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American Journal of Medical Genetics. Part A
|
February 3, 2007
Phenotypic spectrum of mosaic trisomy 18: two new patients, a literature review, and counseling issues
Megan E Tucker, Holly J Garringer, David D Weaver
Archives of Otolaryngology--Head & Neck Surgery
|
May 17, 2006
Hearing impairment susceptibility in elderly men and the DFNA18 locus
Holly J Garringer, Nathan D Pankratz, William C Nichols, et al.
Brain Structure & Function
|
September 26, 2009
Modeling familial British and Danish dementia
Holly J Garringer, Jill Murrell, Luciano D'Adamio, et al.
Neurobiology of Aging
|
January 29, 2017
Amyloid and intracellular accumulation of BRI<sub>2</sub>
Holly J Garringer, Neeraja Sammeta, Adrian Oblak, et al.
Plos One
|
February 19, 2013
Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice
Holly J Garringer, Jill Murrell, Neeraja Sammeta, et al.
The Journal of Biological Chemistry
|
November 20, 2009
Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration
Martin A Baraibar, Barry B Muhoberac, Holly J Garringer, et al.
Journal of the Neurological Sciences
|
May 15, 2014
A novel ferritin light chain mutation in neuroferritinopathy with an atypical presentation
Katsuya Nishida, Holly J Garringer, Naonobu Futamura, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 31, 2012
The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice
Ruben Vidal, Neeraja Sammeta, Holly J Garringer, et al.
Endocrinology
|
June 18, 2005
Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed
Tobias Larsson, Siobhan I Davis, Holly J Garringer, et al.
American Journal of Medical Genetics. Part A
|
September 14, 2007
Two novel GALNT3 mutations in familial tumoral calcinosis
Holly J Garringer, Seyed Mohammad Javad Mortazavi, Fatemehsadat Esteghamat, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics. Part A
|
February 3, 2007
Phenotypic spectrum of mosaic trisomy 18: two new patients, a literature review, and counseling issues
Megan E Tucker, Holly J Garringer, David D Weaver
Archives of Otolaryngology--Head & Neck Surgery
|
May 17, 2006
Hearing impairment susceptibility in elderly men and the DFNA18 locus
Holly J Garringer, Nathan D Pankratz, William C Nichols, et al.
Brain Structure & Function
|
September 26, 2009
Modeling familial British and Danish dementia
Holly J Garringer, Jill Murrell, Luciano D'Adamio, et al.
Neurobiology of Aging
|
January 29, 2017
Amyloid and intracellular accumulation of BRI<sub>2</sub>
Holly J Garringer, Neeraja Sammeta, Adrian Oblak, et al.
Plos One
|
February 19, 2013
Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice
Holly J Garringer, Jill Murrell, Neeraja Sammeta, et al.
The Journal of Biological Chemistry
|
November 20, 2009
Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration
Martin A Baraibar, Barry B Muhoberac, Holly J Garringer, et al.
Journal of the Neurological Sciences
|
May 15, 2014
A novel ferritin light chain mutation in neuroferritinopathy with an atypical presentation
Katsuya Nishida, Holly J Garringer, Naonobu Futamura, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 31, 2012
The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice
Ruben Vidal, Neeraja Sammeta, Holly J Garringer, et al.
Endocrinology
|
June 18, 2005
Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed
Tobias Larsson, Siobhan I Davis, Holly J Garringer, et al.
American Journal of Medical Genetics. Part A
|
September 14, 2007
Two novel GALNT3 mutations in familial tumoral calcinosis
Holly J Garringer, Seyed Mohammad Javad Mortazavi, Fatemehsadat Esteghamat, et al.
Page
of 5