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Michael A Walter

Showing results (51-60 of 56) with videos related to

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Investigative Ophthalmology & Visual Science|May 31, 2002
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletionsOrdan J Lehmann, Neil D Ebenezer, Rosemary Ekong, et al.
Cancer Research|April 22, 2010
FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancerPartha S Ray, Jinhua Wang, Ying Qu, et al.
Human Molecular Genetics|October 30, 2009
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomaliesMing Ye, Karyn M Berry-Wynne, Mika Asai-Coakwell, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 21, 2014
FOXA1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotypeDavid J DeGraff, Magdalena M Grabowska, Tom C Case, et al.
Human Molecular Genetics|December 19, 2018
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucomaAdrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
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Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Investigative Ophthalmology & Visual Science|May 31, 2002
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletionsOrdan J Lehmann, Neil D Ebenezer, Rosemary Ekong, et al.
Cancer Research|April 22, 2010
FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancerPartha S Ray, Jinhua Wang, Ying Qu, et al.
Human Molecular Genetics|October 30, 2009
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomaliesMing Ye, Karyn M Berry-Wynne, Mika Asai-Coakwell, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 21, 2014
FOXA1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotypeDavid J DeGraff, Magdalena M Grabowska, Tom C Case, et al.
Human Molecular Genetics|December 19, 2018
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucomaAdrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
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