Product References
High-efficient CRISPR/Cas9-mediated gene targeting to establish cell models of ciliopathies.
Methods in cell biology
Hosoba K,Morita T,Zhang Y,Kishi H,Yamamoto T,Miyamoto T
Tue Mar 28 00:00:00 UTC 2023
Interactions between TULP3 tubby domain and ARL13B amphipathic helix promote lipidated protein transport to cilia.
Molecular biology of the cell
Palicharla VR,Hwang SH,Somatilaka BN,Legué E,Shimada IS,Familiari NE,Tran VM,Woodruff JB,Liem KF,Mukhopadhyay S
Wed Mar 01 00:00:00 UTC 2023
INPP5E controls ciliary localization of phospholipids and the odor response in olfactory sensory neurons.
Journal of cell science
Ukhanov K,Uytingco C,Green W,Zhang L,Schurmans S,Martens JR
Tue Mar 01 00:00:00 UTC 2022
Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E.
Molecular biology of the cell
Dewees SI,Vargová R,Hardin KR,Turn RE,Devi S,Linnert J,Wolfrum U,Caspary T,Eliáš M,Kahn RA
Fri Apr 01 00:00:00 UTC 2022
Multiple ciliary localization signals control INPP5E ciliary targeting.
eLife
Cilleros-Rodriguez D,Martin-Morales R,Barbeito P,Deb Roy A,Loukil A,Sierra-Rodero B,Herranz G,Pampliega O,Redrejo-Rodriguez M,Goetz SC,Izquierdo M,Inoue T,Garcia-Gonzalo FR
Mon Sep 05 00:00:00 UTC 2022
The ciliary gene INPP5E confers dorsal telencephalic identity to human cortical organoids by negatively regulating Sonic hedgehog signaling.
Cell reports
Schembs L,Willems A,Hasenpusch-Theil K,Cooper JD,Whiting K,Burr K,Bøstrand SMK,Selvaraj BT,Chandran S,Theil T
Tue May 17 00:00:00 UTC 2022
Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling.
JCI insight
Shi H,Wang H,Zhang C,Lu Y,Yao J,Chen Z,Xing G,Wei Q,Cao X
Tue Feb 22 00:00:00 UTC 2022
The ARF GAPs ELMOD1 and ELMOD3 act at the Golgi and cilia to regulate ciliogenesis and ciliary protein traffic.
Molecular biology of the cell
Turn RE,Hu Y,Dewees SI,Devi N,East MP,Hardin KR,Khatib T,Linnert J,Wolfrum U,Lim MJ,Casanova JE,Caspary T,Kahn RA
Tue Feb 01 00:00:00 UTC 2022
Differential Roles of Tubby Family Proteins in Ciliary Formation and Trafficking.
Molecules and cells
Hong JJ,Kim KE,Park SY,Bok J,Seo JT,Moon SJ
Tue Aug 31 00:00:00 UTC 2021
Exocyst complex mediates recycling of internal cilia.
Current biology : CB
Rivera-Molina FE,Xi Z,Reales E,Wang B,Toomre D
Mon Dec 20 00:00:00 UTC 2021
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics
Luo M,Lin Z,Zhu T,Jin M,Meng D,He R,Cao Z,Shen Y,Lu C,Cai R,Zhao Y,Wang X,Li H,Wu S,Zou X,Luo G,Cao L,Huang M,Jiao H,Gao H,Sui R,Zhao C,Ma X,Cao M
Tue Jun 01 00:00:00 UTC 2021
Deletion of the phosphatase INPP5E in the murine retina impairs photoreceptor axoneme formation and prevents disc morphogenesis.
The Journal of biological chemistry
Sharif AS,Gerstner CD,Cady MA,Arshavsky VY,Mitchell C,Ying G,Frederick JM,Baehr W
Mon Aug 23 00:00:00 UTC 2021
Deletion of the phosphatase INPP5E in the murine retina impairs photoreceptor axoneme formation and prevents disc morphogenesis.
The Journal of biological chemistry
Sharif AS,Gerstner CD,Cady MA,Arshavsky VY,Mitchell C,Ying G,Frederick JM,Baehr W
Mon Aug 23 00:00:00 UTC 2021
Ciliopathy protein HYLS1 coordinates the biogenesis and signaling of primary cilia by activating the ciliary lipid kinase PIPKIγ.
Science advances
Chen C,Xu Q,Zhang Y,Davies BA,Huang Y,Katzmann DJ,Harris PC,Hu J,Ling K
Tue Jun 01 00:00:00 UTC 2021
Down-Regulation of Inpp5e Associated With Abnormal Ciliogenesis During Embryonic Neurodevelopment Under Inositol Deficiency.
