PMC Links for GEO Profiles (Select 114144385) - PMC

Select item 49511961.

The Lamin B receptor is essential for cholesterol synthesis and perturbed by disease-causing mutations

Pei-Ling Tsai, Chenguang Zhao, Elizabeth Turner, Christian Schlieker

eLife. 2016; 5: e16011. Published online 2016 Jun 23. doi: 10.7554/eLife.16011

PMCID:: PMC4951196

Abstract Article PDF–5.7M

Select item 38309392.

Tudor: a versatile family of histone methylation ‘readers’

Rui Lu, Gang Greg Wang

Trends Biochem Sci. Author manuscript; available in PMC 2014 Nov 1.

Published in final edited form as: Trends Biochem Sci. 2013 Nov; 38(11): 10.1016/j.tibs.2013.08.002. Published online 2013 Sep 10. doi: 10.1016/j.tibs.2013.08.002

PMCID:: PMC3830939

Abstract Article PDF–945K

Select item 32445483.

Lamin B receptor (LBR) regulates the growth and maturation of myeloid progenitors via its sterol reductase domain: Implications for cholesterol biosynthesis in regulating myelopoiesis

Gayathri Subramanian, Pulkit Chaudhury, Krishnakumar Malu, Samantha Fowler, Rahul Manmode, Deepali Gotur, Monika Zwerger, David Ryan, Rita Roberti, Peter Gaines

J Immunol. Author manuscript; available in PMC 2013 Jan 1.

Published in final edited form as: J Immunol. 2012 Jan 1; 188(1): 85–102. Published online 2011 Dec 2. doi: 10.4049/jimmunol.1003804

PMCID:: PMC3244548

Abstract Article PDF–1.2M

Select item 31780594.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 30270445.

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein

Peter Clayton, Björn Fischer, Anuska Mann, Sahar Mansour, Eva Rossier, Markus Veen, Christine Lang, Sevjidmaa Baasanjav, Moritz Kieslich, Katja Brossuleit, Sophia Gravemann, Nele Schnipper, Mohsen Karbasyian, Ilja Demuth, Monika Zwerger, Amparo Vaya, Gerd Utermann, Stefan Mundlos, Sigmar Stricker, Karl Sperling, Katrin Hoffmann

Nucleus. 2010 Jul-Aug; 1(4): 354–366. Published online 2010 May 21. doi: 10.4161/nucl.1.4.12435

PMCID:: PMC3027044

Abstract Article PDF–3.5M

Select item 29068676.

A molecular mechanism underlying the neural-specific defect in torsinA mutant mice

Connie E. Kim, Alex Perez, Guy Perkins, Mark H. Ellisman, William T. Dauer

Proc Natl Acad Sci U S A. 2010 May 25; 107(21): 9861–9866. Published online 2010 May 10. doi: 10.1073/pnas.0912877107

PMCID:: PMC2906867

Abstract Article PDF–1.2M

Select item 11803307.

Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ¹⁴-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene

Hans R. Waterham, Janet Koster, Petra Mooyer, Gerard van Noort, Richard I. Kelley, William R. Wilcox, Ronald J. A. Wanders, Raoul C. M. Hennekam, Jan C. Oosterwijk

Am J Hum Genet. 2003 Apr; 72(4): 1013–1017. Published online 2003 Feb 28. doi: 10.1086/373938

PMCID:: PMC1180330

Abstract Article PDF–156K

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