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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Nature genetics, 2011-01, Vol.43 (1), p.23-26

2011

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Chronic kidney disease in type 2 diabetes: Implications for managing glycaemic control, cardiovascular and renal risk

Diabetes, obesity & metabolism, 2020-04, Vol.22 (S1), p.32-45

2020

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Beyond the Individual: Community‐Centric Approaches to Increase Diversity in Biomedical Research

Clinical pharmacology and therapeutics, 2023-03, Vol.113 (3), p.509-517

2023

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Different Roles for Tet1 and Tet2 Proteins in Reprogramming-Mediated Erasure of Imprints Induced by EGC Fusion

Molecular cell, 2013-03, Vol.49 (6), p.1023-1033

2013

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Active genes dynamically colocalize to shared sites of ongoing transcription

Nature genetics, 2004-10, Vol.36 (10), p.1065-1071

2004

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A high-resolution map of transcriptional repression

eLife, 2017-03, Vol.6

2017

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Jarid2 Coordinates Nanog Expression and PCP/Wnt Signaling Required for Efficient ESC Differentiation and Early Embryo Development

Cell reports (Cambridge), 2015-07, Vol.12 (4), p.573-586

2015

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Ensuring equity: Pharmacogenetic implementation in rural and tribal communities

Frontiers in pharmacology, 2022-09, Vol.13, p.953142-953142

2022

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Bioluminescence imaging of Cyp1a1-luciferase reporter mice demonstrates prolonged activation of the aryl hydrocarbon receptor in the lung

Communications biology, 2024-04, Vol.7 (1), p.442-442, Article 442

2024

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Reprogramming lineage identity through cell–cell fusion

Current opinion in genetics & development, 2021-10, Vol.70, p.15-23

2021

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Dynamic Repositioning of Genes in the Nucleus of Lymphocytes Preparing for Cell Division

Molecular cell, 1999-02, Vol.3 (2), p.207-217

1999

Volltextzugriff (PDF)

Diversity, Equity, and Inclusion: Translating Clinical Pharmacology for All

Clinical pharmacology and therapeutics, 2023-03, Vol.113 (3), p.457-461

2023

Volltextzugriff (PDF)

Keeping pace with CYP2D6 haplotype discovery: innovative methods to assign function

Pharmacogenomics, 2022-03, Vol.23 (4), p.255-262

2022

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A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation

Nature (London), 2011-08, Vol.476 (7361), p.467-471

2011

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Atypical heterochromatin organization and replication are rapidly acquired by somatic cells following fusion-mediated reprogramming by mouse ESCs

Cell cycle (Georgetown, Tex.), 2013-10, Vol.12 (20), p.3253-3261

2013

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Association of Transcriptionally Silent Genes with Ikaros Complexes at Centromeric Heterochromatin

Cell, 1997-12, Vol.91 (6), p.845-854

1997

Volltextzugriff (PDF)

Mutations in CDK5RAP2 cause Seckel syndrome

Molecular genetics & genomic medicine, 2015-09, Vol.3 (5), p.467-480

2015

Volltextzugriff (PDF)

Targeting of Ikaros to pericentromeric heterochromatin by direct DNA binding

Genes & development, 2000-09, Vol.14 (17), p.2146-2160

2000

Volltextzugriff (PDF)

Chromatin folding and gene expression: new tools to reveal the spatial organization of genes

Chromosome research, 2003-01, Vol.11 (5), p.423-433

Brown, Karen E

2003

Volltextzugriff (PDF)

Nonequivalent nuclear location of immunoglobulin alleles in B lymphocytes

Nature immunology, 2001-09, Vol.2 (9), p.848-854

2001

Volltextzugriff (PDF)

Women's contributions to visual culture, 1918-1939

Brown, Karen E

2008

Volltextzugriff (PDF)

Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells

Nature cell biology, 2001-06, Vol.3 (6), p.602-606

2001

Volltextzugriff (PDF)

Preschool boys with hearing loss are exposed to greater vocal amplitude from parents

The Journal of the Acoustical Society of America, 2020-10, Vol.148 (4), p.2469-2469

2020

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Heritable gene silencing in lymphocytes delays chromatid resolution without affecting the timing of DNA replication

Nature cell biology, 2003-07, Vol.5 (7), p.668-674

2003

Volltextzugriff (PDF)

Different Roles for Tet1 and Tet2 Proteins in Reprogramming-Mediated Erasure of Imprints Induced by EGC Fusion

Molecular cell, 2013-03, Vol.49 (6), p.1176-1176

2013

Volltextzugriff (PDF)

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Chronic kidney disease in type 2 diabetes: Implications for managing glycaemic control, cardiovascular and renal risk

Beyond the Individual: Community‐Centric Approaches to Increase Diversity in Biomedical Research

Different Roles for Tet1 and Tet2 Proteins in Reprogramming-Mediated Erasure of Imprints Induced by EGC Fusion

Active genes dynamically colocalize to shared sites of ongoing transcription

A high-resolution map of transcriptional repression

Jarid2 Coordinates Nanog Expression and PCP/Wnt Signaling Required for Efficient ESC Differentiation and Early Embryo Development

Ensuring equity: Pharmacogenetic implementation in rural and tribal communities

Bioluminescence imaging of Cyp1a1-luciferase reporter mice demonstrates prolonged activation of the aryl hydrocarbon receptor in the lung

Reprogramming lineage identity through cell–cell fusion

Dynamic Repositioning of Genes in the Nucleus of Lymphocytes Preparing for Cell Division

Diversity, Equity, and Inclusion: Translating Clinical Pharmacology for All

Keeping pace with CYP2D6 haplotype discovery: innovative methods to assign function

A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation

Atypical heterochromatin organization and replication are rapidly acquired by somatic cells following fusion-mediated reprogramming by mouse ESCs

Association of Transcriptionally Silent Genes with Ikaros Complexes at Centromeric Heterochromatin

Mutations in CDK5RAP2 cause Seckel syndrome

Targeting of Ikaros to pericentromeric heterochromatin by direct DNA binding

Chromatin folding and gene expression: new tools to reveal the spatial organization of genes

Nonequivalent nuclear location of immunoglobulin alleles in B lymphocytes

Women's contributions to visual culture, 1918-1939

Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells

Preschool boys with hearing loss are exposed to greater vocal amplitude from parents

Heritable gene silencing in lymphocytes delays chromatid resolution without affecting the timing of DNA replication

Different Roles for Tet1 and Tet2 Proteins in Reprogramming-Mediated Erasure of Imprints Induced by EGC Fusion

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