Philip H. Schwartz

Isolation and characterization of neural progenitor cells from post-mortem human cortex.

Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element.

Asymmetric localization of LGN but not AGS3, two homologs of Drosophila pins, in dividing human neural progenitor cells.

Isolation of retinal progenitor cells from post-mortem human tissue and comparison with autologous brain progenitors.

Neural progenitor cells from an adult patient with fragile X syndrome.

Human neural stem cell growth and differentiation in a gradient-generating microfluidic device.

Expression of neurodevelopmental markers by cultured porcine neural precursor cells.

Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.

The potential of stem cell therapies for neurological diseases.

Regulation of human neural precursor cells by laminin and integrins.

Mammalian stem cells.

An approach to the ethical donation of human embryos for harvest of stem cells.

Oxygen tension controls the expansion of human CNS precursors and the generation of astrocytes and oligodendrocytes.

Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic cat.

Differentiation of neural lineage cells from human pluripotent stem cells.

Invasion suppressor cystatin E/M (CST6): high-level cell type-specific expression in normal brain and epigenetic silencing in gliomas.

Neonatal neural progenitor cells and their neuronal and glial cell derivatives are fully permissive for human cytomegalovirus infection.

Regulatory networks define phenotypic classes of human stem cell lines.

Isolation of progenitor cells from GFP-transgenic pigs and transplantation to the retina of allorecipients.

Hypoxia and HIF1alpha repress the differentiative effects of BMPs in high-grade glioma.

Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II.

A novel DNMT3B splice variant expressed in tumor and pluripotent cells modulates genomic DNA methylation patterns and displays altered DNA binding.

Human cytomegalovirus infection causes premature and abnormal differentiation of human neural progenitor cells.

Neural stem/progenitors and glioma stem-like cells have differential sensitivity to chemotherapy.

The distinction between parthenotes and embryos is not easily made.

Xenotransplantation of human neural progenitor cells to the subretinal space of nonimmunosuppressed pigs.

The stem cell laboratory: design, equipment, and oversight.

Derivation of induced pluripotent stem cells by lentiviral transduction.

Traditional human embryonic stem cell culture.

Adaptation of human pluripotent stem cells to feeder-free conditions in chemically defined medium with enzymatic single-cell passaging.

Immunocytochemical analysis of human pluripotent stem cells.

The generation of embryoid bodies from feeder-based or feeder-free human pluripotent stem cell cultures.

Noninvasive diagnosis of mucopolysaccharidosis via depth-resolved optical spectroscopy of the outer ear.

Neural stem/progenitors and glioma stem-like cells have differential sensitivity to chemotherapy.

A faster immunofluorescence assay for tracking infection progress of human cytomegalovirus.

Viral mitochondria-localized inhibitor of apoptosis (UL37 exon 1 protein) does not protect human neural precursor cells from human cytomegalovirus-induced cell death.

Cancer stem cells from a rare form of glioblastoma multiforme involving the neurogenic ventricular wall.

Process-based expansion and neural differentiation of human pluripotent stem cells for transplantation and disease modeling.

Later passages of neural progenitor cells from neonatal brain are more permissive for human cytomegalovirus infection.

Identification of fragile X syndrome specific molecular markers in human fibroblasts: a useful model to test the efficacy of therapeutic drugs.

The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery.

A novel, long-lived, and highly engraftable immunodeficient mouse model of mucopolysaccharidosis type I.

The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery.

Immune-Mediated Inflammation May Contribute to the Pathogenesis of Cardiovascular Disease in Mucopolysaccharidosis Type I.