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Robert P Erickson

Showing results (71-80 of 113) with videos related to

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Gene|October 25, 2011
Genetic variation in the mouse model of Niemann Pick C1 affects female, as well as male, adiposity, and hepatic bile transporters but has indeterminate effects on caveolaeDavid A Jelinek, Bita Maghsoodi, Ivan A Borbon, et al.
Molecular Genetics and Metabolism|April 5, 2011
Pulmonary function and pathology in hydroxypropyl-beta-cyclodextin-treated and untreated Npc1⁻/⁻ miceAkshay Muralidhar, Ivan A Borbon, Dyadin M Esharif, et al.
Biorxiv : the Preprint Server for Biology|August 20, 2025
Manual lymph drainage massage of the head and neck improves cognition and reduces pathological biomarkers in the <i>5x-FAD</i> mouse model of Alzheimers diseaseMitchell J Bartlett, Robert P Erickson, Jennifer Frye, et al.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patientsLisa L Wang, Anu Gannavarapu, Carol L Clericuzio, et al.
Journal of Magnetic Resonance Imaging : JMRI|November 3, 2011
In vivo assessment of neurodegeneration in Niemann-Pick type C mice by quantitative T2 mapping and diffusion tensor imagingJohn W Totenhagen, Silvia Lope-Piedrafita, Ivan A Borbon, et al.
Orphanet Journal of Rare Diseases|October 14, 2015
Visual evoked potentials of Niemann-Pick type C1 mice reveal an impairment of the visual pathway that is rescued by 2-hydroxypropyl-ß-cyclodextrinGiampiero Palladino, Stefano Loizzo, Andrea Fortuna, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generationCarole Sargent, Julien Bauer, Muhamed Khalil, et al.
Clinical Genetics|August 13, 2019
Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second familyRobert P Erickson, Li-Wen Lai, Debbie J Mustacich, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del maleRobert P Erickson, Steve Skinner, Hélène Jacquet, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
Gene|October 25, 2011
Genetic variation in the mouse model of Niemann Pick C1 affects female, as well as male, adiposity, and hepatic bile transporters but has indeterminate effects on caveolaeDavid A Jelinek, Bita Maghsoodi, Ivan A Borbon, et al.
Molecular Genetics and Metabolism|April 5, 2011
Pulmonary function and pathology in hydroxypropyl-beta-cyclodextin-treated and untreated Npc1⁻/⁻ miceAkshay Muralidhar, Ivan A Borbon, Dyadin M Esharif, et al.
Biorxiv : the Preprint Server for Biology|August 20, 2025
Manual lymph drainage massage of the head and neck improves cognition and reduces pathological biomarkers in the <i>5x-FAD</i> mouse model of Alzheimers diseaseMitchell J Bartlett, Robert P Erickson, Jennifer Frye, et al.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patientsLisa L Wang, Anu Gannavarapu, Carol L Clericuzio, et al.
Journal of Magnetic Resonance Imaging : JMRI|November 3, 2011
In vivo assessment of neurodegeneration in Niemann-Pick type C mice by quantitative T2 mapping and diffusion tensor imagingJohn W Totenhagen, Silvia Lope-Piedrafita, Ivan A Borbon, et al.
Orphanet Journal of Rare Diseases|October 14, 2015
Visual evoked potentials of Niemann-Pick type C1 mice reveal an impairment of the visual pathway that is rescued by 2-hydroxypropyl-ß-cyclodextrinGiampiero Palladino, Stefano Loizzo, Andrea Fortuna, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generationCarole Sargent, Julien Bauer, Muhamed Khalil, et al.
Clinical Genetics|August 13, 2019
Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second familyRobert P Erickson, Li-Wen Lai, Debbie J Mustacich, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del maleRobert P Erickson, Steve Skinner, Hélène Jacquet, et al.
Pageof 12