Frontiers in neurology
Yue H,Li S,Qin J,Gao T,Lyu J,Liu Y,Wang X,Guan Z,Zhu Z,Niu B,Zhong R,Guo J,Wang J
Sat Nov 11 00:00:00 UTC 2023
Interaction of INPP5E with ARL13B is essential for its ciliary membrane retention but dispensable for its ciliary entry.
Biology open
Qiu H,Fujisawa S,Nozaki S,Katoh Y,Nakayama K
Mon Jan 25 00:00:00 UTC 2021
ARL3 and ARL13B GTPases participate in distinct steps of INPP5E targeting to the ciliary membrane.
Biology open
Fujisawa S,Qiu H,Nozaki S,Chiba S,Katoh Y,Nakayama K
Wed Sep 15 00:00:00 UTC 2021
The autophagy protein ATG16L1 cooperates with IFT20 and INPP5E to regulate the turnover of phosphoinositides at the primary cilium.
Cell reports
Boukhalfa A,Roccio F,Dupont N,Codogno P,Morel E
Tue Apr 27 00:00:00 UTC 2021
The autophagy protein ATG16L1 cooperates with IFT20 and INPP5E to regulate the turnover of phosphoinositides at the primary cilium.
Cell reports
Boukhalfa A,Roccio F,Dupont N,Codogno P,Morel E
Tue Apr 27 00:00:00 UTC 2021
The Major Ciliary Isoforms of RPGR Build Different Interaction Complexes with INPP5E and RPGRIP1L.
International journal of molecular sciences
Vössing C,Atigbire P,Eilers J,Markus F,Stieger K,Song F,Neidhardt J
Tue Mar 30 00:00:00 UTC 2021
Genetic interaction of mammalian IFT-A paralogs regulates cilia disassembly, ciliary entry of membrane protein, Hedgehog signaling, and embryogenesis.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Wang W,Allard BA,Pottorf TS,Wang HH,Vivian JL,Tran PV
Fri May 01 00:00:00 UTC 2020
ARL13B regulates Sonic hedgehog signaling from outside primary cilia.
eLife
Gigante ED,Taylor MR,Ivanova AA,Kahn RA,Caspary T
Wed Mar 04 00:00:00 UTC 2020
Loss of polycystins suppresses deciliation via the activation of the centrosomal integrity pathway.
Life science alliance
Gerakopoulos V,Ngo P,Tsiokas L
Tue Sep 01 00:00:00 UTC 2020
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRP.
Proceedings of the National Academy of Sciences of the United States of America
Zhang Q,Giacalone JC,Searby C,Stone EM,Tucker BA,Sheffield VC
Tue Jan 22 00:00:00 UTC 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRP.
Proceedings of the National Academy of Sciences of the United States of America
Zhang Q,Giacalone JC,Searby C,Stone EM,Tucker BA,Sheffield VC
Tue Jan 22 00:00:00 UTC 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRP.
Proceedings of the National Academy of Sciences of the United States of America
Zhang Q,Giacalone JC,Searby C,Stone EM,Tucker BA,Sheffield VC
Tue Jan 22 00:00:00 UTC 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRP.
Proceedings of the National Academy of Sciences of the United States of America
Zhang Q,Giacalone JC,Searby C,Stone EM,Tucker BA,Sheffield VC
Tue Jan 22 00:00:00 UTC 2019
Development of a Molecularly Stable Gene Therapy Vector for the Treatment of RPGR-Associated X-Linked Retinitis Pigmentosa.
Human gene therapy
Giacalone JC,Andorf JL,Zhang Q,Burnight ER,Ochoa D,Reutzel AJ,Collins MM,Sheffield VC,Mullins RF,Han IC,Stone EM,Tucker BA
Thu Aug 01 00:00:00 UTC 2019
TULP3 is required for localization of membrane-associated proteins ARL13B and INPP5E to primary cilia.
Biochemical and biophysical research communications
Han S,Miyoshi K,Shikada S,Amano G,Wang Y,Yoshimura T,Katayama T
Tue Jan 29 00:00:00 UTC 2019
TULP3 is required for localization of membrane-associated proteins ARL13B and INPP5E to primary cilia.
Biochemical and biophysical research communications
Han S,Miyoshi K,Shikada S,Amano G,Wang Y,Yoshimura T,Katayama T
Tue Jan 29 00:00:00 UTC 2019
Tulp3 Regulates Renal Cystogenesis by Trafficking of Cystoproteins to Cilia.
