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High-Quality Binary Protein Interaction Map of the Yeast Interactome Network

Science (American Association for the Advancement of Science), 2008-10, Vol.322 (5898), p.104-110

2008

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Literature-curated protein interaction datasets

Nature methods, 2009-01, Vol.6 (1), p.39-46

2009

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tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans

PLoS genetics, 2013-10, Vol.9 (10), p.e1003888-e1003888

2013

Volltextzugriff (PDF)

Edgetic perturbation models of human inherited disorders

Molecular systems biology, 2009, Vol.5 (1), p.321-n/a

2009

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Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus

Journal of medical genetics, 2012-11, Vol.49 (11), p.708-712

2012

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Viral perturbations of host networks reflect disease etiology

PLoS computational biology, 2012-06, Vol.8 (6), p.e1002531-e1002531

2012

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Host-pathogen interactome mapping for HTLV-1 and -2 retroviruses

Retrovirology, 2012-03, Vol.9 (1), p.26-26, Article 26

2012

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Protein interactions of the transcription factor Hoxa1

BMC developmental biology, 2012-10, Vol.12 (1), p.29-29, Article 29

2012

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Confirmation of organized modularity in the yeast interactome

PLoS biology, 2007-06, Vol.5 (6), p.e153-e153

2007

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Proto―genes and de novo gene birth

Nature (London), 2012-07, Vol.487 (7407), p.370-374

2012

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An unusual presentation of de novo RAC3 variation in prenatal diagnosis

Child's nervous system, 2024-05, Vol.40 (5), p.1597-1602

2024

Volltextzugriff (PDF)

Modularity of the Transcriptional Response of Protein Complexes in Yeast

Journal of molecular biology, 2006-10, Vol.363 (2), p.589-610

2006

Volltextzugriff (PDF)

Revisiting the Saccharomyces cerevisiae predicted ORFeome

Genome Research, 2008-08, Vol.18 (8), p.1294-1303

2008

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Transcriptional regulation of protein complexes in yeast

Genome Biology, 2004-01, Vol.5 (5), p.R33-R33, Article R33

2004

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Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations

Neurology, 2014-05, Vol.82 (19), p.1749

2014

Volltextzugriff (PDF)

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

Journal of medical genetics, 2013-09, Vol.50 (9), p.585-592

2013

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The transcription factor ERG recruits CCR4-NOT to control mRNA decay and mitotic progression

Nature structural & molecular biology, 2016-07, Vol.23 (7), p.663

2016

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Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactor

BMC cancer, 2016-05, Vol.16 (334), p.335-335, Article 335

2016

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PP2A regulatory subunit Bα controls endothelial contractility and vessel lumen integrity via regulation of HDAC7

The EMBO journal, 2013-09, Vol.32 (18), p.2491-2503

2013

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MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43)

Neurology. Genetics, 2016-10, Vol.2 (5), p.e94-e94

2016

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Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia

Molecular biology of the cell, 2014-12, Vol.25 (24), p.3973-3985

2014

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Abstract 478: Predicting interactome networks perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.478-478

2014

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PP2A regulatory subunit B[alpha] controls endothelial contractility and vessel lumen integrity via regulation of HDAC7

The EMBO journal, 2013-09, Vol.32 (18), p.2491

2013

Volltextzugriff (PDF)

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High-Quality Binary Protein Interaction Map of the Yeast Interactome Network

Empirically controlled mapping of the Caenorhabditis elegans protein-protein interactome network

Literature-curated protein interaction datasets

tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans

Edgetic perturbation models of human inherited disorders

Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus

Viral perturbations of host networks reflect disease etiology

Host-pathogen interactome mapping for HTLV-1 and -2 retroviruses

Protein interactions of the transcription factor Hoxa1

Confirmation of organized modularity in the yeast interactome

Proto―genes and de novo gene birth

An unusual presentation of de novo RAC3 variation in prenatal diagnosis

Modularity of the Transcriptional Response of Protein Complexes in Yeast

Revisiting the Saccharomyces cerevisiae predicted ORFeome

Transcriptional regulation of protein complexes in yeast

An empirical framework for binary interactome mapping

Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

The transcription factor ERG recruits CCR4-NOT to control mRNA decay and mitotic progression

Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactor

PP2A regulatory subunit Bα controls endothelial contractility and vessel lumen integrity via regulation of HDAC7

MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43)

Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia

Abstract 478: Predicting interactome networks perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia

PP2A regulatory subunit B[alpha] controls endothelial contractility and vessel lumen integrity via regulation of HDAC7

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