PubMed for id: 16779

Year	Number of Results
1984	1
1985	1
1987	2
1988	1
1990	1
1991	1
1993	1
1994	5
1995	3
1996	6
1997	3
1998	2
1999	4
2000	3
2001	4
2002	6
2003	6
2004	3
2005	4
2006	6
2007	8
2008	6
2009	2
2010	3
2011	8
2012	5
2013	9
2014	4
2015	3
2016	4
2017	9
2018	5
2019	2
2020	2
2021	1
2022	1
2024	0

1

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

Funk SD, Bayer RH, McKee KK, Okada K, Nishimune H, Yurchenco PD, Miner JH. Funk SD, et al. Kidney Int. 2020 Jul;98(1):133-146. doi: 10.1016/j.kint.2020.01.033. Epub 2020 Feb 20. Kidney Int. 2020. PMID: 32456966 Free PMC article.

2

CNS synapses are stabilized trans-synaptically by laminins and laminin-interacting proteins.

Hunter DD, Manglapus MK, Bachay G, Claudepierre T, Dolan MW, Gesuelli KA, Brunken WJ. Hunter DD, et al. J Comp Neurol. 2019 Jan 1;527(1):67-86. doi: 10.1002/cne.24338. Epub 2017 Oct 27. J Comp Neurol. 2019. PMID: 29023785

3

Albumin-associated free fatty acids induce macropinocytosis in podocytes.

Chung JJ, Huber TB, Gödel M, Jarad G, Hartleben B, Kwoh C, Keil A, Karpitskiy A, Hu J, Huh CJ, Cella M, Gross RW, Miner JH, Shaw AS. Chung JJ, et al. J Clin Invest. 2015 Jun;125(6):2307-16. doi: 10.1172/JCI79641. Epub 2015 Apr 27. J Clin Invest. 2015. PMID: 25915582 Free PMC article.

4

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

Chand KK, Lee KM, Schenning MP, Lavidis NA, Noakes PG. Chand KK, et al. J Physiol. 2015 Jan 1;593(1):245-65. doi: 10.1113/jphysiol.2014.284133. Epub 2014 Dec 1. J Physiol. 2015. PMID: 25556799 Free PMC article.

5

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

Bull KR, Mason T, Rimmer AJ, Crockford TL, Silver KL, Bouriez-Jones T, Hough TA, Chaudhry S, Roberts IS, Goodnow CC, Cornall RJ. Bull KR, et al. J Pathol. 2014 May;233(1):18-26. doi: 10.1002/path.4308. Epub 2014 Feb 6. J Pathol. 2014. PMID: 24293254 Free PMC article.

6

Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes.

Chen YM, Zhou Y, Go G, Marmerstein JT, Kikkawa Y, Miner JH. Chen YM, et al. J Am Soc Nephrol. 2013 Jul;24(8):1223-33. doi: 10.1681/ASN.2012121149. Epub 2013 May 30. J Am Soc Nephrol. 2013. PMID: 23723427 Free PMC article.

7

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

Miner JH, Go G, Cunningham J, Patton BL, Jarad G. Miner JH, et al. Development. 2006 Mar;133(5):967-75. doi: 10.1242/dev.02270. Epub 2006 Feb 1. Development. 2006. PMID: 16452099 Free PMC article.

8

Functional analysis of neurotransmission at beta2-laminin deficient terminals.

Knight D, Tolley LK, Kim DK, Lavidis NA, Noakes PG. Knight D, et al. J Physiol. 2003 Feb 1;546(Pt 3):789-800. doi: 10.1113/jphysiol.2002.030924. J Physiol. 2003. PMID: 12563004 Free PMC article.

9

Domain IV of mouse laminin beta1 and beta2 chains.

Sasaki T, Mann K, Miner JH, Miosge N, Timpl R. Sasaki T, et al. Eur J Biochem. 2002 Jan;269(2):431-42. doi: 10.1046/j.0014-2956.2001.02663.x. Eur J Biochem. 2002. PMID: 11856301 Free article.

10

Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS.

Libby RT, Lavallee CR, Balkema GW, Brunken WJ, Hunter DD. Libby RT, et al. J Neurosci. 1999 Nov 1;19(21):9399-411. doi: 10.1523/JNEUROSCI.19-21-09399.1999. J Neurosci. 1999. PMID: 10531444 Free PMC article.

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