Current biology : CB
Hwang SH,Somatilaka BN,Badgandi H,Palicharla VR,Walker R,Shelton JM,Qian F,Mukhopadhyay S
Mon Mar 04 00:00:00 UTC 2019
A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling.
Cell reports
Frikstad KM,Molinari E,Thoresen M,Ramsbottom SA,Hughes F,Letteboer SJF,Gilani S,Schink KO,Stokke T,Geimer S,Pedersen LB,Giles RH,Akhmanova A,Roepman R,Sayer JA,Patzke S
Tue Aug 13 00:00:00 UTC 2019
The ciliary GTPase Arl3 maintains tissue architecture by directing planar spindle orientation during epidermal morphogenesis.
Development (Cambridge, England)
Bhattarai SR,Begum S,Popow R,Ezratty EJ
Fri May 10 00:00:00 UTC 2019
ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition.
American journal of human genetics
Alkanderi S,Molinari E,Shaheen R,Elmaghloob Y,Stephen LA,Sammut V,Ramsbottom SA,Srivastava S,Cairns G,Edwards N,Rice SJ,Ewida N,Alhashem A,White K,Miles CG,Steel DH,Alkuraya FS,Ismail S,Sayer JA
Thu Oct 04 00:00:00 UTC 2018
ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition.
American journal of human genetics
Alkanderi S,Molinari E,Shaheen R,Elmaghloob Y,Stephen LA,Sammut V,Ramsbottom SA,Srivastava S,Cairns G,Edwards N,Rice SJ,Ewida N,Alhashem A,White K,Miles CG,Steel DH,Alkuraya FS,Ismail S,Sayer JA
Thu Oct 04 00:00:00 UTC 2018
Characterization of Primary Cilia in Normal Fallopian Tube Epithelium and Serous Tubal Intraepithelial Carcinoma.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
Abdelhamed ZA,Ryan TA,Fuller M,Coulson-Gilmer C,Abdelmottaleb DI,Wang TL,Kaun JC,Wang P,Hutson R,Wilkinson N,Bell SM,Johnson CA
Mon Oct 01 00:00:00 UTC 2018
Characterization of Primary Cilia in Normal Fallopian Tube Epithelium and Serous Tubal Intraepithelial Carcinoma.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
Abdelhamed ZA,Ryan TA,Fuller M,Coulson-Gilmer C,Abdelmottaleb DI,Wang TL,Kaun JC,Wang P,Hutson R,Wilkinson N,Bell SM,Johnson CA
Mon Oct 01 00:00:00 UTC 2018
The Joubert Syndrome Protein Inpp5e Controls Ciliogenesis by Regulating Phosphoinositides at the Apical Membrane.
Journal of the American Society of Nephrology : JASN
Xu W,Jin M,Hu R,Wang H,Zhang F,Yuan S,Cao Y
Sun Jan 01 00:00:00 UTC 2017
The Joubert Syndrome Protein Inpp5e Controls Ciliogenesis by Regulating Phosphoinositides at the Apical Membrane.
Journal of the American Society of Nephrology : JASN
Xu W,Jin M,Hu R,Wang H,Zhang F,Yuan S,Cao Y
Sun Jan 01 00:00:00 UTC 2017
Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E.
Journal of cell science
Nozaki S,Katoh Y,Terada M,Michisaka S,Funabashi T,Takahashi S,Kontani K,Nakayama K
Wed Feb 01 00:00:00 UTC 2017
Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E.
Journal of cell science
Nozaki S,Katoh Y,Terada M,Michisaka S,Funabashi T,Takahashi S,Kontani K,Nakayama K
Wed Feb 01 00:00:00 UTC 2017
The guanine nucleotide exchange factor Arf-like protein 13b is essential for assembly of the mouse photoreceptor transition zone and outer segment.
The Journal of biological chemistry
Hanke-Gogokhia C,Wu Z,Sharif A,Yazigi H,Frederick JM,Baehr W
Fri Dec 29 00:00:00 UTC 2017
KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signalling.
Nature communications
Schou KB,Mogensen JB,Morthorst SK,Nielsen BS,Aleliunaite A,Serra-Marques A,Fürstenberg N,Saunier S,Bizet AA,Veland IR,Akhmanova A,Christensen ST,Pedersen LB
Mon Jan 30 00:00:00 UTC 2017
KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signalling.
