Product References
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.
Journal of medical genetics
Tian S,Tu C,He X,Meng L,Wang J,Tang S,Gao Y,Liu C,Wu H,Zhou Y,Lv M,Lin G,Jin L,Cao Y,Tang D,Zhang F,Tan YQ
Tue Aug 01 00:00:00 UTC 2023
The intraflagellar transport protein IFT52 associated with short-rib thoracic dysplasia is essential for ciliary function in osteogenic differentiation in vitro and for sensory perception in Drosophila.
Experimental cell research
Guleria VS,Parit R,Quadri N,Das R,Upadhyai P
Thu Sep 15 00:00:00 UTC 2022
KLC3 Regulates Ciliary Trafficking and Cyst Progression in CILK1 Deficiency-Related Polycystic Kidney Disease.
Journal of the American Society of Nephrology : JASN
Rah G,Cha H,Kim J,Song J,Kim H,Oh YK,Ahn C,Kang M,Kim J,Yoo KH,Kim MJ,Ko HW,Ko JY,Park JH
Thu Sep 01 00:00:00 UTC 2022
KLC3 Regulates Ciliary Trafficking and Cyst Progression in CILK1 Deficiency-Related Polycystic Kidney Disease.
Journal of the American Society of Nephrology : JASN
Rah G,Cha H,Kim J,Song J,Kim H,Oh YK,Ahn C,Kang M,Kim J,Yoo KH,Kim MJ,Ko HW,Ko JY,Park JH
Thu Sep 01 00:00:00 UTC 2022
KLC3 Regulates Ciliary Trafficking and Cyst Progression in CILK1 Deficiency-Related Polycystic Kidney Disease.
Journal of the American Society of Nephrology : JASN
Rah G,Cha H,Kim J,Song J,Kim H,Oh YK,Ahn C,Kang M,Kim J,Yoo KH,Kim MJ,Ko HW,Ko JY,Park JH
Thu Sep 01 00:00:00 UTC 2022
KLC3 Regulates Ciliary Trafficking and Cyst Progression in CILK1 Deficiency-Related Polycystic Kidney Disease.
Journal of the American Society of Nephrology : JASN
Rah G,Cha H,Kim J,Song J,Kim H,Oh YK,Ahn C,Kang M,Kim J,Yoo KH,Kim MJ,Ko HW,Ko JY,Park JH
Thu Sep 01 00:00:00 UTC 2022
Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.
Journal of medical genetics
Cong J,Wang X,Amiri-Yekta A,Wang L,Kherraf ZE,Liu C,Cazin C,Tang S,Hosseini SH,Tian S,Daneshipour A,Wang J,Zhou Y,Zeng Y,Yang S,He X,Li J,Cao Y,Jin L,Ray PF,Zhang F
Fri Jul 01 00:00:00 UTC 2022
Rabl2 GTP hydrolysis licenses BBSome-mediated export to fine-tune ciliary signaling.
The EMBO journal
Duan S,Li H,Zhang Y,Yang S,Chen Y,Qiu B,Huang C,Wang J,Li J,Zhu X,Yan X
Fri Jan 15 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
IFT proteins interact with HSET to promote supernumerary centrosome clustering in mitosis.
EMBO reports
Vitre B,Taulet N,Guesdon A,Douanier A,Dosdane A,Cisneros M,Maurin J,Hettinger S,Anguille C,Taschner M,Lorentzen E,Delaval B
Thu Jun 04 00:00:00 UTC 2020
IFT proteins interact with HSET to promote supernumerary centrosome clustering in mitosis.
EMBO reports
Vitre B,Taulet N,Guesdon A,Douanier A,Dosdane A,Cisneros M,Maurin J,Hettinger S,Anguille C,Taschner M,Lorentzen E,Delaval B
Thu Jun 04 00:00:00 UTC 2020
Vertebrate Dynein-f depends on Wdr78 for axonemal localization and is essential for ciliary beat.
Journal of molecular cell biology
Zhang Y,Chen Y,Zheng J,Wang J,Duan S,Zhang W,Yan X,Zhu X
Wed May 01 00:00:00 UTC 2019
Vertebrate Dynein-f depends on Wdr78 for axonemal localization and is essential for ciliary beat.
Journal of molecular cell biology
Zhang Y,Chen Y,Zheng J,Wang J,Duan S,Zhang W,Yan X,Zhu X
Wed May 01 00:00:00 UTC 2019
Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.
Human molecular genetics
Dupont MA,Humbert C,Huber C,Siour Q,Guerrera IC,Jung V,Christensen A,Pouliet A,Garfa-Traoré M,Nitschké P,Injeyan M,Millar K,Chitayat D,Shannon P,Girisha KM,Shukla A,Mechler C,Lorentzen E,Benmerah A,Cormier-Daire V,Jeanpierre C,Saunier S,Delous M
Thu Aug 15 00:00:00 UTC 2019
Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.
Human molecular genetics
Dupont MA,Humbert C,Huber C,Siour Q,Guerrera IC,Jung V,Christensen A,Pouliet A,Garfa-Traoré M,Nitschké P,Injeyan M,Millar K,Chitayat D,Shannon P,Girisha KM,Shukla A,Mechler C,Lorentzen E,Benmerah A,Cormier-Daire V,Jeanpierre C,Saunier S,Delous M
Thu Aug 15 00:00:00 UTC 2019
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice.
