相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Photoreceptor cilia, in contrast to primary cilia, grant entry to a partially assembled BBSome
Ying Hsu et al.
HUMAN MOLECULAR GENETICS (2021)
Bardet-Biedl syndrome 3 protein promotes ciliary exit of the signaling protein phospholipase D via the BBSome
Yan-Xia Liu et al.
ELIFE (2021)
BBSome ablation in SF1 neurons causes obesity without comorbidities
Mohamed Rouabhi et al.
MOLECULAR METABOLISM (2021)
BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human development
K. Benardais et al.
CELL AND TISSUE RESEARCH (2021)
Endothelial BBSome is essential for vascular, metabolic, and retinal functions
Jingwei Jiang et al.
MOLECULAR METABOLISM (2021)
Bardet-Biedl syndrome proteins regulate intracellular signaling and neuronal function in patient-specific iPSC-derived neurons
Liheng Wang et al.
JOURNAL OF CLINICAL INVESTIGATION (2021)
Sex-Dependent Effects of Nephron Ift88 Disruption on BP, Renal Function, and Cystogenesis
Chunyan Hu et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2021)
Chlamydomonas LZTFL1 mediates phototaxis via controlling BBSome recruitment to the basal body and its reassembly at the ciliary tip
Wei-Yue Sun et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2021)
The morbid genome of ciliopathies: an update
Hanan E. Shamseldin et al.
GENETICS IN MEDICINE (2020)
Cardiovascular Regulation by the Neuronal BBSome
Deng-Fu Guo et al.
HYPERTENSION (2020)
Bardet-Biedl syndrome obesity: BBS4 regulates cellular ER stress in early adipogenesis
Mariana Anosov et al.
MOLECULAR GENETICS AND METABOLISM (2019)
Identification and Characterization o Known Biallelic Mutations in the IFT27 (BBS19) Gene in a Novel Family With Bardet-Biedl Syndrome
Elise Schaefer et al.
FRONTIERS IN GENETICS (2019)
The Role of Primary Cilia in the Crosstalk between the Ubiquitin-Proteasome System and Autophagy
Antonia Wiegering et al.
CELLS (2019)
The BBSome in POMC and AgRP Neurons Is Necessary for Body Weight Regulation and Sorting of Metabolic Receptors
Deng-Fu Guo et al.
DIABETES (2019)
The Bardet-Biedl syndrome protein complex regulates cell migration and tissue repair through a Cullin-3/RhoA pathway
Deng-Fu Guo et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2019)
Smooth Muscle Cell-Specific Disruption of the BBSome Causes Vascular Dysfunction
John J. Reho et al.
HYPERTENSION (2019)
The Endocrine and Metabolic Characteristics of a Large Bardet-Biedl Syndrome Clinic Population
Safa Mujahid et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2018)
Lztfl1/BBS17 controls energy homeostasis by regulating the leptin signaling in the hypothalamic neurons
Qun Wei et al.
JOURNAL OF MOLECULAR CELL BIOLOGY (2018)
Role of Alstrom syndrome 1 in the regulation of blood pressure and renal function
Ankita Bachhawat Jaykumar et al.
JCI INSIGHT (2018)
Risk Factors for Severe Renal Disease in Barden-Biedl Syndrome
Elizabeth Forsythe et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2017)
Ciliary Mechanisms of Cyst Formation in Polycystic Kidney Disease
Ming Ma et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2017)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
Audrey E. Hendricks et al.
SCIENTIFIC REPORTS (2017)
Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein
Charles Anthony Scott et al.
PLOS GENETICS (2017)
Bardet-Biedl Syndrome as a Chaperonopathy: Dissecting the Major Role of Chaperonin-Like BBS Proteins (BBS6-BBS10-BBS12)
Maria Alvarez-Satta et al.
FRONTIERS IN MOLECULAR BIOSCIENCES (2017)
The BBSome Controls Energy Homeostasis by Mediating the Transport of the Leptin Receptor to the Plasma Membrane
Deng-Fu Guo et al.
PLOS GENETICS (2016)
Vascular Endothelial Primary Cilia: Mechanosensation and Hypertensiony
Ashraf M. Mohieldin et al.
CURRENT HYPERTENSION REVIEWS (2016)
Regulation of Insulin Receptor Trafficking by Bardet Biedl Syndrome Proteins
Rachel D. Starks et al.
PLOS GENETICS (2015)
A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
Elaine T. Lim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Bardet-Biedl syndrome proteins 1 and 3 regulate the ciliary trafficking of polycystic kidney disease 1 protein
Xuefeng Su et al.
