213 related articles for article (PubMed ID: 24695551)
1. Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse model.
Agassandian K; Patel M; Agassandian M; Steren KE; Rahmouni K; Sheffield VC; Card JP
PLoS One; 2014; 9(4):e93484. PubMed ID: 24695551
[TBL] [Abstract][Full Text] [Related]
2. Ciliary Defects in a Mouse Model of Bardet-Biedl Syndrome are Selectively Pronounced in Brian Regions Involved in Cardiovascular Regulation.
Agassandian C; Patel M; Bakotic B; Agassandian K
Ross Fiziol Zh Im I M Sechenova; 2016 Aug; 102(8):904-20. PubMed ID: 30193056
[TBL] [Abstract][Full Text] [Related]
3. Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly.
Mykytyn K; Mullins RF; Andrews M; Chiang AP; Swiderski RE; Yang B; Braun T; Casavant T; Stone EM; Sheffield VC
Proc Natl Acad Sci U S A; 2004 Jun; 101(23):8664-9. PubMed ID: 15173597
[TBL] [Abstract][Full Text] [Related]
4. Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null mice.
Chamling X; Seo S; Bugge K; Searby C; Guo DF; Drack AV; Rahmouni K; Sheffield VC
PLoS One; 2013; 8(3):e59101. PubMed ID: 23554981
[TBL] [Abstract][Full Text] [Related]
5. A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity.
Davis RE; Swiderski RE; Rahmouni K; Nishimura DY; Mullins RF; Agassandian K; Philp AR; Searby CC; Andrews MP; Thompson S; Berry CJ; Thedens DR; Yang B; Weiss RM; Cassell MD; Stone EM; Sheffield VC
Proc Natl Acad Sci U S A; 2007 Dec; 104(49):19422-7. PubMed ID: 18032602
[TBL] [Abstract][Full Text] [Related]
6. Differences in renal tubule primary cilia length in a mouse model of Bardet-Biedl syndrome.
Mokrzan EM; Lewis JS; Mykytyn K
Nephron Exp Nephrol; 2007; 106(3):e88-96. PubMed ID: 17519557
[TBL] [Abstract][Full Text] [Related]
7. BBS4 is required for intraflagellar transport coordination and basal body number in mammalian olfactory cilia.
Uytingco CR; Williams CL; Xie C; Shively DT; Green WW; Ukhanov K; Zhang L; Nishimura DY; Sheffield VC; Martens JR
J Cell Sci; 2019 Feb; 132(5):. PubMed ID: 30665891
[TBL] [Abstract][Full Text] [Related]
8. Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia.
Bennouna-Greene V; Kremer S; Stoetzel C; Christmann D; Schuster C; Durand M; Verloes A; Sigaudy S; Holder-Espinasse M; Godet J; Brandt C; Marion V; Danion A; Dietemann JL; Dollfus H
Clin Genet; 2011 Dec; 80(6):523-31. PubMed ID: 21517826
[TBL] [Abstract][Full Text] [Related]
9. Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia.
Shah AS; Farmen SL; Moninger TO; Businga TR; Andrews MP; Bugge K; Searby CC; Nishimura D; Brogden KA; Kline JN; Sheffield VC; Welsh MJ
Proc Natl Acad Sci U S A; 2008 Mar; 105(9):3380-5. PubMed ID: 18299575
[TBL] [Abstract][Full Text] [Related]
10. Bardet-Biedl syndrome: Is it only cilia dysfunction?
Novas R; Cardenas-Rodriguez M; Irigoín F; Badano JL
FEBS Lett; 2015 Nov; 589(22):3479-91. PubMed ID: 26231314
[TBL] [Abstract][Full Text] [Related]
11. Bardet-Biedl syndrome proteins control the cilia length through regulation of actin polymerization.
Hernandez-Hernandez V; Pravincumar P; Diaz-Font A; May-Simera H; Jenkins D; Knight M; Beales PL
Hum Mol Genet; 2013 Oct; 22(19):3858-68. PubMed ID: 23716571
[TBL] [Abstract][Full Text] [Related]
12. BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human development.
Bénardais K; Delfino G; Samama B; Devys D; Antal MC; Ghandour MS; Boehm N
Cell Tissue Res; 2021 Jul; 385(1):37-48. PubMed ID: 33860840
[TBL] [Abstract][Full Text] [Related]
13. A mouse model of Bardet-Biedl Syndrome has impaired fear memory, which is rescued by lithium treatment.
Pak TK; Carter CS; Zhang Q; Huang SC; Searby C; Hsu Y; Taugher RJ; Vogel T; Cychosz CC; Genova R; Moreira NN; Stevens H; Wemmie JA; Pieper AA; Wang K; Sheffield VC
PLoS Genet; 2021 Apr; 17(4):e1009484. PubMed ID: 33886537
[TBL] [Abstract][Full Text] [Related]
14. BBS mutations modify phenotypic expression of CEP290-related ciliopathies.
Zhang Y; Seo S; Bhattarai S; Bugge K; Searby CC; Zhang Q; Drack AV; Stone EM; Sheffield VC
Hum Mol Genet; 2014 Jan; 23(1):40-51. PubMed ID: 23943788
[TBL] [Abstract][Full Text] [Related]
15. Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia.
Berbari NF; Lewis JS; Bishop GA; Askwith CC; Mykytyn K
Proc Natl Acad Sci U S A; 2008 Mar; 105(11):4242-6. PubMed ID: 18334641
[TBL] [Abstract][Full Text] [Related]
16. Bardet-Biedl Syndrome ciliopathy is linked to altered hematopoiesis and dysregulated self-tolerance.
Tsyklauri O; Niederlova V; Forsythe E; Prasai A; Drobek A; Kasparek P; Sparks K; Trachtulec Z; Prochazka J; Sedlacek R; Beales P; Huranova M; Stepanek O
EMBO Rep; 2021 Feb; 22(2):e50785. PubMed ID: 33426789
[TBL] [Abstract][Full Text] [Related]
17. Neocortical and hippocampal volume loss in a human ciliopathy: A quantitative MRI study in Bardet-Biedl syndrome.
Baker K; Northam GB; Chong WK; Banks T; Beales P; Baldeweg T
Am J Med Genet A; 2011 Jan; 155A(1):1-8. PubMed ID: 21204204
[TBL] [Abstract][Full Text] [Related]
18. The BBSome assembly is spatially controlled by BBS1 and BBS4 in human cells.
Prasai A; Schmidt Cernohorska M; Ruppova K; Niederlova V; Andelova M; Draber P; Stepanek O; Huranova M
J Biol Chem; 2020 Oct; 295(42):14279-14290. PubMed ID: 32759308
[TBL] [Abstract][Full Text] [Related]
19. Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome.
Rahmouni K; Fath MA; Seo S; Thedens DR; Berry CJ; Weiss R; Nishimura DY; Sheffield VC
J Clin Invest; 2008 Apr; 118(4):1458-67. PubMed ID: 18317593
[TBL] [Abstract][Full Text] [Related]
20. Bardet-Biedl syndrome-8 (BBS8) protein is crucial for the development of outer segments in photoreceptor neurons.
Dilan TL; Singh RK; Saravanan T; Moye A; Goldberg AFX; Stoilov P; Ramamurthy V
Hum Mol Genet; 2018 Jan; 27(2):283-294. PubMed ID: 29126234
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
