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Concise Review: Reactive Astrocytes and Stem Cells in Spinal Cord Injury: Good Guys or Bad Guys?

Stem cells (Dayton, Ohio), 2015-04, Vol.33 (4), p.1036-1041

2015

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Concise Review: Human Induced Pluripotent Stem Cell Models of Retinitis Pigmentosa

Stem cells (Dayton, Ohio), 2018-04, Vol.36 (4), p.474-481

2018

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Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1

Scientific reports, 2020-03, Vol.10 (1), p.5426-5426, Article 5426

2020

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Pluripotent stem cell regulation in Spain and the Spanish National Stem Cell Bank

Stem cell research, 2020-10, Vol.48, p.101956-101956, Article 101956

2020

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Perspectives and future directions of human pluripotent stem cell-based therapies: lessons from Geron's clinical trial for spinal cord injury

Stem cells and development, 2014-01, Vol.23 (1), p.1

2014

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Complete rat spinal cord transection as a faithful model of spinal cord injury for translational cell transplantation

Scientific reports, 2015-04, Vol.5 (1), p.9640-9640, Article 9640

2015

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Concise Review: Human Pluripotent Stem Cells in the Treatment of Spinal Cord Injury

Stem cells (Dayton, Ohio), 2012-09, Vol.30 (9), p.1787-1792

2012

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Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells

Frontiers in neuroscience, 2021-04, Vol.15, p.636969

2021

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Human iPSC derived disease model of MERTK-associated retinitis pigmentosa

Scientific reports, 2015-08, Vol.5 (1), p.12910-12910, Article 12910

2015

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Brief Report: Astrogliosis Promotes Functional Recovery of Completely Transected Spinal Cord Following Transplantation of hESC‐Derived Oligodendrocyte and Motoneuron Progenitors

Stem cells (Dayton, Ohio), 2014-02, Vol.32 (2), p.594-599

2014

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Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs5 mutation in MERTK

Stem cell research, 2019-01, Vol.34, p.101341-101341, Article 101341

2019

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Generation of a human iPSC line by mRNA reprogramming

Stem cell research, 2018-04, Vol.28, p.157-160

2018

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Synthetic pulmonary surfactant preparations: new developments and future trends

Current medicinal chemistry, 2008-02, Vol.15 (4), p.393

2008

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Generation of an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling

Stem cell research, 2019-07, Vol.38, p.101455-101455, Article 101455

2019

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Highly Efficient Neural Conversion of Human Pluripotent Stem Cells in Adherent and Animal‐Free Conditions

Stem cells translational medicine, 2017-04, Vol.6 (4), p.1217-1226

2017

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Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1

Stem cell research, 2018-12, Vol.33, p.151-155

2018

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Interfacial Behavior of Recombinant Forms of Human Pulmonary Surfactant Protein SP-C

Langmuir, 2012-05, Vol.28 (20), p.7811-7825

2012

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Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene

Stem cell research, 2017-05, Vol.21 (C), p.23-25

2017

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Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

Stem cell research, 2018-04, Vol.28, p.96-99

2018

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Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal

Molecular vision, 2019, Vol.25, p.663-678

2019

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Generation and characterization of human USH2A retinal disease model

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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hiPSC Disease Modeling of Rare Hereditary Cerebellar Ataxias: Opportunities and Future Challenges

The Neuroscientist (Baltimore, Md.), 2017-10, Vol.23 (5), p.554-566

2017

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Unraveling the Developmental Roadmap toward Human Brown Adipose Tissue

Stem cell reports, 2021-03, Vol.16 (3), p.641-655

2021

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Corrigendum to Generation of a human iPSC line by mRNA reprogramming. Stem Cell Res., Volume 28, April 2018, Pages 157–160

Stem cell research, 2018-08, Vol.31, p.51-51

2018

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Unraveling the Developmental Roadmap toward Human Brown AdiposeTissue

Stem cell reports, 2021-04, Vol.16 (4), p.1010-1010

2021

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Concise Review: Reactive Astrocytes and Stem Cells in Spinal Cord Injury: Good Guys or Bad Guys?

Concise Review: Human Induced Pluripotent Stem Cell Models of Retinitis Pigmentosa

Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1

Pluripotent stem cell regulation in Spain and the Spanish National Stem Cell Bank

Perspectives and future directions of human pluripotent stem cell-based therapies: lessons from Geron's clinical trial for spinal cord injury

Complete rat spinal cord transection as a faithful model of spinal cord injury for translational cell transplantation

Concise Review: Human Pluripotent Stem Cells in the Treatment of Spinal Cord Injury

Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells

Human iPSC derived disease model of MERTK-associated retinitis pigmentosa

Brief Report: Astrogliosis Promotes Functional Recovery of Completely Transected Spinal Cord Following Transplantation of hESC‐Derived Oligodendrocyte and Motoneuron Progenitors

Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs5 mutation in MERTK

Generation of a human iPSC line by mRNA reprogramming

Synthetic pulmonary surfactant preparations: new developments and future trends

Generation of an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling

Highly Efficient Neural Conversion of Human Pluripotent Stem Cells in Adherent and Animal‐Free Conditions

Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1

Interfacial Behavior of Recombinant Forms of Human Pulmonary Surfactant Protein SP-C

Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene

Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal

Generation and characterization of human USH2A retinal disease model

hiPSC Disease Modeling of Rare Hereditary Cerebellar Ataxias: Opportunities and Future Challenges

Unraveling the Developmental Roadmap toward Human Brown Adipose Tissue

Corrigendum to Generation of a human iPSC line by mRNA reprogramming. Stem Cell Res., Volume 28, April 2018, Pages 157–160

Unraveling the Developmental Roadmap toward Human Brown AdiposeTissue

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