharomyces cerevisiae

1 reference

7 January 2021

Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar-coding strategy

1 reference

7 January 2021

Genetics of mitochondrial biogenesis

1 reference

7 January 2021

MITOP, the mitochondrial proteome database: 2000 update

1 reference

7 January 2021

Mitochondrial assembly in yeast.

1 reference

7 January 2021

A re-annotation of the Saccharomyces cerevisiae genome.

1 reference

7 January 2021

Computational method to predict mitochondrially imported proteins and their targeting sequences

1 reference

7 January 2021

The genome sequence of Rickettsia prowazekii and the origin of mitochondria

1 reference

7 January 2021

A network of protein-protein interactions in yeast

1 reference

7 January 2021

Subcellular localization of the yeast proteome

1 reference

7 January 2021

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

7 January 2021

Glucose depletion rapidly inhibits translation initiation in yeast

1 reference

7 January 2021

Exploring the metabolic and genetic control of gene expression on a genomic scale

1 reference

7 January 2021

Functional discovery via a compendium of expression profiles

1 reference

7 January 2021

ESTablishing a human transcript map

1 reference

7 January 2021

MIPS: a database for genomes and protein sequences

1 reference

7 January 2021

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

1 reference

7 January 2021

Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity.

1 reference

7 January 2021

Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.

1 reference

7 January 2021

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome

1 reference

7 January 2021

A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.

1 reference

7 January 2021

A novel X-linked dominant condition: X-linked congenital isolated ptosis

1 reference

7 January 2021

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Identifiers

2 references

30 April 2017

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Dimensions Publication ID

11 November 2019

1038368313

0 references

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2 references

30 April 2017