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Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss

PloS one, 2012-11, Vol.7 (11), p.e50628-e50628

2012

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ASAH1 facilitates TNBC by DUSP5 suppression-driven activation of MAP kinase pathway and represents a therapeutic vulnerability

Cell death & disease, 2024-06, Vol.15 (6), p.452-17, Article 452

2024

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Comparative transcriptomics in human COPD reveals dysregulated genes uniquely expressed in ferrets

Respiratory research, 2022-10, Vol.23 (1), p.277-277, Article 277

2022

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Highly conserved non-coding sequences are associated with vertebrate development

PLoS biology, 2005-01, Vol.3 (1), p.e7-e7

2005

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Disruptor of telomeric silencing 1-like promotes ovarian cancer tumor growth by stimulating pro-tumorigenic metabolic pathways and blocking apoptosis

Oncogenesis (New York, NY), 2021-07, Vol.10 (7), p.48-48, Article 48

2021

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Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa

American journal of human genetics, 2011-02, Vol.88 (2), p.201-206

2011

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Challenges in whole exome sequencing: an example from hereditary deafness

PloS one, 2012-02, Vol.7 (2), p.e32000-e32000

2012

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Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach

PloS one, 2011-02, Vol.6 (2), p.e16917-e16917

2011

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Brown Fat AKT2 Is a Cold-Induced Kinase that Stimulates ChREBP-Mediated De Novo Lipogenesis to Optimize Fuel Storage and Thermogenesis

Cell metabolism, 2018-01, Vol.27 (1), p.195-209.e6

2018

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Comparison of three targeted enrichment strategies on the SOLiD sequencing platform

PloS one, 2011-04, Vol.6 (4), p.e18595-e18595

2011

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Ligand-activated BMP signaling inhibits cell differentiation and death to promote melanoma

The Journal of clinical investigation, 2018-01, Vol.128 (1), p.294-308

2018

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Human transcription factors responsive to initial reprogramming predominantly undergo legitimate reprogramming during fibroblast conversion to iPSCs

Scientific reports, 2020-11, Vol.10 (1), p.19710, Article 19710

2020

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Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

Annals of neurology, 2011-03, Vol.69 (3), p.464-470

2011

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The cJUN NH2-terminal kinase (JNK) pathway contributes to mouse mammary gland remodeling during involution

Cell death and differentiation, 2018-09, Vol.25 (9), p.1702-1715

2018

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Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

American journal of human genetics, 2012-11, Vol.91 (5), p.872-882

2012

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Changes in the Transcriptome and Chromatin Landscape in BRAFi-Resistant Melanoma Cells

Frontiers in oncology, 2022-06, Vol.12, p.937831-937831

2022

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Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes

Science (American Association for the Advancement of Science), 2002-08, Vol.297 (5585), p.1301-1310

2002

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Gld2-catalyzed 3' monoadenylation of miRNAs in the hippocampus has no detectable effect on their stability or on animal behavior

RNA (Cambridge), 2016-10, Vol.22 (10), p.1492-1499

2016

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Cholesterol-Independent SREBP-1 Maturation Is Linked to ARF1 Inactivation

Cell reports (Cambridge), 2016-06, Vol.16 (1), p.9-18

2016

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Divergent evolution of the myosin heavy chain gene family in fish and tetrapods: evidence from comparative genomic analysis

Physiological genomics, 2007-12, Vol.32 (1), p.1-15

2007

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Spt4 Promotes Pol I Processivity and Transcription Elongation

Genes, 2021-03, Vol.12 (3), p.413

2021

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A meta-analysis of microarray gene expression in mouse stem cells: redefining stemness

PloS one, 2008-07, Vol.3 (7), p.e2712-e2712

2008

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Defining the Influence of the A12.2 Subunit on Transcription Elongation and Termination by RNA Polymerase I In Vivo

Genes, 2021-11, Vol.12 (12), p.1939

2021

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CBX5 loss drives EGFR inhibitor resistance and results in therapeutically actionable vulnerabilities in lung cancer

Proceedings of the National Academy of Sciences - PNAS, 2023-01, Vol.120 (4), p.e2218118120-e2218118120

2023

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Insights into the regulation of intrinsically disordered proteins in the human proteome by analyzing sequence and gene expression data

Genome biology, 2009-01, Vol.10 (5), p.R50-R50

2009

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Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss

ASAH1 facilitates TNBC by DUSP5 suppression-driven activation of MAP kinase pathway and represents a therapeutic vulnerability

Comparative transcriptomics in human COPD reveals dysregulated genes uniquely expressed in ferrets

Highly conserved non-coding sequences are associated with vertebrate development

Disruptor of telomeric silencing 1-like promotes ovarian cancer tumor growth by stimulating pro-tumorigenic metabolic pathways and blocking apoptosis

Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa

Challenges in whole exome sequencing: an example from hereditary deafness

Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach

Brown Fat AKT2 Is a Cold-Induced Kinase that Stimulates ChREBP-Mediated De Novo Lipogenesis to Optimize Fuel Storage and Thermogenesis

Comparison of three targeted enrichment strategies on the SOLiD sequencing platform

Ligand-activated BMP signaling inhibits cell differentiation and death to promote melanoma

Human transcription factors responsive to initial reprogramming predominantly undergo legitimate reprogramming during fibroblast conversion to iPSCs

Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

The cJUN NH2-terminal kinase (JNK) pathway contributes to mouse mammary gland remodeling during involution

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Changes in the Transcriptome and Chromatin Landscape in BRAFi-Resistant Melanoma Cells

Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes

Gld2-catalyzed 3' monoadenylation of miRNAs in the hippocampus has no detectable effect on their stability or on animal behavior

Cholesterol-Independent SREBP-1 Maturation Is Linked to ARF1 Inactivation

Divergent evolution of the myosin heavy chain gene family in fish and tetrapods: evidence from comparative genomic analysis

Spt4 Promotes Pol I Processivity and Transcription Elongation

A meta-analysis of microarray gene expression in mouse stem cells: redefining stemness

Defining the Influence of the A12.2 Subunit on Transcription Elongation and Termination by RNA Polymerase I In Vivo

CBX5 loss drives EGFR inhibitor resistance and results in therapeutically actionable vulnerabilities in lung cancer

Insights into the regulation of intrinsically disordered proteins in the human proteome by analyzing sequence and gene expression data

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