American journal of human genetics
Liu C,He X,Liu W,Yang S,Wang L,Li W,Wu H,Tang S,Ni X,Wang J,Gao Y,Tian S,Zhang L,Cong J,Zhang Z,Tan Q,Zhang J,Li H,Zhong Y,Lv M,Li J,Jin L,Cao Y,Zhang F
Thu Dec 05 00:00:00 UTC 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.
American journal of human genetics
Liu W,He X,Yang S,Zouari R,Wang J,Wu H,Kherraf ZE,Liu C,Coutton C,Zhao R,Tang D,Tang S,Lv M,Fang Y,Li W,Li H,Zhao J,Wang X,Zhao S,Zhang J,Arnoult C,Jin L,Zhang Z,Ray PF,Cao Y,Zhang F
Thu Apr 04 00:00:00 UTC 2019
FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia.
Proceedings of the National Academy of Sciences of the United States of America
Honda A,Kita T,Seshadri SV,Misaki K,Ahmed Z,Ladbury JE,Richardson GP,Yonemura S,Ladher RK
Tue Aug 14 00:00:00 UTC 2018
FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia.
Proceedings of the National Academy of Sciences of the United States of America
Honda A,Kita T,Seshadri SV,Misaki K,Ahmed Z,Ladbury JE,Richardson GP,Yonemura S,Ladher RK
Tue Aug 14 00:00:00 UTC 2018
Robust interaction of IFT70 with IFT52-IFT88 in the IFT-B complex is required for ciliogenesis.
Biology open
Takei R,Katoh Y,Nakayama K
Mon Apr 30 00:00:00 UTC 2018
Robust interaction of IFT70 with IFT52-IFT88 in the IFT-B complex is required for ciliogenesis.
Biology open
Takei R,Katoh Y,Nakayama K
Mon Apr 30 00:00:00 UTC 2018
Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells.
Scientific reports
Silva LM,Jacobs DT,Allard BA,Fields TA,Sharma M,Wallace DP,Tran PV
Wed Mar 21 00:00:00 UTC 2018
Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells.
Scientific reports
Silva LM,Jacobs DT,Allard BA,Fields TA,Sharma M,Wallace DP,Tran PV
Wed Mar 21 00:00:00 UTC 2018
IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning.
Nature communications
Taulet N,Vitre B,Anguille C,Douanier A,Rocancourt M,Taschner M,Lorentzen E,Echard A,Delaval B
Mon Dec 04 00:00:00 UTC 2017
IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning.
Nature communications
Taulet N,Vitre B,Anguille C,Douanier A,Rocancourt M,Taschner M,Lorentzen E,Echard A,Delaval B
Mon Dec 04 00:00:00 UTC 2017
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome.
Human molecular genetics
Zhang W,Taylor SP,Nevarez L,Lachman RS,Nickerson DA,Bamshad M,Krakow D,Cohn DH
Thu Sep 15 00:00:00 UTC 2016
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
Scientific reports
Duran I,Taylor SP,Zhang W,Martin J,Forlenza KN,Spiro RP,Nickerson DA,Bamshad M,Cohn DH,Krakow D
Mon Sep 26 00:00:00 UTC 2016
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
Scientific reports
Duran I,Taylor SP,Zhang W,Martin J,Forlenza KN,Spiro RP,Nickerson DA,Bamshad M,Cohn DH,Krakow D
Mon Sep 26 00:00:00 UTC 2016
Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function.
PloS one
Xu Y,Cao J,Huang S,Feng D,Zhang W,Zhu X,Yan X
Mon Apr 18 00:00:00 UTC 2016
Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function.
PloS one
Xu Y,Cao J,Huang S,Feng D,Zhang W,Zhu X,Yan X
Mon Apr 18 00:00:00 UTC 2016
Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.
PLoS genetics
Cevik S,Sanders AA,Van Wijk E,Boldt K,Clarke L,van Reeuwijk J,Hori Y,Horn N,Hetterschijt L,Wdowicz A,Mullins A,Kida K,Kaplan OI,van Beersum SE,Man Wu K,Letteboer SJ,Mans DA,Katada T,Kontani K,Ueffing M,Roepman R,Kremer H,Blacque OE
Wed Aug 20 00:00:00 UTC 2014
Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.
PLoS genetics
Cevik S,Sanders AA,Van Wijk E,Boldt K,Clarke L,van Reeuwijk J,Hori Y,Horn N,Hetterschijt L,Wdowicz A,Mullins A,Kida K,Kaplan OI,van Beersum SE,Man Wu K,Letteboer SJ,Mans DA,Katada T,Kontani K,Ueffing M,Roepman R,Kremer H,Blacque OE
Wed Aug 20 00:00:00 UTC 2014
The cilia protein IFT88 is required for spindle orientation in mitosis.
Nature cell biology
Delaval B,Bright A,Lawson ND,Doxsey S
Fri Apr 01 00:00:00 UTC 2011
The cilia protein IFT88 is required for spindle orientation in mitosis.
Nature cell biology
Delaval B,Bright A,Lawson ND,Doxsey S
Fri Apr 01 00:00:00 UTC 2011
