N. Klena

发表

Global genetic analysis in mice unveils central role for cilia in congenital heart disease

Janan T. Eppig, Madhavi K. Ganapathiraju, Mohamed Thahir, 2015, Nature.

Architecture of the centriole cartwheel‐containing region revealed by cryo‐electron tomography

Philipp S. Erdmann, H. Stahlberg, B. Engel, 2020, The EMBO journal.

Overview of the centriole architecture.

N. Klena, P. Guichard, V. Hamel, 2020, Current opinion in structural biology.

Isolation and Fluorescence Imaging for Single-particle Reconstruction of Chlamydomonas Centrioles

N. Klena, P. Guichard, V. Hamel, 2018, Journal of visualized experiments : JoVE.

Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families

Morad Ansari, Alejandro Sifrim, Matthew E Hurles, 2015, Nature Genetics.

CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation

H. Omran, S. Letteboer, R. Roepman, 2014, American journal of human genetics.

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Nathan A. Bihlmeyer, Henry J. Lin, Blair H. Smith, 2018, Genome Biology.

Genetic link between renal birth defects and congenital heart disease

A. Panigrahy, G. Pazour, N. Klena, 2016, Nature Communications.

Cilia and Ciliopathies in Congenital Heart Disease.

N. Klena, C. Lo, Brian C. Gibbs, 2017, Cold Spring Harbor perspectives in biology.

Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.

G. Pazour, You Li, N. Klena, 2014, Birth defects research. Part C, Embryo today : reviews.

Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia

A. Panigrahy, You Li, N. Klena, 2015, American journal of medical genetics. Part A.

Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.

K. Chu, G. Tearney, S. Birket, 2017, JCI insight.

The architecture of the centriole cartwheel-containing region revealed by cryo-electron tomography

Philipp S. Erdmann, H. Stahlberg, B. Engel, 2020, bioRxiv.

The complex genetics of hypoplastic left heart syndrome

Simon Watkins, Michael Tsang, Paul Grossfeld, 2017, Nature Genetics.

Role of Cilia and Left-Right Patterning in Congenital Heart Disease

L. Leatherbury, G. Pazour, You Li, 2016 .

In situ architecture of the ciliary base reveals the stepwise assembly of intraflagellar transport trains

W. Baumeister, J. Plitzko, W. Wan, 2022, Science.

Kinesin-1 activity recorded in living cells with a precipitating dye

N. Klena, N. Winssinger, Christopher K. E. Bleck, 2021, Nature Communications.

Kinesin-1 motility traced by an activity-based precipitating dye

N. Klena, N. Winssinger, Christopher K. E. Bleck, 2020, bioRxiv.

Primary Cilia and Mammalian Hedgehog Signaling

Jan F. Jikeli, J. Reiter, Elizabeth N Schock, 2016 .

Cyclic Di-GMP Phosphodiesterases RmdA and RmdB Are Involved in Regulating Colony Morphology and Development in Streptomyces coelicolor

Jennifer A. Bennett, N. Klena, J. A. Bennett, 2012, Journal of bacteriology.

CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation

H. Omran, S. Letteboer, R. Roepman, 2014, American Journal of Human Genetics.

MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates

Laurie D. Smith, Neil A. Miller, Carol J. Saunders, 2015, Nature Genetics.

Visualizing the native cellular organization by coupling cryofixation with expansion microscopy (Cryo-ExM)

N. Klena, P. Guichard, V. Hamel, 2022, Nature Methods.

ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

Danielle K. Manning, W. Goessling, G. Pazour, 2015, Nature Communications.

Erratum: Genetic link between renal birth defects and congenital heart disease

A. Panigrahy, G. Pazour, N. Klena, 2016, Nature Communications.

Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2020, Frontiers in Physiology.

A helical inner scaffold provides a structural basis for centriole cohesion

Philipp S. Erdmann, H. Stahlberg, M. Bornens, 2020, Science Advances.

Lack of CCDC 146 , a ubiquitous centriole and microtubule-associated protein , 2 leads to non-syndromic male infertility in human and mouse 3 4 5

N. Thierry-Mieg, S. Geimer, P. Ray, 2023 .

Structural Biology of Cilia and Intraflagellar Transport.

N. Klena, G. Pigino, 2022, Annual review of cell and developmental biology.

Molecular Pathways and Animal Models of Defects of Situs

N. Klena, George C Gabriel, C. Lo, 2016 .

The Tubulin Nano-Code: a protofilament-specific pattern of tubulin post-translational modifications regulates ciliary beating mechanics

N. Klena, F. Martino, G. Pigino, 2023, bioRxiv.

In situ architecture of the ciliary base reveals the stepwise assembly of IFT trains

Philipp S. Erdmann, W. Baumeister, J. Plitzko, 2021, bioRxiv.

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Henry J. Lin, Blair H. Smith, M. Waldenberger, 2018, Genome Biology.

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

S. Geimer, P. Ray, N. Klena, 2023, bioRxiv.