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Cell
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May 14, 2011
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
Liyun Sang, Julie J Miller, Kevin C Corbit, et al.
Clinical Genetics
|
August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
A Chaudhry, A Noor, B Degagne, et al.
American Journal of Human Genetics
|
October 28, 2008
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290
Nicholas T Gorden, Heleen H Arts, Melissa A Parisi, et al.
Science (New York, N.Y.)
|
May 15, 2012
Vesta's shape and morphology
R Jaumann, D A Williams, D L Buczkowski, et al.
Science (New York, N.Y.)
|
August 24, 2019
Images from the surface of asteroid Ryugu show rocks similar to carbonaceous chondrite meteorites
R Jaumann, N Schmitz, T-M Ho, et al.
Science (New York, N.Y.)
|
November 19, 2016
Rosetta's comet 67P/Churyumov-Gerasimenko sheds its dusty mantle to reveal its icy nature
S Fornasier, S Mottola, H U Keller, et al.
Science (New York, N.Y.)
|
October 29, 2011
Images of asteroid 21 Lutetia: a remnant planetesimal from the early Solar System
H Sierks, P Lamy, C Barbieri, et al.
Science (New York, N.Y.)
|
March 23, 2017
Surface changes on comet 67P/Churyumov-Gerasimenko suggest a more active past
M Ramy El-Maarry, O Groussin, N Thomas, et al.
Science Translational Medicine
|
September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability
Abdul Noor, Annabel Whibley, Christian R Marshall, et al.
Nature Communications
|
July 30, 2024
Evidence for multi-fragmentation and mass shedding of boulders on rubble-pile binary asteroid system (65803) Didymos
M Pajola, F Tusberti, A Lucchetti, et al.
Page
of 56
Search research articles
Search
Showing results (511-520 of 551) with videos related to
Sort By:
Page
of 56
Cell
|
May 14, 2011
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
Liyun Sang, Julie J Miller, Kevin C Corbit, et al.
Clinical Genetics
|
August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
A Chaudhry, A Noor, B Degagne, et al.
American Journal of Human Genetics
|
October 28, 2008
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290
Nicholas T Gorden, Heleen H Arts, Melissa A Parisi, et al.
Science (New York, N.Y.)
|
May 15, 2012
Vesta's shape and morphology
R Jaumann, D A Williams, D L Buczkowski, et al.
Science (New York, N.Y.)
|
August 24, 2019
Images from the surface of asteroid Ryugu show rocks similar to carbonaceous chondrite meteorites
R Jaumann, N Schmitz, T-M Ho, et al.
Science (New York, N.Y.)
|
November 19, 2016
Rosetta's comet 67P/Churyumov-Gerasimenko sheds its dusty mantle to reveal its icy nature
S Fornasier, S Mottola, H U Keller, et al.
Science (New York, N.Y.)
|
October 29, 2011
Images of asteroid 21 Lutetia: a remnant planetesimal from the early Solar System
H Sierks, P Lamy, C Barbieri, et al.
Science (New York, N.Y.)
|
March 23, 2017
Surface changes on comet 67P/Churyumov-Gerasimenko suggest a more active past
M Ramy El-Maarry, O Groussin, N Thomas, et al.
Science Translational Medicine
|
September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability
Abdul Noor, Annabel Whibley, Christian R Marshall, et al.
Nature Communications
|
July 30, 2024
Evidence for multi-fragmentation and mass shedding of boulders on rubble-pile binary asteroid system (65803) Didymos
M Pajola, F Tusberti, A Lucchetti, et al.
Page
of 56