Nature communications
Schou KB,Mogensen JB,Morthorst SK,Nielsen BS,Aleliunaite A,Serra-Marques A,Fürstenberg N,Saunier S,Bizet AA,Veland IR,Akhmanova A,Christensen ST,Pedersen LB
Mon Jan 30 00:00:00 UTC 2017
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.
PloS one
Goetz SC,Bangs F,Barrington CL,Katsanis N,Anderson KV
Fri Sep 08 00:00:00 UTC 2017
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.
PloS one
Goetz SC,Bangs F,Barrington CL,Katsanis N,Anderson KV
Fri Sep 08 00:00:00 UTC 2017
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
Journal of medical genetics
Slaats GG,Isabella CR,Kroes HY,Dempsey JC,Gremmels H,Monroe GR,Phelps IG,Duran KJ,Adkins J,Kumar SA,Knutzen DM,Knoers NV,Mendelsohn NJ,Neubauer D,Mastroyianni SD,Vogt J,Worgan L,Karp N,Bowdin S,Glass IA,Parisi MA,Otto EA,Johnson CA,Hildebrandt F,van Haaften G,Giles RH,Doherty D
Fri Jan 01 00:00:00 UTC 2016
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
Journal of medical genetics
Slaats GG,Isabella CR,Kroes HY,Dempsey JC,Gremmels H,Monroe GR,Phelps IG,Duran KJ,Adkins J,Kumar SA,Knutzen DM,Knoers NV,Mendelsohn NJ,Neubauer D,Mastroyianni SD,Vogt J,Worgan L,Karp N,Bowdin S,Glass IA,Parisi MA,Otto EA,Johnson CA,Hildebrandt F,van Haaften G,Giles RH,Doherty D
Fri Jan 01 00:00:00 UTC 2016
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
Journal of medical genetics
Slaats GG,Isabella CR,Kroes HY,Dempsey JC,Gremmels H,Monroe GR,Phelps IG,Duran KJ,Adkins J,Kumar SA,Knutzen DM,Knoers NV,Mendelsohn NJ,Neubauer D,Mastroyianni SD,Vogt J,Worgan L,Karp N,Bowdin S,Glass IA,Parisi MA,Otto EA,Johnson CA,Hildebrandt F,van Haaften G,Giles RH,Doherty D
Fri Jan 01 00:00:00 UTC 2016
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
Journal of medical genetics
Slaats GG,Isabella CR,Kroes HY,Dempsey JC,Gremmels H,Monroe GR,Phelps IG,Duran KJ,Adkins J,Kumar SA,Knutzen DM,Knoers NV,Mendelsohn NJ,Neubauer D,Mastroyianni SD,Vogt J,Worgan L,Karp N,Bowdin S,Glass IA,Parisi MA,Otto EA,Johnson CA,Hildebrandt F,van Haaften G,Giles RH,Doherty D
Fri Jan 01 00:00:00 UTC 2016
Inpp5e suppresses polycystic kidney disease via inhibition of PI3K/Akt-dependent mTORC1 signaling.
Human molecular genetics
Hakim S,Dyson JM,Feeney SJ,Davies EM,Sriratana A,Koenig MN,Plotnikova OV,Smyth IM,Ricardo SD,Hobbs RM,Mitchell CA
Wed Jun 01 00:00:00 UTC 2016
Inpp5e suppresses polycystic kidney disease via inhibition of PI3K/Akt-dependent mTORC1 signaling.
Human molecular genetics
Hakim S,Dyson JM,Feeney SJ,Davies EM,Sriratana A,Koenig MN,Plotnikova OV,Smyth IM,Ricardo SD,Hobbs RM,Mitchell CA
Wed Jun 01 00:00:00 UTC 2016
Role for the IFT-A Complex in Selective Transport to the Primary Cilium.
Cell reports
Fu W,Wang L,Kim S,Li J,Dynlacht BD
Tue Nov 01 00:00:00 UTC 2016
Role for the IFT-A Complex in Selective Transport to the Primary Cilium.
Cell reports
Fu W,Wang L,Kim S,Li J,Dynlacht BD
Tue Nov 01 00:00:00 UTC 2016
Phosphatidylinositol phosphate kinase PIPKIγ and phosphatase INPP5E coordinate initiation of ciliogenesis.
Nature communications
Xu Q,Zhang Y,Wei Q,Huang Y,Hu J,Ling K
Fri Feb 26 00:00:00 UTC 2016
Phosphatidylinositol phosphate kinase PIPKIγ and phosphatase INPP5E coordinate initiation of ciliogenesis.
