A HomozygousNme7Mutation Is Associated withSitus Inversus Totalis

Laterality defects in the national birth defects prevention study (1998-2007): Birth prevalence and descriptive epidemiology

(2014) Angela E. Lin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

NME7 is a functional component of the γ-tubulin ring complex

(2014) Pengfei Liu et al.   MOLECULAR BIOLOGY OF THE CELL

Ectopic Expression of Human BBS4 Can Rescue Bardet-Biedl Syndrome Phenotypes in Bbs4 Null Mice

(2013) Xitiz Chamling et al.   PLoS One

High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

(2012) Nader Nakhleh et al.   CIRCULATION

Template-based protein structure modeling using the RaptorX web server

(2012) Morten Källberg et al.   Nature Protocols

Cilia at the Node of Mouse Embryos Sense Fluid Flow for Left-Right Determination via Pkd2

(2012) S. Yoshiba et al.   SCIENCE

A shRNA Functional Screen Reveals Nme6 and Nme7 Are Crucial for Embryonic Stem Cell Renewal

(2012) Chia-Hui Wang et al.   STEM CELLS

Functional characterization of putative cilia genes by high-content analysis

(2011) Cary K. Lai et al.   MOLECULAR BIOLOGY OF THE CELL

Congenital Hydrocephalus in Genetically Engineered Mice

(2011) P. Vogel et al.   VETERINARY PATHOLOGY

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

(2011) Muhammad Tariq et al.   GENOME BIOLOGY

NDP Kinase 7 Is a Conserved Microtubule-Binding Protein Preferentially Expressed in Ciliated Cells

(2010) Takashi Ikeda   CELL STRUCTURE AND FUNCTION

CDK5RAP2 stimulates microtubule nucleation by the γ-tubulin ring complex

(2010) Yuk-Kwan Choi et al.   JOURNAL OF CELL BIOLOGY

Systematic Analysis of Human Protein Complexes Identifies Chromosome Segregation Proteins

(2010) J. R. A. Hutchins et al.   SCIENCE

Situs Inversus in Dpcd/Poll–/–, Nme7–/–, and Pkd1l1–/– Mice

(2010) P. Vogel et al.   VETERINARY PATHOLOGY

Nme protein family evolutionary history, a vertebrate perspective

(2009) Thomas Desvignes et al.   BMC EVOLUTIONARY BIOLOGY

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

(2008) Bhagyalaxmi Mohapatra et al.   HUMAN MOLECULAR GENETICS