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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 caveolae
David 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⁻/⁻ mice
Akshay 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 disease
Mitchell J Bartlett, Robert P Erickson, Jennifer Frye, et al.
Nature Reviews. Disease Primers
|
October 22, 2021
Primary lymphoedema
Pascal 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 patients
Lisa 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 imaging
John 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-cyclodextrin
Giampiero 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 generation
Carole Sargent, Julien Bauer, Muhamed Khalil, et al.
Clinical Genetics
|
August 13, 2019
Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family
Robert 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 male
Robert P Erickson, Steve Skinner, Hélène Jacquet, et al.
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of 12
Search research articles
Search
Showing results (71-80 of 113) with videos related to
Sort By:
Page
of 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 caveolae
David 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⁻/⁻ mice
Akshay 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 disease
Mitchell J Bartlett, Robert P Erickson, Jennifer Frye, et al.
Nature Reviews. Disease Primers
|
October 22, 2021
Primary lymphoedema
Pascal 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 patients
Lisa 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 imaging
John 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-cyclodextrin
Giampiero 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 generation
Carole Sargent, Julien Bauer, Muhamed Khalil, et al.
Clinical Genetics
|
August 13, 2019
Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family
Robert 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 male
Robert P Erickson, Steve Skinner, Hélène Jacquet, et al.
Page
of 12