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Select item 73112321.

A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome.

Steven D. Funk, Raymond H. Bayer, Karen K. McKee, Kazushi Okada, Hiroshi Nishimune, Peter D. Yurchenco, Jeffrey H. Miner

Kidney Int. Author manuscript; available in PMC 2021 Jul 1.

Published in final edited form as: Kidney Int. 2020 Jul; 98(1): 133–146. Published online 2020 Feb 20. doi: 10.1016/j.kint.2020.01.033

PMCID:: PMC7311232

Abstract Article PDF–4.1M

Select item 67829412.

Disruption of Laminin β2 Chain Production Causes Alterations in Morphology and Function in the CNS

Richard T. Libby, Christopher R. Lavallee, Grant W. Balkema, William J. Brunken, Dale D. Hunter

J Neurosci. 1999 Nov 1; 19(21): 9399–9411. doi: 10.1523/JNEUROSCI.19-21-09399.1999

PMCID:: PMC6782941

Abstract Article PDF–1.3M

Select item 45186913.

Albumin-associated free fatty acids induce macropinocytosis in podocytes

Jun-Jae Chung, Tobias B. Huber, Markus Gödel, George Jarad, Björn Hartleben, Christopher Kwoh, Alexander Keil, Aleksey Karpitskiy, Jiancheng Hu, Christine J. Huh, Marina Cella, Richard W. Gross, Jeffrey H. Miner, Andrey S. Shaw

J Clin Invest. 2015 Jun 1; 125(6): 2307–2316. Published online 2015 Apr 27. doi: 10.1172/JCI79641

PMCID:: PMC4518691

Abstract Article PDF–3.1M

Select item 42930664.

Loss of β2-laminin alters calcium sensitivity and voltage-gated calcium channel maturation of neurotransmission at the neuromuscular junction

Kirat K Chand, Kah Meng Lee, Mitja P Schenning, Nickolas A Lavidis, Peter G Noakes

J Physiol. 2015 Jan 1; 593(Pt 1): 245–265. Published online 2014 Dec 1. doi: 10.1113/jphysiol.2014.284133

PMCID:: PMC4293066

Abstract Article PDF–1.2M

Select item 42410315.

Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson’s syndrome

Katherine R Bull, Thomas Mason, Andrew J Rimmer, Tanya L Crockford, Karlee L Silver, Tiphaine Bouriez-Jones, Tertius A Hough, Shirine Chaudhry, Ian SD Roberts, Christopher C Goodnow, Richard J Cornall

J Pathol. 2013 May; 233(1): 18–26. Published online 2014 Feb 6. doi: 10.1002/path.4308

PMCID:: PMC4241031

Abstract Article PDF–4.0M

Select item 37367186.

Laminin β2 Gene Missense Mutation Produces Endoplasmic Reticulum Stress in Podocytes

Ying Maggie Chen, Yuefang Zhou, Gloriosa Go, Joseph T. Marmerstein, Yamato Kikkawa, Jeffrey H. Miner

J Am Soc Nephrol. 2013 Jul 31; 24(8): 1223–1233. Published online 2013 May 30. doi: 10.1681/ASN.2012121149

PMCID:: PMC3736718

Abstract Article

Select item 23425807.

Functional analysis of neurotransmission at β2-laminin deficient terminals

David Knight, Lynn K Tolley, David K Kim, Nick A Lavidis, Peter G Noakes

J Physiol. 2003 Feb 1; 546(Pt 3): 789–800. Published online 2002 Dec 20. doi: 10.1113/jphysiol.2002.030924

PMCID:: PMC2342580

Abstract Article PDF–496K

Select item 13637298.

Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: Implications for Pierson syndrome

Jeffrey H. Miner, Gloriosa Go, Jeanette Cunningham, Bruce L. Patton, George Jarad

Development. Author manuscript; available in PMC 2006 Sep 1.

Published in final edited form as: Development. 2006 Mar; 133(5): 967–975. Published online 2006 Feb 1. doi: 10.1242/dev.02270

PMCID:: PMC1363729

Abstract Article PDF–1.1M

Select item 65965889.