Nature communications
Xu Q,Zhang Y,Wei Q,Huang Y,Hu J,Ling K
Fri Feb 26 00:00:00 UTC 2016
INPP5E interacts with AURKA, linking phosphoinositide signaling to primary cilium stability.
Journal of cell science
Plotnikova OV,Seo S,Cottle DL,Conduit S,Hakim S,Dyson JM,Mitchell CA,Smyth IM
Thu Jan 15 00:00:00 UTC 2015
INPP5E interacts with AURKA, linking phosphoinositide signaling to primary cilium stability.
Journal of cell science
Plotnikova OV,Seo S,Cottle DL,Conduit S,Hakim S,Dyson JM,Mitchell CA,Smyth IM
Thu Jan 15 00:00:00 UTC 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice.
Neurogenetics
Yang AW,Sachs AJ,Nystuen AM
Thu Oct 01 00:00:00 UTC 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice.
Neurogenetics
Yang AW,Sachs AJ,Nystuen AM
Thu Oct 01 00:00:00 UTC 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice.
Neurogenetics
Yang AW,Sachs AJ,Nystuen AM
Thu Oct 01 00:00:00 UTC 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice.
Neurogenetics
Yang AW,Sachs AJ,Nystuen AM
Thu Oct 01 00:00:00 UTC 2015
A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.
Human mutation
Thomas S,Wright KJ,Le Corre S,Micalizzi A,Romani M,Abhyankar A,Saada J,Perrault I,Amiel J,Litzler J,Filhol E,Elkhartoufi N,Kwong M,Casanova JL,Boddaert N,Baehr W,Lyonnet S,Munnich A,Burglen L,Chassaing N,Encha-Ravazi F,Vekemans M,Gleeson JG,Valente EM,Jackson PK,Drummond IA,Saunier S,Attié-Bitach T
Wed Jan 01 00:00:00 UTC 2014
A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.
Human mutation
Thomas S,Wright KJ,Le Corre S,Micalizzi A,Romani M,Abhyankar A,Saada J,Perrault I,Amiel J,Litzler J,Filhol E,Elkhartoufi N,Kwong M,Casanova JL,Boddaert N,Baehr W,Lyonnet S,Munnich A,Burglen L,Chassaing N,Encha-Ravazi F,Vekemans M,Gleeson JG,Valente EM,Jackson PK,Drummond IA,Saunier S,Attié-Bitach T
Wed Jan 01 00:00:00 UTC 2014
A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.
Human mutation
Thomas S,Wright KJ,Le Corre S,Micalizzi A,Romani M,Abhyankar A,Saada J,Perrault I,Amiel J,Litzler J,Filhol E,Elkhartoufi N,Kwong M,Casanova JL,Boddaert N,Baehr W,Lyonnet S,Munnich A,Burglen L,Chassaing N,Encha-Ravazi F,Vekemans M,Gleeson JG,Valente EM,Jackson PK,Drummond IA,Saunier S,Attié-Bitach T
Wed Jan 01 00:00:00 UTC 2014
A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.
Human mutation
Thomas S,Wright KJ,Le Corre S,Micalizzi A,Romani M,Abhyankar A,Saada J,Perrault I,Amiel J,Litzler J,Filhol E,Elkhartoufi N,Kwong M,Casanova JL,Boddaert N,Baehr W,Lyonnet S,Munnich A,Burglen L,Chassaing N,Encha-Ravazi F,Vekemans M,Gleeson JG,Valente EM,Jackson PK,Drummond IA,Saunier S,Attié-Bitach T
Wed Jan 01 00:00:00 UTC 2014
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting.
Proceedings of the National Academy of Sciences of the United States of America
Humbert MC,Weihbrecht K,Searby CC,Li Y,Pope RM,Sheffield VC,Seo S
Tue Nov 27 00:00:00 UTC 2012
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting.
Proceedings of the National Academy of Sciences of the United States of America
Humbert MC,Weihbrecht K,Searby CC,Li Y,Pope RM,Sheffield VC,Seo S
Tue Nov 27 00:00:00 UTC 2012
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting.
Proceedings of the National Academy of Sciences of the United States of America
Humbert MC,Weihbrecht K,Searby CC,Li Y,Pope RM,Sheffield VC,Seo S
Tue Nov 27 00:00:00 UTC 2012
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting.
Proceedings of the National Academy of Sciences of the United States of America
Humbert MC,Weihbrecht K,Searby CC,Li Y,Pope RM,Sheffield VC,Seo S
Tue Nov 27 00:00:00 UTC 2012
