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TCF7L2 is a master regulator of insulin production and processing

Human molecular genetics, 2014-12, Vol.23 (24), p.6419-6431

2014

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Quantitative Dynamics of Chromatin Remodeling during Germ Cell Specification from Mouse Embryonic Stem Cells

Cell stem cell, 2015-05, Vol.16 (5), p.517-532

2015

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Case report: A novel R246L mutation in the LMX1B homeodomain causes isolated nephropathy in a large Chinese family

Medicine (Baltimore), 2024-03, Vol.103 (10), p.e37442-e37442

2024

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Transcriptome analysis of mouse and human sinoatrial node cells reveals a conserved genetic program

Development (Cambridge), 2019-01, Vol.146 (8)

2019

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Pioneer Factor NeuroD1 Rearranges Transcriptional and Epigenetic Profiles to Execute Microglia-Neuron Conversion

Neuron (Cambridge, Mass.), 2019-02, Vol.101 (3), p.472-485.e7

2019

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Generation of functional human serotonergic neurons from fibroblasts

Molecular psychiatry, 2016-01, Vol.21 (1), p.49-61

2016

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Single cell transcriptomics reveals lineage trajectory of retinal ganglion cells in wild-type and Atoh7-null retinas

Nature communications, 2021-03, Vol.12 (1), p.1465-1465, Article 1465

2021

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Myelodysplastic syndromes are induced by histone methylation–altering ASXL1 mutations

The Journal of clinical investigation, 2013-11, Vol.123 (11), p.4627-4640

2013

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Lhx6 Directly Regulates Arx and CXCR7 to Determine Cortical Interneuron Fate and Laminar Position

Neuron (Cambridge, Mass.), 2014-04, Vol.82 (2), p.350-364

2014

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Fibroblast growth factor 10 gene regulation in the second heart field by Tbx1, Nkx2-5, and Islet1 reveals a genetic switch for down-regulation in the myocardium

Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (45), p.18273-18280

2012

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LIM domain-binding 1 maintains the terminally differentiated state of pancreatic β cells

The Journal of clinical investigation, 2017-01, Vol.127 (1), p.215-229

2017

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Lhx2, an evolutionarily conserved, multifunctional regulator of forebrain development

Brain research, 2019-02, Vol.1705, p.1-14

2019

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LC3B is a cofactor for LMX1B-mediated transcription of autophagy genes in dopaminergic neurons

The Journal of cell biology, 2023-05, Vol.222 (5), p.1

2023

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Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma

The American journal of surgical pathology, 2020-05, Vol.44 (5), p.594

2020

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Accelerated high-yield generation of limb-innervating motor neurons from human stem cells

The Journal of neuroscience, 2013-01, Vol.33 (2), p.574-586

2013

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Development of the human female reproductive tract

Differentiation (London), 2018-09, Vol.103, p.46-65

2018

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Expression of regulatory genes in the embryonic brain of a lizard and implications for understanding pallial organization and evolution

Journal of comparative neurology (1911), 2018-01, Vol.526 (1), p.166-202

2018

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Direct Induction and Functional Maturation of Forebrain GABAergic Neurons from Human Pluripotent Stem Cells

Cell reports (Cambridge), 2016-08, Vol.16 (7), p.1942-1953

2016

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Role of Zeb2/Sip1 in neuronal development

Brain research, 2019-02, Vol.1705, p.24-31

2019

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LHX2 is necessary for the maintenance of optic identity and for the progression of optic morphogenesis

The Journal of neuroscience, 2013-04, Vol.33 (16), p.6877-6884

2013

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Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort

Clinical endocrinology (Oxford), 2015-12, Vol.83 (6), p.849-860

2015

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Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate

Neuron (Cambridge, Mass.), 2016-10, Vol.92 (1), p.59-74

2016

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Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

Clinical genetics, 2014-10, Vol.86 (4), p.326-334

2014

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Islet-1 Is essential for pancreatic β-cell function

Diabetes (New York, N.Y.), 2014-12, Vol.63 (12), p.4206-4217

2014

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Regulation of axial elongation by Cdx

Developmental biology, 2022-03, Vol.483, p.118-127

2022

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TCF7L2 is a master regulator of insulin production and processing

Quantitative Dynamics of Chromatin Remodeling during Germ Cell Specification from Mouse Embryonic Stem Cells

Case report: A novel R246L mutation in the LMX1B homeodomain causes isolated nephropathy in a large Chinese family

Transcriptome analysis of mouse and human sinoatrial node cells reveals a conserved genetic program

Pioneer Factor NeuroD1 Rearranges Transcriptional and Epigenetic Profiles to Execute Microglia-Neuron Conversion

Generation of functional human serotonergic neurons from fibroblasts

Single cell transcriptomics reveals lineage trajectory of retinal ganglion cells in wild-type and Atoh7-null retinas

Myelodysplastic syndromes are induced by histone methylation–altering ASXL1 mutations

Lhx6 Directly Regulates Arx and CXCR7 to Determine Cortical Interneuron Fate and Laminar Position

Fibroblast growth factor 10 gene regulation in the second heart field by Tbx1, Nkx2-5, and Islet1 reveals a genetic switch for down-regulation in the myocardium

LIM domain-binding 1 maintains the terminally differentiated state of pancreatic β cells

Lhx2, an evolutionarily conserved, multifunctional regulator of forebrain development

LC3B is a cofactor for LMX1B-mediated transcription of autophagy genes in dopaminergic neurons

Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma

Accelerated high-yield generation of limb-innervating motor neurons from human stem cells

Development of the human female reproductive tract

Expression of regulatory genes in the embryonic brain of a lizard and implications for understanding pallial organization and evolution

Direct Induction and Functional Maturation of Forebrain GABAergic Neurons from Human Pluripotent Stem Cells

Role of Zeb2/Sip1 in neuronal development

LHX2 is necessary for the maintenance of optic identity and for the progression of optic morphogenesis

Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort

Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

Islet-1 Is essential for pancreatic β-cell function

Regulation of axial elongation by Cdx

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