[HTML][HTML] A unified model for left–right asymmetry? Comparison and synthesis of molecular models of embryonic laterality

LN Vandenberg, M Levin - Developmental biology, 2013 - Elsevier
Understanding how and when the left–right (LR) axis is first established is a fundamental
question in developmental biology. A popular model is that the LR axis is established …

Right, left and cilia: How asymmetry is established

RB Little, DP Norris - Seminars in Cell & Developmental Biology, 2021 - Elsevier
The initial breaking of left-right (L–R) symmetry in the embryo is controlled by a motile-cilia-
driven leftward fluid flow in the left-right organiser (LRO), resulting in L–R asymmetric gene …

Cilia at the node of mouse embryos sense fluid flow for left-right determination via Pkd2

S Yoshiba, H Shiratori, IY Kuo, A Kawasumi… - Science, 2012 - science.org
Unidirectional fluid flow plays an essential role in the breaking of left-right (LR) symmetry in
mouse embryos, but it has remained unclear how the flow is sensed by the embryo. We …

Pkd1l1 establishes left-right asymmetry and physically interacts with Pkd2

S Field, KL Riley, DT Grimes, H Hilton… - …, 2011 - journals.biologists.com
In mammals, left-right (LR) asymmetry is established by posteriorly oriented cilia driving a
leftwards laminar flow in the embryonic node, thereby activating asymmetric gene …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - nature.com
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Current insights into renal ciliopathies: what can genetics teach us?

HH Arts, NVAM Knoers - Pediatric nephrology, 2013 - Springer
Ciliopathies are a group of clinically and genetically overlapping disorders whose etiologies
lie in defective cilia. These are antenna-like organelles on the apical surface of numerous …

Mouse models of ciliopathies: the state of the art

DP Norris, DT Grimes - Disease models & mechanisms, 2012 - journals.biologists.com
The ciliopathies are an apparently disparate group of human diseases that all result from
defects in the formation and/or function of cilia. They include disorders such as Meckel …

[HTML][HTML] Symmetry breakage in the vertebrate embryo: when does it happen and how does it work?

M Blum, A Schweickert, P Vick, CVE Wright… - Developmental …, 2014 - Elsevier
Asymmetric development of the vertebrate embryo has fascinated embryologists for over a
century. Much has been learned since the asymmetric Nodal signaling cascade in the left …

Trafficking to the primary cilium membrane

S Mukhopadhyay, HB Badgandi, S Hwang… - Molecular biology of …, 2017 - Am Soc Cell Biol
The primary cilium has been found to be associated with a number of cellular signaling
pathways, such as vertebrate hedgehog signaling, and implicated in the pathogenesis of …

Motile cilia genetics and cell biology: big results from little mice

L Lee, LE Ostrowski - Cellular and Molecular Life Sciences, 2021 - Springer
Our understanding of motile cilia and their role in disease has increased tremendously over
the last two decades, with critical information and insight coming from the analysis of mouse …