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Scientific Reports
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July 29, 2017
Microfluidic Cell Retention Device for Perfusion of Mammalian Suspension Culture
Taehong Kwon, Holly Prentice, Jonas De Oliveira, et al.
Plos One
|
April 25, 2014
A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit
Gaël Manes, Pallavi Cheguru, Anurima Majumder, et al.
The Science of the Total Environment
|
October 11, 2014
Sensitivity analysis of a sediment dynamics model applied in a Mediterranean river basin: global change and management implications
M Sánchez-Canales, A López-Benito, V Acuña, et al.
Optics Express
|
June 13, 2014
Photonic molecules: tailoring the coupling strength and sign
S Haddadi, P Hamel, G Beaudoin, et al.
Journal Francais D'Ophtalmologie
|
October 6, 1998
[Clinical features and genetic analysis in a family with X-linked incomplete congenital stationary night blindness (CSNBi)]
C F Schmitt-Bernard, C Bareil, C P Hamel, et al.
Stem Cell Research
|
June 17, 2019
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy
Nejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, et al.
Brain Research. Molecular Brain Research
|
July 1, 1997
Identification of preferentially expressed cochlear genes by systematic sequencing of a rat cochlea cDNA library
A Soto-Prior, M Lavigne-Rebillard, M Lenoir, et al.
G3 (Bethesda, Md.)
|
December 13, 2024
A high copy suppressor screen identifies factors enhancing the allotopic production of subunit II of cytochrome c oxidase
Felipe Nieto-Panqueva, Miriam Vázquez-Acevedo, David F Barrera-Gómez, et al.
Journal of Alzheimer'S Disease : JAD
|
September 24, 2023
Multimodal Machine Learning for 10-Year Dementia Risk Prediction: The Framingham Heart Study
Huitong Ding, Amiya Mandapati, Alexander P Hamel, et al.
Molecular Therapy. Methods & Clinical Development
|
December 11, 2025
Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression Profiles
Carla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
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of 24
Search research articles
Search
Showing results (121-130 of 233) with videos related to
Sort By:
Page
of 24
Scientific Reports
|
July 29, 2017
Microfluidic Cell Retention Device for Perfusion of Mammalian Suspension Culture
Taehong Kwon, Holly Prentice, Jonas De Oliveira, et al.
Plos One
|
April 25, 2014
A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit
Gaël Manes, Pallavi Cheguru, Anurima Majumder, et al.
The Science of the Total Environment
|
October 11, 2014
Sensitivity analysis of a sediment dynamics model applied in a Mediterranean river basin: global change and management implications
M Sánchez-Canales, A López-Benito, V Acuña, et al.
Optics Express
|
June 13, 2014
Photonic molecules: tailoring the coupling strength and sign
S Haddadi, P Hamel, G Beaudoin, et al.
Journal Francais D'Ophtalmologie
|
October 6, 1998
[Clinical features and genetic analysis in a family with X-linked incomplete congenital stationary night blindness (CSNBi)]
C F Schmitt-Bernard, C Bareil, C P Hamel, et al.
Stem Cell Research
|
June 17, 2019
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy
Nejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, et al.
Brain Research. Molecular Brain Research
|
July 1, 1997
Identification of preferentially expressed cochlear genes by systematic sequencing of a rat cochlea cDNA library
A Soto-Prior, M Lavigne-Rebillard, M Lenoir, et al.
G3 (Bethesda, Md.)
|
December 13, 2024
A high copy suppressor screen identifies factors enhancing the allotopic production of subunit II of cytochrome c oxidase
Felipe Nieto-Panqueva, Miriam Vázquez-Acevedo, David F Barrera-Gómez, et al.
Journal of Alzheimer'S Disease : JAD
|
September 24, 2023
Multimodal Machine Learning for 10-Year Dementia Risk Prediction: The Framingham Heart Study
Huitong Ding, Amiya Mandapati, Alexander P Hamel, et al.
Molecular Therapy. Methods & Clinical Development
|
December 11, 2025
Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression Profiles
Carla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
Page
of 24