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Temperature dependence of micelle shape transitions in copolymer solutions: the role of inter-block incompatibility

Soft matter, 2024-05, Vol.2 (17), p.3628-3634

2024

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ABC Triblock Copolymer Worms: Synthesis, Characterization, and Evaluation as Pickering Emulsifiers for Millimeter-Sized Droplets

Macromolecules, 2016-10, Vol.49 (20), p.7897-7907

2016

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Sulforaphane reduces hepatic glucose production and improves glucose control in patients with type 2 diabetes

Science translational medicine, 2017-06, Vol.9 (394)

2017

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Altered gene expression in slc4a11 -/- mouse cornea highlights SLC4A11 roles

Scientific reports, 2021-10, Vol.11 (1), p.20885-20885, Article 20885

2021

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Developing predictive molecular maps of human disease through community-based modeling

Nature genetics, 2012-02, Vol.44 (2), p.127-130

2012

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Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross

PloS one, 2010-12, Vol.5 (12), p.e14319-e14319

2010

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Vermicious thermo-responsive Pickering emulsifiers

Chemical science (Cambridge), 2015-07, Vol.6 (7), p.4207-4214

2015

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Sox5 regulates beta-cell phenotype and is reduced in type 2 diabetes

Nature communications, 2017-06, Vol.8 (1), p.15652-15652, Article 15652

2017

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Synthesis and pH-responsive dissociation of framboidal ABC triblock copolymer vesicles in aqueous solution

Chemical science (Cambridge), 2018-02, Vol.9 (6), p.1454-1463

2018

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Heterotelechelic homopolymers mimicking high χ - ultralow N block copolymers with sub-2 nm domain size

Chemical science (Cambridge), 2022-04, Vol.13 (14), p.4019-4028

2022

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The Wiskott-Aldrich Syndrome and X-Linked Congenital Thrombocytopenia Are Caused by Mutations of the Same Gene

Blood, 1995-11, Vol.86 (10), p.3797-3804

1995

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Interleukin 18 is a primary mediator of the inflammation associated with dextran sulphate sodium induced colitis: blocking interleukin 18 attenuates intestinal damage

Gut, 2002-06, Vol.50 (6), p.812-820

2002

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Polymer and Soft Matter Research at Diamond Light Source

Synchrotron radiation news, 2023-03, Vol.36 (2), p.37-45

2023

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Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters

Human molecular genetics, 1992-10, Vol.1 (7), p.505-510

1992

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Differential expression of DMD transcripts as a novel prognostic biomarker in histologically diverse mesotheliomas

Translational lung cancer research, 2024-04, Vol.13 (4), p.733-748

2024

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WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Human molecular genetics, 1995-07, Vol.4 (7), p.1127-1135

1995

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Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination

Blood, 2006-10, Vol.108 (7), p.2324-2331

2006

Volltextzugriff (PDF)

Integrative genomics and drug development

Pharmacogenomics, 2009-02, Vol.10 (2), p.203-212

2009

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Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. Cell . 1994. 78: 635-644

The Journal of immunology (1950), 2018-06, Vol.200 (11), p.3671-3680

2018

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Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins

Gene therapy, 2000-02, Vol.7 (4), p.314-320

2000

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Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge

Nature genetics, 2013-05, Vol.45 (5), p.468-469

2013

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Resolving candidate genes of mouse skeletal muscle QTL via RNA-Seq and expression network analyses

BMC genomics, 2012-11, Vol.13 (1), p.592-592

2012

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Gene expression elucidates functional impact of polygenic risk for schizophrenia

Nature neuroscience, 2016-11, Vol.19 (11), p.1442

2016

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RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain

Human molecular genetics, 1995-12, Vol.4 (12), p.2307-2311

1995

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Temperature dependence of micelle shape transitions in copolymer solutions: the role of inter-block incompatibility

ABC Triblock Copolymer Worms: Synthesis, Characterization, and Evaluation as Pickering Emulsifiers for Millimeter-Sized Droplets

Sulforaphane reduces hepatic glucose production and improves glucose control in patients with type 2 diabetes

Altered gene expression in slc4a11 -/- mouse cornea highlights SLC4A11 roles

Developing predictive molecular maps of human disease through community-based modeling

Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross

Vermicious thermo-responsive Pickering emulsifiers

Sox5 regulates beta-cell phenotype and is reduced in type 2 diabetes

Synthesis and pH-responsive dissociation of framboidal ABC triblock copolymer vesicles in aqueous solution

Heterotelechelic homopolymers mimicking high χ - ultralow N block copolymers with sub-2 nm domain size

The Wiskott-Aldrich Syndrome and X-Linked Congenital Thrombocytopenia Are Caused by Mutations of the Same Gene

Interleukin 18 is a primary mediator of the inflammation associated with dextran sulphate sodium induced colitis: blocking interleukin 18 attenuates intestinal damage

Polymer and Soft Matter Research at Diamond Light Source

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters

Early, precise, and safe clinical evaluation of the pharmacodynamic effects of novel agents in the intact human tumor microenvironment

Differential expression of DMD transcripts as a novel prognostic biomarker in histologically diverse mesotheliomas

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination

Integrative genomics and drug development

Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. Cell . 1994. 78: 635-644

Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins

Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge

Resolving candidate genes of mouse skeletal muscle QTL via RNA-Seq and expression network analyses

Gene expression elucidates functional impact of polygenic risk for schizophrenia

RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain

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