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Revisiting IL-2: Biology and therapeutic prospects

Science immunology, , Vol.3 (25)

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Generation of knock-in primary human T cells using Cas9 ribonucleoproteins

Proceedings of the National Academy of Sciences - PNAS, 2015-08, Vol.112 (33), p.10437-10442

2015

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Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements

Nature genetics, 2017-11, Vol.49 (11), p.1602-1612

2017

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DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics

Human mutation, 2013-06, Vol.34 (6), p.827-835

2013

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"T-bet"-ing on autoimmunity variants

PLoS genetics, 2017-09, Vol.13 (9), p.e1006924-e1006924

2017

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CRISPR screen in regulatory T cells reveals modulators of Foxp3

Nature (London), 2020-06, Vol.582 (7812), p.416-420

2020

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A large CRISPR-induced bystander mutation causes immune dysregulation

Communications biology, 2019-02, Vol.2 (1), p.70-70, Article 70

2019

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Functional CRISPR dissection of gene networks controlling human regulatory T cell identity

Nature immunology, 2020-11, Vol.21 (11), p.1456

2020

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Distinct Kinesin-14 mitotic mechanisms in spindle bipolarity

Cell cycle (Georgetown, Tex.), 2009-11, Vol.8 (21), p.3571-3583

2009

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Dysregulated RASGRP1 expression through RUNX1 mediated transcription promotes autoimmunity

European journal of immunology, 2021-02, Vol.51 (2), p.471-482

2021

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GRIN2A mutation and early‐onset epileptic encephalopathy: personalized therapy with memantine

Annals of clinical and translational neurology, 2014-03, Vol.1 (3), p.190-198

2014

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A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3)

Biochimica et biophysica acta, 2013-03, Vol.1833 (3), p.468-478

2013

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Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism

The Journal of clinical investigation, 2011-10, Vol.121 (10), p.3914-3923

2011

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VAR-MD: A tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance

Human mutation, 2012-04, Vol.33 (4), p.593-598

2012

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Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis

Neurology, 2012-07, Vol.79 (2), p.123

2012

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ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2892-2900

2014

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The Mechanical Properties of Drosophila Jump Muscle Expressing Wild-Type and Embryonic Myosin Isoforms

Biophysical journal, 2010-04, Vol.98 (7), p.1218-1226

2010

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Protein complexes at the microtubule organizing center regulate bipolar spindle assembly

Cell cycle (Georgetown, Tex.), 2008-05, Vol.7 (9), p.1246-1253

2008

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Cross-Species Analysis of Kinesin-14s: Human HSET Functions in Fission Yeast to Regulate Spindle Bipolarity

Biophysical journal, 2009-02, Vol.96 (3), p.571a-572a

2009

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Dissecting the genetic networks that control regulatory T cell stability using pooled CRISPR screens

The Journal of immunology (1950), 2018-05, Vol.200 (1_Supplement), p.101-101.5

2018

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A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching

Ophthalmic genetics, 2018-01, Vol.39 (1), p.41-45

2018

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A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching

Ophthalmic Genetics, 2018, Vol.39 (1), p.41-45

2018

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Revisiting IL-2: Biology and therapeutic prospects

Generation of knock-in primary human T cells using Cas9 ribonucleoproteins

Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements

DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics

"T-bet"-ing on autoimmunity variants

CRISPR screen in regulatory T cells reveals modulators of Foxp3

Discovery of stimulation-responsive immune enhancers with CRISPR activation

A large CRISPR-induced bystander mutation causes immune dysregulation

Functional CRISPR dissection of gene networks controlling human regulatory T cell identity

Distinct Kinesin-14 mitotic mechanisms in spindle bipolarity

Dysregulated RASGRP1 expression through RUNX1 mediated transcription promotes autoimmunity

GRIN2A mutation and early‐onset epileptic encephalopathy: personalized therapy with memantine

A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3)

Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism

VAR-MD: A tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance

Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis

Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation

ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

The Mechanical Properties of Drosophila Jump Muscle Expressing Wild-Type and Embryonic Myosin Isoforms

Protein complexes at the microtubule organizing center regulate bipolar spindle assembly

Cross-Species Analysis of Kinesin-14s: Human HSET Functions in Fission Yeast to Regulate Spindle Bipolarity

Dissecting the genetic networks that control regulatory T cell stability using pooled CRISPR screens

A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching

A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching

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