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Plos Genetics
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December 17, 2013
Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain
Sebiha Cevik, Anna A W M Sanders, Erwin Van Wijk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 22, 2020
PCARE and WASF3 regulate ciliary F-actin assembly that is required for the initiation of photoreceptor outer segment disk formation
Julio C Corral-Serrano, Ideke J C Lamers, Jeroen van Reeuwijk, et al.
American Journal of Human Genetics
|
September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
Konstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Human Molecular Genetics
|
December 12, 2017
DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport
Verity L Hartill, Glenn van de Hoek, Mitali P Patel, et al.
Clinical Chemistry and Laboratory Medicine
|
June 17, 2009
Approaching clinical proteomics: current state and future fields of application in fluid proteomics
Rolf Apweiler, Charalampos Aslanidis, Thomas Deufel, et al.
Ophthalmology
|
July 28, 2020
Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK Consortium
Anita de Breuk, Ilhan E Acar, Eveline Kersten, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology
|
September 10, 2009
Approaching clinical proteomics: current state and future fields of application in cellular proteomics
Rolf Apweiler, Charalampos Aslanidis, Thomas Deufel, et al.
JMIR Medical Informatics
|
December 5, 2024
EyeMatics: An Ophthalmology Use Case Within the German Medical Informatics Initiative
Julian Varghese, Alexander Schuster, Broder Poschkamp, et al.
The Journal of Clinical Investigation
|
May 27, 2020
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome
Brooke L Latour, Julie C Van De Weghe, Tamara Ds Rusterholz, et al.
Nature Communications
|
June 6, 2015
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
Miriam Schmidts, Yuqing Hou, Claudio R Cortés, et al.
Page
of 30
Search research articles
Search
Showing results (271-280 of 296) with videos related to
Sort By:
Page
of 30
Plos Genetics
|
December 17, 2013
Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain
Sebiha Cevik, Anna A W M Sanders, Erwin Van Wijk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 22, 2020
PCARE and WASF3 regulate ciliary F-actin assembly that is required for the initiation of photoreceptor outer segment disk formation
Julio C Corral-Serrano, Ideke J C Lamers, Jeroen van Reeuwijk, et al.
American Journal of Human Genetics
|
September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
Konstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Human Molecular Genetics
|
December 12, 2017
DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport
Verity L Hartill, Glenn van de Hoek, Mitali P Patel, et al.
Clinical Chemistry and Laboratory Medicine
|
June 17, 2009
Approaching clinical proteomics: current state and future fields of application in fluid proteomics
Rolf Apweiler, Charalampos Aslanidis, Thomas Deufel, et al.
Ophthalmology
|
July 28, 2020
Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK Consortium
Anita de Breuk, Ilhan E Acar, Eveline Kersten, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology
|
September 10, 2009
Approaching clinical proteomics: current state and future fields of application in cellular proteomics
Rolf Apweiler, Charalampos Aslanidis, Thomas Deufel, et al.
JMIR Medical Informatics
|
December 5, 2024
EyeMatics: An Ophthalmology Use Case Within the German Medical Informatics Initiative
Julian Varghese, Alexander Schuster, Broder Poschkamp, et al.
The Journal of Clinical Investigation
|
May 27, 2020
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome
Brooke L Latour, Julie C Van De Weghe, Tamara Ds Rusterholz, et al.
Nature Communications
|
June 6, 2015
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
Miriam Schmidts, Yuqing Hou, Claudio R Cortés, et al.
Page
of 30