Search Results - "Bergren, Sarah K."
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Single luminal epithelial progenitors can generate prostate organoids in culture
Published in Nature cell biology (01-10-2014)“…The intrinsic ability to exhibit self-organizing morphogenetic properties in ex vivo culture may represent a general property of tissue stem cells. Here we…”
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2
Tumor Evolution and Drug Response in Patient-Derived Organoid Models of Bladder Cancer
Published in Cell (05-04-2018)“…Bladder cancer is the fifth most prevalent cancer in the U.S., yet is understudied, and few laboratory models exist that reflect the biology of the human…”
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3
Luminal Cells Are Favored as the Cell of Origin for Prostate Cancer
Published in Cell reports (Cambridge) (11-09-2014)“…The identification of cell types of origin for cancer has important implications for tumor stratification and personalized treatment. For prostate cancer, the…”
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4
A computational systems approach identifies synergistic specification genes that facilitate lineage conversion to prostate tissue
Published in Nature communications (21-04-2017)“…To date, reprogramming strategies for generating cell types of interest have been facilitated by detailed understanding of relevant developmental regulatory…”
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Differential requirements of androgen receptor in luminal progenitors during prostate regeneration and tumor initiation
Published in eLife (15-01-2018)“…Master regulatory genes of tissue specification play key roles in stem/progenitor cells and are often important in cancer. In the prostate, androgen receptor…”
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6
Lineage analysis of basal epithelial cells reveals their unexpected plasticity and supports a cell-of-origin model for prostate cancer heterogeneity
Published in Nature cell biology (01-03-2013)“…A key issue in cancer biology is whether oncogenic transformation of different cell types of origin within an adult tissue gives rise to distinct tumour…”
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CRISPR/Cas9-Mediated Point Mutation in Nkx3.1 Prolongs Protein Half-Life and Reverses Effects Nkx3.1 Allelic Loss
Published in Cancer research (Chicago, Ill.) (01-11-2020)“…is the most commonly deleted gene in prostate cancer and is a gatekeeper suppressor. is haploinsufficient, and pathogenic reduction in protein levels may…”
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Nestin+NG2+ Cells Form a Reserve Stem Cell Population in the Mouse Prostate
Published in Stem cell reports (11-06-2019)“…In the prostate, stem and progenitor cell regenerative capacities have been ascribed to both basal and luminal epithelial cells. Here, we show that a rare…”
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Deleterious Variants of FIG4, a Phosphoinositide Phosphatase, in Patients with ALS
Published in American journal of human genetics (09-01-2009)“…Mutations of the lipid phosphatase FIG4 that regulates PI(3,5)P2 are responsible for the recessive peripheral-nerve disorder CMT4J. We now describe…”
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10
Fine mapping of an epilepsy modifier gene on mouse Chromosome 19
Published in Mammalian genome (01-06-2009)“…Mutations in voltage-gated sodium channels are associated with several types of human epilepsy. Variable expressivity and penetrance are common features of…”
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Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a
Published in Mammalian genome (01-09-2005)“…Mutations in the voltage-gated sodium channels SCN 1 A and SCN 2 A are responsible for several types of human epilepsy. Variable expressivity among family…”
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Evidence for a direct role of the disease modifier SCNM1 in splicing
Published in Human molecular genetics (15-10-2007)“…We originally isolated Scnm1 as a disease modifier gene that is required for efficient in vivo splicing of a mutant splice donor site in the sodium channel…”
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Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2
Published in Human molecular genetics (15-03-2006)“…A mutation in the voltage-gated sodium-channel Scn2a results in moderate epilepsy in transgenic Scn2aQ54 mice maintained on a C57BL/6J strain background. The…”
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14
Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channelScn2a
Published in Mammalian genome (01-09-2005)“…Mutations in the voltage-gated sodium channels SCN1A and SCN2A are responsible for several types of human epilepsy. Variable expressivity among family members…”
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