[HTML][HTML] Signaling through the primary cilium
G Wheway, L Nazlamova, JT Hancock - Frontiers in cell and …, 2018 - frontiersin.org
The presence of single, non-motile “primary” cilia on the surface of epithelial cells has been
well described since the 1960s. However, for decades these organelles were believed to be …
well described since the 1960s. However, for decades these organelles were believed to be …
Neural progenitors, neurogenesis and the evolution of the neocortex
M Florio, WB Huttner - Development, 2014 - journals.biologists.com
The neocortex is the seat of higher cognitive functions and, in evolutionary terms, is the
youngest part of the mammalian brain. Since its origin, the neocortex has expanded in …
youngest part of the mammalian brain. Since its origin, the neocortex has expanded in …
The cilium: cellular antenna and central processing unit
JJ Malicki, CA Johnson - Trends in cell biology, 2017 - cell.com
Cilia mediate an astonishing diversity of processes. Recent advances provide unexpected
insights into the regulatory mechanisms of cilium formation, and reveal diverse regulatory …
insights into the regulatory mechanisms of cilium formation, and reveal diverse regulatory …
The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization
Both the basal body and the microtubule‐based axoneme it nucleates have evolutionarily
conserved subdomains crucial for cilium biogenesis, function and maintenance. Here, we …
conserved subdomains crucial for cilium biogenesis, function and maintenance. Here, we …
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
FR Garcia-Gonzalo, KC Corbit, MS Sirerol-Piquer… - 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 …
investigated Tectonic1 (Tctn1), a regulator of mouse Hedgehog signaling, and found that it is …
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling
CV Logan, G Szabadkai, JA Sharpe, DA Parry… - Nature …, 2014 - nature.com
Mitochondrial Ca2+ uptake has key roles in cell life and death. Physiological Ca2+ signaling
regulates aerobic metabolism, whereas pathological Ca2+ overload triggers cell death …
regulates aerobic metabolism, whereas pathological Ca2+ overload triggers cell death …
The molecular basis of human retinal and vitreoretinal diseases
W Berger, B Kloeckener-Gruissem… - Progress in retinal and eye …, 2010 - Elsevier
During the last two to three decades, a large body of work has revealed the molecular basis
of many human disorders, including retinal and vitreoretinal degenerations and …
of many human disorders, including retinal and vitreoretinal degenerations and …
[HTML][HTML] Evolution: Tracing the origins of centrioles, cilia, and flagella
Z Carvalho-Santos, J Azimzadeh… - The Journal of cell …, 2011 - ncbi.nlm.nih.gov
Centrioles/basal bodies (CBBs) are microtubule-based cylindrical organelles that nucleate
the formation of centrosomes, cilia, and flagella. CBBs, cilia, and flagella are ancestral …
the formation of centrosomes, cilia, and flagella. CBBs, cilia, and flagella are ancestral …
[HTML][HTML] Centrioles, centrosomes, and cilia in health and disease
Centrioles are barrel-shaped structures that are essential for the formation of centrosomes,
cilia, and flagella. Here we review recent advances in our understanding of the function and …
cilia, and flagella. Here we review recent advances in our understanding of the function and …
MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis
CL Williams, C Li, K Kida, PN Inglis, S Mohan… - Journal of Cell …, 2011 - rupress.org
Meckel-Gruber syndrome (MKS), nephronophthisis (NPHP), and related ciliopathies present
with overlapping phenotypes and display considerable allelism between at least twelve …
with overlapping phenotypes and display considerable allelism between at least twelve …