Search Results - "LANGE, JENNY"
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Pathomechanisms in the neuronal ceroid lipofuscinoses
Published in Biochimica et biophysica acta. Molecular basis of disease (01-09-2020)“…The neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative lysosomal storage disorders (LSDs), traditionally grouped together based…”
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Cerebral Organoids and Antisense Oligonucleotide Therapeutics: Challenges and Opportunities
Published in Frontiers in molecular neuroscience (27-06-2022)“…The advent of stem cell-derived cerebral organoids has already advanced our understanding of disease mechanisms in neurological diseases. Despite this, many…”
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Glial Dysfunction and Its Contribution to the Pathogenesis of the Neuronal Ceroid Lipofuscinoses
Published in Frontiers in neurology (04-04-2022)“…While significant efforts have been made in developing pre-clinical treatments for the neuronal ceroid lipofuscinoses (NCLs), many challenges still remain to…”
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Mislocalization of Nucleocytoplasmic Transport Proteins in Human Huntington's Disease PSC-Derived Striatal Neurons
Published in Frontiers in cellular neuroscience (29-09-2021)“…Huntington's disease (HD) is an inherited neurodegenerative disorder caused by a CAG repeat expansion in the huntingtin gene ( ). Disease progression is…”
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Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Published in Acta neuropathologica communications (08-08-2018)“…The neuronal ceroid lipofuscinoses (NCLs) are the most common cause of childhood dementia and are invariably fatal. Early localized glial activation occurs in…”
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PolyQ length-dependent metabolic alterations and DNA damage drive human astrocyte dysfunction in Huntington’s disease
Published in Progress in neurobiology (01-06-2023)“…Huntington’s Disease (HD) is a neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the Huntingtin gene. Astrocyte dysfunction is known to…”
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Cover Image, Volume 70, Issue 3
Published in Glia (01-03-2022)“…Cover Illustration: Dystrophin, a protein mutated in Duchenne muscular dystrophy, is expressed in human astrocytes differentiated from neural stem cells and…”
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Dystrophin deficiency affects human astrocyte properties and response to damage
Published in Glia (01-03-2022)“…In addition to progressive muscular degeneration due to dystrophin mutations, 1/3 of Duchenne muscular dystrophy (DMD) patients present cognitive deficits…”
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Identification of rare non-synonymous variants in SYNE1/CPG2 in bipolar affective disorder
Published in Psychiatric genetics (01-06-2017)“…Bipolar affective disorder (BPD) is a severe mood disorder with a prevalence of ˜1.5% in the population. The pathogenesis of BPD is poorly understood; however,…”
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The glial contribution to pathogenesis differs between forms of Batten disease: implications for therapy
Published in Molecular genetics and metabolism (01-01-2017)Get full text
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Neuron-glia interactions in infantile neuronal ceroid lipofuscinosis (cln1 disease)
Published 01-01-2016“…The neuronal ceroid lipofuscinoses (NCLs) are the most common cause of childhood dementia and are invariably fatal. Early, localised glial activation occurs in…”
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Dissertation -
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Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder
Published in Psychiatric genetics (01-06-2017)“…BACKGROUNDBipolar affective disorder (BPD) is a severe mood disorder with a prevalence of ∼1.5% in the population. The pathogenesis of BPD is poorly…”
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Journal Article -
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The Effects of Measures of Language Experience and Language Ability on Segmental Accuracy in Bilingual Children
Published in American journal of speech-language pathology (01-08-2010)“…Purpose: The present study investigated the effects of selected measures of language experience (parent-reported estimates of frequency of output and language…”
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Collaborative Investigation of Inclusive Early Education Practices
Published in Journal of early intervention (01-07-1999)“…This paper describes the rationale, development, and first-year implementation of Wisconsin's Preschool Action Research and Development Initiative (PARDI)…”
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Collaborative Investigation of Inclusive Early Education Practices: A Blueprint for Teacher-Researcher Partnership
Published in Journal of early intervention (01-07-1999)“…This paper describes the rationale, development, and first-year implementation of Wisconsin's Preschool Action Research and Development Initiative (PARDI)…”
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Out of the Nest: Instructional Strategies to Prepare Young, Exceptional Children for the Mainstream
Published 01-10-1979“…Designed to help prepare handicapped preschool children for mainstreaming, the manual describes 37 skills and related strategies for teaching those skills. The…”
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