User profiles for J. F. Reiter

Jeremy Reiter

Chair, Dept of Biochemistry, University of California, San Francisco
Verified email at ucsf.edu
Cited by 16037

The primary cilium as the cell's antenna: signaling at a sensory organelle

V Singla, JF Reiter - science, 2006 - science.org
Almost every vertebrate cell has a specialized cell surface projection called a primary cilium.
Although these structures were first described more than a century ago, the full scope of …

Genes and molecular pathways underpinning ciliopathies

JF Reiter, MR Leroux - Nature reviews Molecular cell biology, 2017 - nature.com
Motile and non-motile (primary) cilia are nearly ubiquitous cellular organelles. The dysfunction
of cilia causes diseases known as ciliopathies. The number of reported ciliopathies (…

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

JF Reiter, OE Blacque, MR Leroux - EMBO reports, 2012 - embopress.org
Both the basal body and the microtubule‐based axoneme it nucleates have evolutionarily
conserved subdomains crucial for cilium biogenesis, function and maintenance. Here, we …

Vertebrate Smoothened functions at the primary cilium

…, V Singla, AR Norman, DYR Stainier, JF Reiter - Nature, 2005 - nature.com
The unanticipated involvement of several intraflagellar transport proteins in the mammalian
Hedgehog (Hh) pathway has hinted at a functional connection between cilia and Hh signal …

[HTML][HTML] Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

…, JB Vincent, DA Doherty, F Hildebrandt, JF Reiter… - Cell, 2011 - cell.com
Nephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are
autosomal-recessive ciliopathies presenting with cystic kidneys, retinal degeneration, and …

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

…, N Katsanis, F Hildebrandt, JF Reiter - Nature …, 2011 - nature.com
Mutations affecting ciliary components cause ciliopathies. As described here, we investigated
Tectonic1 (Tctn1), a regulator of mouse Hedgehog signaling, and found that it is essential …

Kif3a constrains β-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms

…, WE Dowdle, J Gaulden, V Singla, JF Reiter - Nature cell …, 2008 - nature.com
… Cheyette, and members of the Reiter lab for helpful discussions. Support for microscopy
was provided by the NIH (P30 DK063720). This work was supported by funding from the NSF (…

Primary cilia can both mediate and suppress Hedgehog pathway–dependent tumorigenesis

…, CK Bichakjian, EH Epstein Jr, AA Dlugosz, JF Reiter - Nature medicine, 2009 - nature.com
… Evan and the members of the Reiter lab for critical reading of this manuscript; K. Thorn and
the UCSF Nikon Imaging Center for assistance with confocal microscopy; C. Miller and JD …

Gata5 is required for the development of the heart and endoderm in zebrafish

JF Reiter, J Alexander, A Rodaway… - Genes & …, 1999 - genesdev.cshlp.org
The mechanisms regulating vertebrate heart and endoderm development have recently
become the focus of intense study. Here we present evidence from both loss- and gain-of-…

[HTML][HTML] Cell-type-specific alternative splicing governs cell fate in the developing cerebral cortex

…, J Fan, R Doan, M Ozawa, J Ma, N Yoshida, JF Reiter… - Cell, 2016 - cell.com
Alternative splicing is prevalent in the mammalian brain. To interrogate the functional role of
alternative splicing in neural development, we analyzed purified neural progenitor cells (…