4.8 Article

Evolutionarily Assembled cis-Regulatory Module at a Human Ciliopathy Locus

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Cell Biology

Trafficking to the Ciliary Membrane: How to Get Across the Periciliary Diffusion Barrier?

Maxence V. Nachury et al.

ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 26 (2010)

Article Genetics & Heredity

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

Enza Maria Valente et al.

NATURE GENETICS (2010)

Review Genetics & Heredity

The nonmotile ciliopathies

Jonathan L. Tobin et al.

GENETICS IN MEDICINE (2009)

Article Genetics & Heredity

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

Hemant Khanna et al.

NATURE GENETICS (2009)

Review Cell Biology

A systems biology approach to understanding cis-regulatory module function

Danuta M. Jeziorska et al.

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2009)

Review Clinical Neurology

Joubert Syndrome: Insights Into Brain Development, Cilium Biology, and Complex Disease

Dan Doherty

SEMINARS IN PEDIATRIC NEUROLOGY (2009)

Article Cell Biology

The zebrafish fleer gene encodes an essential regulator of cilia tubulin polyglutamylation

Narendra Pathak et al.

MOLECULAR BIOLOGY OF THE CELL (2007)

Review Multidisciplinary Sciences

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

Veena Singla et al.

SCIENCE (2006)

Review Genetics & Heredity

The evolutionary dynamics of eukaryotic gene order

LD Hurst et al.

NATURE REVIEWS GENETICS (2004)

Article Multidisciplinary Sciences

A gene-coexpression network for global discovery of conserved genetic modules

JM Stuart et al.

SCIENCE (2003)

Article Genetics & Heredity

Description, nomenclature, and mapping of a novel cerebello-renal syndrome with the molar tooth malformation

EM Valente et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Genetics & Heredity

Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome

VL Ruiz-Perez et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)