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Human microvasculature-on-a chip: anti-neovasculogenic effect of nintedanib in vitro

Angiogenesis (London), 2018-11, Vol.21 (4), p.861-871

2018

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Effects of biomechanical and biochemical stimuli on angio- and vasculogenesis in a complex microvasculature-on-chip

iScience, 2023-03, Vol.26 (3), p.106198-106198, Article 106198

2023

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Remodeling of an in vitro microvessel exposed to cyclic mechanical stretch

APL bioengineering, 2021-06, Vol.5 (2), p.026102-026102

2021

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Immune cell extravasation in an organ-on-chip to model lung inflammation

European journal of pharmaceutical sciences, 2023-08, Vol.187, p.106485-106485, Article 106485

2023

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Lung-on-a-Chip Models of the Lung Parenchyma

Advances in experimental medicine and biology, 2023, Vol.1413, p.191-211

2023

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Analysis of heat transfer and entropy generation for a low-Peclet-number microtube flow using a second-order slip model: an extended-Graetz problem

Journal of engineering mathematics, 2014-12, Vol.89 (1), p.13-25

2014

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Fabrication of continuous flow microfluidics device with 3D electrode structures for high throughput DEP applications using mechanical machining

Electrophoresis, 2015-07, Vol.36 (13), p.1432-1442

2015

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MP81-01 MICROVASCULATURE ON CHIP: CANCER CELLS EXTRAVASATION IN VITRO MODELING

The Journal of urology, 2019-04, Vol.201 (Supplement 4)

2019

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In vitro human lung microvasculature-on-chip: Anti-angiogenic efficacy of nintedanib

Toxicology letters, 2017-10, Vol.280, p.S276-S276

2017

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CD90 + CD146 + identifies a pulmonary mesenchymal cell subtype with both immune modulatory and perivascular-like function in postnatal human lung

American journal of physiology. Lung cellular and molecular physiology, 2020-04, Vol.318 (4), p.L813-L830

2020

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Microfluidic Device with 3d Electrode Structure for High Throughput Dielectrophoretic Applications

Zeinali, Soheila

2014

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Efficacy and antitumor activity of a mutant type of interleukin 2

Scientific reports, 2022-03, Vol.12 (1), p.5376-5376, Article 5376

2022

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Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility

Scientific reports, 2020-12, Vol.10 (1), p.21622-21622, Article 21622

2020

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Human IL-2Rɑ subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approach

PloS one, 2022, Vol.17 (2), p.e0264353-e0264353

2022

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Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

Human mutation, 2019-03, Vol.40 (3), p.288-298

2019

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Specific Targeting of Zinc Transporter LIV-1 with Immunocytokine Containing Anti-LIV-1 VHH and Human IL-2 and Evaluation of its In vitro Antitumor Activity

Current pharmaceutical design, 2024-01, Vol.30 (11), p.868

2024

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Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations

Journal of hepatology, 2019-08, Vol.71 (2), p.366-370

2019

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Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes

European journal of human genetics : EJHG, 2017-11, Vol.25 (11), p.1282-1285

2017

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Modeling aquifer hydrograph: performance review of conceptual MODFLOW and simulator models

Arabian journal of geosciences, 2020-03, Vol.13 (5), Article 240

2020

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Human IL-2R[alpha] subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approach

PloS one, 2022-02, Vol.17 (2), p.e0264353

2022

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Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

Human mutation, 2020-05, Vol.41 (5), p.906-912

2020

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Mutation update: The spectra of PLEC sequence variants and related plectinopathies

Human mutation, 2022-12, Vol.43 (12), p.1706-1731

2022

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Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages

Journal of investigative dermatology, 2017-03, Vol.137 (3), p.660-669

2017

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DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity

DNA repair, 2024-04, Vol.136, p.103633-103633, Article 103633

2024

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Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications

Journal of investigative dermatology, 2017-12, Vol.137 (12), p.2649-2652

2017

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Human microvasculature-on-a chip: anti-neovasculogenic effect of nintedanib in vitro

Effects of biomechanical and biochemical stimuli on angio- and vasculogenesis in a complex microvasculature-on-chip

Remodeling of an in vitro microvessel exposed to cyclic mechanical stretch

Immune cell extravasation in an organ-on-chip to model lung inflammation

Lung-on-a-Chip Models of the Lung Parenchyma

Analysis of heat transfer and entropy generation for a low-Peclet-number microtube flow using a second-order slip model: an extended-Graetz problem

Fabrication of continuous flow microfluidics device with 3D electrode structures for high throughput DEP applications using mechanical machining

MP81-01 MICROVASCULATURE ON CHIP: CANCER CELLS EXTRAVASATION IN VITRO MODELING

In vitro human lung microvasculature-on-chip: Anti-angiogenic efficacy of nintedanib

CD90 + CD146 + identifies a pulmonary mesenchymal cell subtype with both immune modulatory and perivascular-like function in postnatal human lung

Microfluidic Device with 3d Electrode Structure for High Throughput Dielectrophoretic Applications

Efficacy and antitumor activity of a mutant type of interleukin 2

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility

Human IL-2Rɑ subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approach

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

Specific Targeting of Zinc Transporter LIV-1 with Immunocytokine Containing Anti-LIV-1 VHH and Human IL-2 and Evaluation of its In vitro Antitumor Activity

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations

Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes

Modeling aquifer hydrograph: performance review of conceptual MODFLOW and simulator models

Human IL-2R[alpha] subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approach

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

Mutation update: The spectra of PLEC sequence variants and related plectinopathies

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages

DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications

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