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Mechanisms and pathways of growth failure in primordial dwarfism.

author

Andrew Jackson

published in: Genes & Development

date of publication: 2011-10-01

Cites articles 133

Date

Title

Authors

2011-06

The Ras-ERK and PI3K-mTOR pathways: cross-talk and compensation
2011-04-22

Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size
2011-04-08

Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA

Annick Toutain, Françoise Clerget-Darpoux, Carol Wise, Siren Berland, Anne-Louise Leutenegger, Michael B Bober, Damien Sanlaville, Patrick Edery, Audrey Labalme
2011-04-08

Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD I

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2011-06

Mechanisms limiting body growth in mammals
2011-02-01

IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development

Salah Azzi
2011-03-03

Two sides of lifespan regulating genes: pro-longevity or anti-longevity?
2011-02-27

Mutations in the pre-replication complex cause Meier-Gorlin syndrome

Annick Toutain, Michael B Bober, Hans Van Bokhoven, John Dean, Karen Temple, Carol Wise, Andrew Jackson, John Marius Opitz, Louise Bicknell, Nine V. A. M. Knoers, Lies H. Hoefsloot
2011-01-26

Genetic defects in human pericentrin are associated with severe insulin resistance and diabetes

Robert K Semple, Mark O'Driscoll, Michael B Bober, Anna Krook, Isabel Huang-Doran, Andrew Jackson, Stephen O'Rahilly, Louise Bicknell
2011-01

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

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2011-05-31

Nuclear Chk1 prevents premature mitotic entry

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2011-02-01

The shortest of the short: pericentrin mutations and beyond

Anita Rauch
2011-02-27

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome

Carol Wise, Sarah Walker, Mark O'Driscoll, Michael B Bober, Louise Bicknell
2011-02-27

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.

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2010-12-01

A comprehensive map of the mTOR signaling network

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2010-12-01

Asymmetric cell division: recent developments and their implications for tumour biology

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2010-10-19

The hippo signaling pathway in development and cancer
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Gene expression profiling of U12-type spliceosome mutant Drosophila reveals widespread changes in metabolic pathways

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2010-10-01

Exon junction complex subunits are required to splice Drosophila MAP kinase, a large heterochromatic gene

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WDR62 is associated with the spindle pole and is mutated in human microcephaly

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dMyc functions downstream of Yorkie to promote the supercompetitive behavior of hippo pathway mutant cells

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

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2010-09-07

Arms and the man: the problem of symmetric growth
2010-09-09

Incremental genetic perturbations to MCM2-7 expression and subcellular distribution reveal exquisite sensitivity of mice to DNA replication stress
2010-07-01

Upstream regulation of the hippo size control pathway

Helena E. Richardson, Kieran Harvey
2010-07-01

Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

Jacques L. Michaud, Andrea L Rideout
2010-06

Novel CENPJ mutation causes Seckel syndrome

Fowzan S Alkuraya, Ranad Shaheen
2010-04-20

The Hippo pathway regulates Wnt/beta-catenin signaling

Anthony Pawson, Xaralabos Varelas, Walter Hunziker, Alex Gregorieff, Jeffrey L. Wrana
2010-04-04

The exon junction complex component Magoh controls brain size by regulating neural stem cell division

Dawn E Watkins-Chow, Karisa C. Schreck, Hungjiun Liaw, William J Pavan, Debra L Silver, Denise M Larson
2010-01-26

Mammalian Mst1 and Mst2 kinases play essential roles in organ size control and tumor suppression
2010-12-20

Chk1 inhibits replication factory activation but allows dormant origin firing in existing factories

J. Julian Blow
2010-12-01

Hippo signaling at a glance

Article - wd:Q37943258

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