Related references
Note: Only part of the references are listed.BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes
Qihong Zhang et al.
HUMAN MOLECULAR GENETICS (2012)
Preparation of Mouse Embryonic Fibroblast Cells Suitable for Culturing Human Embryonic and Induced Pluripotent Stem Cells
Justyna Jozefczuk et al.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS (2012)
TUDCA Slows Retinal Degeneration in Two Different Mouse Models of Retinitis Pigmentosa and Prevents Obesity in Bardet-Biedl Syndrome Type 1 Mice
Arlene V. Drack et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2012)
BBS Mutational Analysis: A Strategic Approach
Gail Billingsley et al.
OPHTHALMIC GENETICS (2011)
Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model
David L. Simons et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes
Qihong Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened
Seongjin Seo et al.
PLOS GENETICS (2011)
The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia
Hua Jin et al.
CELL (2010)
Lack of cadherins Celsr2 and Celsr3 impairs ependymal ciliogenesis, leading to fatal hydrocephalus
Fadel Tissir et al.
NATURE NEUROSCIENCE (2010)
BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly
Seongjin Seo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling
Seongjin Seo et al.
HUMAN MOLECULAR GENETICS (2009)
A BBSome Subunit Links Ciliogenesis, Microtubule Stability, and Acetylation
Alexander V. Loktev et al.
DEVELOPMENTAL CELL (2008)
Mutations in Hydin impair ciliary motility in mice
Karl-Ferdinand Lechtreck et al.
JOURNAL OF CELL BIOLOGY (2008)
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome
Kamal Rahmouni et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia
Alok S. Shah et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
Maxence V. Nachury et al.
CELL (2007)
Pronuclear injection for the production of transgenic mice
Lars M. Ittner et al.
NATURE PROTOCOLS (2007)
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity
Erica R. Eichers et al.
HUMAN GENETICS (2006)
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression
JC Kim et al.
NATURE GENETICS (2004)
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly
K Mykytyn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method
KJ Livak et al.
METHODS (2001)
Share Paper
