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Summary Anatomy Item Literature (4906) Expression Attributions Wiki
XB-ANAT-3713

Papers associated with left (and tuba4b)

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Syndecan4 coordinates Wnt/JNK and BMP signaling to regulate foregut progenitor development., Zhang Z, Zhang Z., Dev Biol. August 1, 2016; 416 (1): 187-199.                                  

Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.                        

The sequential activation of the mitotic microtubule assembly pathways favors bipolar spindle formation., Cavazza T., Mol Biol Cell. October 1, 2016; 27 (19): 2935-45.                    

Foxn4 promotes gene expression required for the formation of multiple motile cilia., Campbell EP., Development. December 15, 2016; 143 (24): 4654-4664.                                  

What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia., Walentek P., Genesis. January 1, 2017; 55 (1-2):       

La-related protein 6 controls ciliated cell differentiation., Manojlovic Z., Cilia. January 1, 2017; 6 4.                

RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells., Sedzinski J., J Cell Sci. January 15, 2017; 130 (2): 420-428.                

Stomach curvature is generated by left-right asymmetric gut morphogenesis., Davis A., Development. April 15, 2017; 144 (8): 1477-1483.                      

The High-Affinity Interaction between ORC and DNA that Is Required for Replication Licensing Is Inhibited by 2-Arylquinolin-4-Amines., Gardner NJ., Cell Chem Biol. August 17, 2017; 24 (8): 981-992.e4.                        

hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus., Prager A., Dev Biol. October 1, 2017; 430 (1): 188-201.                      

Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling Pathways., Sigg MA., Dev Cell. December 18, 2017; 43 (6): 744-762.e11.      

Candidate Heterotaxy Gene FGFR4 Is Essential for Patterning of the Left-Right Organizer in Xenopus., Sempou E., Front Physiol. January 1, 2018; 9 1705.              

A Conserved Role of the Unconventional Myosin 1d in Laterality Determination., Tingler M., Curr Biol. March 5, 2018; 28 (5): 810-816.e3.                

Three-dimensional reconstruction of the cranial and anterior spinal nerves in early tadpoles of Xenopus laevis (Pipidae, Anura)., Naumann B., J Comp Neurol. April 1, 2018; 526 (5): 836-857.                      

WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation., Kulkarni SS., Dev Cell. September 10, 2018; 46 (5): 595-610.e3.                              

Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos., Willsey HR., Dev Biol. October 15, 2018; 442 (2): 276-287.                                      

CDC20B is required for deuterosome-mediated centriole production in multiciliated cells., Revinski DR., Nat Commun. November 7, 2018; 9 (1): 4668.              

WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS., Development. November 28, 2018; 145 (23):                 

A liquid-like organelle at the root of motile ciliopathy., Huizar RL., Elife. December 18, 2018; 7                               

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1., Ott T., Front Physiol. January 1, 2019; 10 134.                

Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo., Bharathan NK., Dev Biol. June 15, 2019; 450 (2): 115-131.                            

The role of sensory innervation in cornea-lens regeneration., Perry KJ., Dev Dyn. July 1, 2019; 248 (7): 530-544.          

The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos., Willsey HR., Development. June 22, 2020; 147 (21):                             

Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.                                                    

Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.          

Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):                                     

INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex., Mascibroda LG., Nat Commun. October 13, 2022; 13 (1): 6054.                    

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