Extracellular Signals Induce Glycoprotein M6a Clustering of Lipid Rafts and Associated Signaling Molecules

Atsuko Honda, Yasuyuki Ito, Kazuko Takahashi-Niki, Natsuki Matsushita, Motohiro Nozumi, Hidenori Tabata, Kosei Takeuchi, Michihiro Igarashi

J Neurosci. 2017 Apr 12; 37(15): 4046–4064. doi: 10.1523/JNEUROSCI.3319-16.2017

PMCID:: PMC6596588

Abstract Article PDF–5.7M

Select item 596775710.

Laminin-521 Protein Therapy for Glomerular Basement Membrane and Podocyte Abnormalities in a Model of Pierson Syndrome

Meei-Hua Lin, Joseph B. Miller, Yamato Kikkawa, Hani Y. Suleiman, Karl Tryggvason, Bradley L. Hodges, Jeffrey H. Miner

J Am Soc Nephrol. 2018 May; 29(5): 1426–1436. Published online 2018 Feb 22. doi: 10.1681/ASN.2017060690

PMCID:: PMC5967757

Abstract Article

Select item 580818111.

Laminin-Dependent Interaction between Astrocytes and Microglia: A Role in Retinal Angiogenesis

Saptarshi Biswas, Galina Bachay, Julianne Chu, Dale D. Hunter, William J. Brunken

Am J Pathol. 2017 Sep; 187(9): 2112–2127. doi: 10.1016/j.ajpath.2017.05.016

PMCID:: PMC5808181

Abstract Article

Select item 504265512.

Mesencephalic Astrocyte–Derived Neurotrophic Factor as a Urine Biomarker for Endoplasmic Reticulum Stress–Related Kidney Diseases

Yeawon Kim, Heedoo Lee, Scott R. Manson, Maria Lindahl, Bradley Evans, Jeffrey H. Miner, Fumihiko Urano, Ying Maggie Chen

J Am Soc Nephrol. 2016 Oct; 27(10): 2974–2982. Published online 2016 Mar 3. doi: 10.1681/ASN.2014100986

PMCID:: PMC5042655

Abstract Article

Select item 363197713.

Laminins containing the β2 and γ3 chains regulate astrocyte migration and angiogenesis in the retina

Gopalan Gnanaguru, Galina Bachay, Saptarshi Biswas, Germán Pinzón-Duarte, Dale D. Hunter, William J. Brunken

Development. 2013 May 1; 140(9): 2050–2060. doi: 10.1242/dev.087817

PMCID:: PMC3631977

Abstract Article

Select item 317464214.

Forced expression of laminin β1 in podocytes prevents nephrotic syndrome in mice lacking laminin β2, a model for Pierson syndrome

Jung Hee Suh, George Jarad, Rene G. VanDeVoorde, Jeffrey H. Miner

Proc Natl Acad Sci U S A. 2011 Sep 13; 108(37): 15348–15353. Published online 2011 Aug 29. doi: 10.1073/pnas.1108269108

PMCID:: PMC3174642

Abstract Article PDF–1.1M

Select item 308330715.

A Missense LAMB2 Mutation Causes Congenital Nephrotic Syndrome by Impairing Laminin Secretion

Ying Maggie Chen, Yamato Kikkawa, Jeffrey H. Miner

J Am Soc Nephrol. 2011 May; 22(5): 849–858. doi: 10.1681/ASN.2010060632

PMCID:: PMC3083307

Abstract Article

Select item 293590016.

Laminin deficits induce alterations in the development of dopaminergic neurons in the mouse retina

Viktória Dénes, Paul Witkovsky, Manuel Koch, Dale D. Hunter, Germán Pinzón-Duarte, William J. Brunken

Vis Neurosci. Author manuscript; available in PMC 2010 Sep 8.

Published in final edited form as: Vis Neurosci. 2007 Jul–Aug; 24(4): 549–562. Published online 2007 Aug 22. doi: 10.1017/S0952523807070514

PMCID:: PMC2935900

Abstract Article PDF–3.6M

Select item 130759517.

Expression of mutant Ets protein at the neuromuscular synapse causes alterations in morphology and gene expression

Alban de Kerchove d'Exaerde, Jean Cartaud, Aymeric Ravel-Chapuis, Thierry Seroz, Fabien Pasteau, Lindsay M. Angus, Bernard J. Jasmin, Jean-Pierre Changeux, Laurent Schaeffer

EMBO Rep. 2002 Nov; 3(11): 1075–1081. doi: 10.1093/embo-reports/kvf220