Search Results - "Ljungberg, M Cecilia"
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Targeting AAV vectors to the central nervous system by engineering capsid-receptor interactions that enable crossing of the blood-brain barrier
Published in PLoS biology (19-07-2023)“…Viruses have evolved the ability to bind and enter cells through interactions with a wide variety of cell macromolecules. We engineered peptide-modified…”
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VCAM1 Is Induced in Ovarian Theca and Stromal Cells in a Mouse Model of Androgen Excess
Published in Endocrinology (Philadelphia) (01-06-2019)“…Abstract Ovarian theca androgen production is regulated by the pituitary LH and intrafollicular factors. Enhanced androgen biosynthesis by theca cells…”
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CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy
Published in Human molecular genetics (15-01-2012)“…Tauopathies, characterized by neurofibrillary tangles (NFTs) of phosphorylated tau proteins, are a group of neurodegenerative diseases, including…”
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Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome)
Published in PloS one (06-03-2012)“…Focal Dermal Hypoplasia (FDH) is a genetic disorder characterized by developmental defects in skin, skeleton and ectodermal appendages. FDH is caused by…”
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Rapamycin suppresses seizures and neuronal hypertrophy in a mouse model of cortical dysplasia
Published in Disease models & mechanisms (01-07-2009)“…Malformations of the cerebral cortex known as cortical dysplasia account for the majority of cases of intractable childhood epilepsy. With the exception of the…”
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Activation of mammalian target of rapamycin in cytomegalic neurons of human cortical dysplasia
Published in Annals of neurology (01-10-2006)“…Objective The cortex of patients with cortical dysplasia contains several abnormal cell types. Among the dysplastic cells, cytomegalic neurons are known to be…”
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Spatial distribution of marker gene activity in the mouse lung during alveolarization
Published in Data in brief (01-02-2019)“…This data is a curated collection of visual images of gene expression patterns from the pre- and post-natal mouse lung, accompanied by associated mRNA probe…”
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A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain
Published in Developmental cell (19-08-2024)“…Proneural transcription factors establish molecular cascades to orchestrate neuronal diversity. One such transcription factor, Atonal homolog 1 (Atoh1), gives…”
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A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins
Published in Brain research (18-06-2009)“…Abstract Very-low-density lipoprotein receptor (VLDLR) is a multi ligand apolipoprotein E (apoE) receptor and is involved in brain development through Reelin…”
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SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2
Published in Human molecular genetics (19-06-2023)“…Abstract SOX7 is a transcription factor-encoding gene located in a region on chromosome 8p23.1 that is recurrently deleted in individuals with ventricular…”
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An oocyte‐specific Cas9‐expressing mouse for germline CRISPR/Cas9‐mediated genome editing
Published in Genesis (New York, N.Y. : 2000) (01-04-2024)“…Summary Cas9 transgenes can be employed for genome editing in mouse zygotes. However, using transgenic instead of exogenous Cas9 to produce gene‐edited animals…”
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features
Published in American journal of human genetics (06-04-2017)“…Ubiquitination is a posttranslational modification that regulates many cellular processes including protein degradation, intracellular trafficking, cell…”
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Multifunctional Activity-Based Protein Profiling of the Developing Lung
Published in Journal of proteome research (03-08-2018)“…Lung diseases and disorders are a leading cause of death among infants. Many of these diseases and disorders are caused by premature birth and underdeveloped…”
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S100a4-Cre–mediated deletion of Ptch1 causes hypogonadotropic hypogonadism: role of pituitary hematopoietic cells in endocrine regulation
Published in JCI insight (25-07-2019)“…Hormones produced by the anterior pituitary gland regulate an array of important physiological functions, but the causes of pituitary hormone disorders are not…”
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Truncated apoE forms tangle-like structures in a neuronal cell line
Published in Neuroreport (07-05-2002)“…Apolipoprotein E is the predominant brain lipoprotein and polymorphic variation in the APOE gene the major genetic susceptibly factor for late onset…”
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Disruption of the ATXN1–CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans
Published in Nature genetics (01-04-2017)“…Huda Zoghbi and colleagues report that loss of the ATXN1–CIC protein complex in the developing mouse forebrain results in hyperactivity and defects in learning…”
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S100a4-Cre-mediated deletion of Patched1 causes hypogonadotropic hypogonadism: role of pituitary hematopoietic cells in endocrine regulation
Published in JCI insight (02-07-2019)“…Hormones produced by the anterior pituitary gland regulate an array of important physiological functions, but pituitary hormone disorders are not fully…”
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Monitoring the intracellular fate of apolipoprotein E: Implications for Alzheimer's disease
Published in Neurobiology of aging (01-05-2000)Get full text
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Survival of genetically engineered, adult-derived rat astrocytes grafted into the 6-hydroxydopamine lesioned adult rat striatum
Published in Brain research (16-01-1999)“…Astrocytes are potentially useful as vehicles for gene transfer into the CNS. As endogenous CNS cells, they possess secretory mechanisms and can be grown in…”
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