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Robert P Erickson

Showing results (81-90 of 113) with videos related to

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Gene Expression Patterns : GEP|October 7, 2004
Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndromeSusan L Dagenais, Rebecca L Hartsough, Robert P Erickson, et al.
Neuroscience Letters|October 7, 2008
Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish populationRobert P Erickson, Katherine Larson-Thomé, Lyndon Weberg, et al.
Gene|December 11, 2017
In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrinCraig A Marshall, Dawn E Watkins-Chow, Giampiero Palladino, et al.
Mitochondrion|December 22, 2019
Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1<sup>nmf164</sup>Robert P Erickson, Siddhesh Aras, Neeraja Purandare, et al.
Human Molecular Genetics|November 6, 2002
Rescue of neurodegeneration in Niemann-Pick C mice by a prion-promoter-driven Npc1 cDNA transgeneStacie K Loftus, Robert P Erickson, Steven U Walkley, et al.
Acta Neuropathologica Communications|September 3, 2016
Developmental delay in motor skill acquisition in Niemann-Pick C1 mice reveals abnormal cerebellar morphogenesisPaola Caporali, Francesco Bruno, Giampiero Palladino, et al.
Human Molecular Genetics|April 6, 2017
Shortened primary cilium length and dysregulated Sonic hedgehog signaling in Niemann-Pick C1 diseaseSonia Canterini, Jessica Dragotto, Andrea Dardis, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Athabascan brainstem dysgenesis syndromeSteve Holve, Barbara Friedman, H Eugene Hoyme, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 8, 2017
Pediatric Cytochrome P450 Activity Alterations in Nonalcoholic SteatohepatitisHui Li, Mark J Canet, John D Clarke, et al.
American Journal of Human Genetics|December 7, 2002
A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo populationZanhua Yi, Nanibaa' Garrison, Orit Cohen-Barak, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
Gene Expression Patterns : GEP|October 7, 2004
Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndromeSusan L Dagenais, Rebecca L Hartsough, Robert P Erickson, et al.
Neuroscience Letters|October 7, 2008
Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish populationRobert P Erickson, Katherine Larson-Thomé, Lyndon Weberg, et al.
Gene|December 11, 2017
In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrinCraig A Marshall, Dawn E Watkins-Chow, Giampiero Palladino, et al.
Mitochondrion|December 22, 2019
Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1<sup>nmf164</sup>Robert P Erickson, Siddhesh Aras, Neeraja Purandare, et al.
Human Molecular Genetics|November 6, 2002
Rescue of neurodegeneration in Niemann-Pick C mice by a prion-promoter-driven Npc1 cDNA transgeneStacie K Loftus, Robert P Erickson, Steven U Walkley, et al.
Acta Neuropathologica Communications|September 3, 2016
Developmental delay in motor skill acquisition in Niemann-Pick C1 mice reveals abnormal cerebellar morphogenesisPaola Caporali, Francesco Bruno, Giampiero Palladino, et al.
Human Molecular Genetics|April 6, 2017
Shortened primary cilium length and dysregulated Sonic hedgehog signaling in Niemann-Pick C1 diseaseSonia Canterini, Jessica Dragotto, Andrea Dardis, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Athabascan brainstem dysgenesis syndromeSteve Holve, Barbara Friedman, H Eugene Hoyme, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 8, 2017
Pediatric Cytochrome P450 Activity Alterations in Nonalcoholic SteatohepatitisHui Li, Mark J Canet, John D Clarke, et al.
American Journal of Human Genetics|December 7, 2002
A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo populationZanhua Yi, Nanibaa' Garrison, Orit Cohen-Barak, et al.
Pageof 12