Publications by authors named "Jacob Loupe"

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Allele-specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs.
Ashlyn G Anderson, Belle A Moyers, Jacob M Loupe, Ivan Rodriguez-Nunez, Stephanie A Felker

Genome Res· September 2024

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Multiomic profiling of transcription factor binding and function in human brain.
Jacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, Ivan Rodriguez-Nunez, Belle Moyers

Nat Neurosci· July 2024

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Base editing strategies to convert CAG to CAA diminish the disease-causing mutation in Huntington's disease.
Doo Eun Choi, Jun Wan Shin, Sophia Zeng, Eun Pyo Hong, Jae-Hyun Jang, Jacob M Loupe

Elife· June 2024

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Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs.
Belle A Moyers, Jacob M Loupe, Stephanie A Felker, James M J Lawlor, Ashlyn G Anderson

bioRxiv· October 2023

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Base editing strategies to convert CAG to CAA diminish the disease-causing mutation in Huntington's disease.
Doo Eun Choi, Jun Wan Shin, Sophia Zeng, Eun Pyo Hong, Jae-Hyun Jang, Jacob M Loupe

bioRxiv· April 2023

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Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer's disease-specific -regulatory elements.
Ashlyn G Anderson, Brianne B Rogers, Jacob M Loupe, Ivan Rodriguez-Nunez, Sydney C Roberts

Cell Genom· March 2023

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Huntingtin turnover: modulation of huntingtin degradation by cAMP-dependent protein kinase A (PKA) phosphorylation of C-HEAT domain Ser2550.
Yejin Lee, Hyeongju Kim, Douglas Barker, Ravi Vijayvargia, Ranjit Singh Atwal, Jacob Loupe

Hum Mol Genet· January 2023

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Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs.
Roy Jung, Yejin Lee, Douglas Barker, Kevin Correia, Baehyun Shin, Jacob Loupe

Hum Mol Genet· April 2021

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Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
Jacob M Loupe, Ricardo Mouro Pinto, Kyung-Hee Kim, Tammy Gillis, Jayalakshmi S Mysore

Hum Mol Genet· November 2020

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Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.
Kyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, Michael J Chao, Jacob Loupe

Am J Hum Genet· July 2020

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Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease.
Natalie Ellis, Amelia Tee, Branduff McAllister, Thomas Massey, Duncan McLauchlan, Jacob Loupe

Biol Psychiatry· May 2020

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Acquisition of an oncogenic fusion protein is sufficient to globally alter the landscape of miRNA expression to inhibit myogenic differentiation.
Jacob M Loupe, Patrick J Miller, Judy S Crabtree, Jovanny Zabaleta, Andrew D Hollenbach

Oncotarget· October 2017

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Acquisition of an oncogenic fusion protein serves as an initial driving mutation by inducing aneuploidy and overriding proliferative defects.
Jacob M Loupe, Patrick J Miller, Benjamin P Bonner, Elaine C Maggi, Jyothi Vijayaraghavan

Oncotarget· September 2016

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Familial co-segregation of Coffin-Lowry syndrome inherited from the mother and autosomal dominant Waardenburg type IV syndrome due to deletion of EDNRB inherited from the father.
Jacob Loupe, Srirangan Sampath, Yves Lacassie

Eur J Med Genet· October 2014

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Phosphorylation of PAX3 contributes to melanoma phenotypes by affecting proliferation, invasion, and transformation.
Aditi S Iyengar, Patrick J Miller, Jacob M Loupe, Andrew D Hollenbach

Pigment Cell Melanoma Res· September 2014

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Identification of CK2 as the kinase that phosphorylates Pax3 at Ser209 in early myogenic differentiation.
Aditi S Iyengar, Jacob M Loupe, Patrick J Miller, Andrew D Hollenbach

Biochem Biophys Res Commun· November 2012

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Identification of serines 201 and 209 as sites of Pax3 phosphorylation and the altered phosphorylation status of Pax3-FOXO1 during early myogenic differentiation.
Kevin N Dietz, Patrick J Miller, Aditi S Iyengar, Jacob M Loupe, Andrew D Hollenbach

Int J Biochem Cell Biol· June 2011

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