HUMAN MOLECULAR GENETICS (2014)
Basal body proteins regulate Notch signaling through endosomal trafficking
Carmen C. Leitch et al.
JOURNAL OF CELL SCIENCE (2014)
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators
Yangfan P. Liu et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
Cilia and coordination of signaling networks during heart development
Karen Koefoed et al.
ORGANOGENESIS (2014)
Assembling a primary cilium
Sehyun Kim et al.
CURRENT OPINION IN CELL BIOLOGY (2013)
Bardet-Biedl syndrome proteins control the cilia length through regulation of actin polymerization
Victor Hernandez-Hernandez et al.
HUMAN MOLECULAR GENETICS (2013)
Neuropeptide Y Family Receptors Traffic via the Bardet-Biedl Syndrome Pathway to Signal in Neuronal Primary Cilia
Alexander V. Loktev et al.
CELL REPORTS (2013)
Intrinsic Protein-Protein Interaction-mediated and Chaperonin-assisted Sequential Assembly of Stable Bardet-Biedl Syndrome Protein Complex, the BBSome
Qihong Zhang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Direct role of Bardet-Biedl syndrome proteins in transcriptional regulation
Cecilia Gascue et al.
JOURNAL OF CELL SCIENCE (2012)
Neocortical and Hippocampal Volume Loss in a Human Ciliopathy: A Quantitative MRI Study in Bardet-Biedl Syndrome
Kate Baker et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)
Kim M. Keppler-Noreuil et al.
BMC MEDICAL GENETICS (2011)
Bardet-Biedl Syndrome: A Study of the Renal and Cardiovascular Phenotypes in a French Cohort
Olivier Imhoff et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2011)
Bardet-Biedl syndrome highlights the major role of the primary cilium in efficient water reabsorption
Vincent Marion et al.
KIDNEY INTERNATIONAL (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)
Inactivation of Bardet-Biedl syndrome genes causes kidney defects
Deng-Fu Guo et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2011)
Contrasting vascular effects caused by loss of Bardet-Biedl syndrome genes
Andreas M. Beyer et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2010)
The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia
Hua Jin et al.
CELL (2010)
Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling
Seongjin Seo et al.
HUMAN MOLECULAR GENETICS (2009)
TRIM32 is an E3 ubiquitin ligase for dysbindin
Matthew Locke et al.
HUMAN MOLECULAR GENETICS (2009)
Autosomal recessive Bardet-Biedl syndrome: first-degree relatives have no predisposition to metabolic and renal disorders
Michael P. Webb et al.
KIDNEY INTERNATIONAL (2009)
Dissociation between sympathetic nerve traffic and sympathetically mediated vascular tone in normotensive human obesity
Alexei Vasilievich Agapitov et al.
HYPERTENSION (2008)
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome
Kamal Rahmouni et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Restoration of renal function in zebrafish models of ciliopathies
Jonathan L. Tobin et al.
PEDIATRIC NEPHROLOGY (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 knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity
Roger E. Davis et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Disruption of the basal body comprises proteasomal function and perturbs intracellular Wnt response
Jantje M. Gerdes et al.
NATURE GENETICS (2007)
Loss of Bardet-Biedl syndrome proteins causes defects in peripheral sensory innervation and function
Perciliz L. Tan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Differences in renal tubule primary cilia length in a mouse model of Bardet- Biedl syndrome
Elaine M. Mokrzan et al.
NEPHRON EXPERIMENTAL NEPHROLOGY (2007)
Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians
Michael Benzinou et al.
DIABETES (2006)
The primary cilium as the cell's antenna: Signaling at a sensory organelle
Veena Singla et al.
SCIENCE (2006)
Homozygosity mapping with SNP arrays identifies TRIM32 an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)
AP Chiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function
HJ Yen et al.
HUMAN MOLECULAR GENETICS (2006)
An incredible decade for the primary cilium: a look at a once-forgotten organelle
JR Davenport et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2005)
MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis
JC Kim et al.
JOURNAL OF CELL SCIENCE (2005)
Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study
SJ Moore et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737(orpk) mutant mice
QH Zhang et al.
LABORATORY INVESTIGATION (2005)
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)
Comparative and basal genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
JB Li et al.
CELL (2004)
Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2
JL Badano et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Intraflagellar transport
JL Rosenbaum et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2002)
Molecular mechanisms of human hypertension
RP Lifton et al.
CELL (2001)
分享论文
