Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome (Q41939022)

14 October 2017

Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome (English)

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14 October 2017

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Martin Zenker

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Andreas Dietrich

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Verena Matejas

2

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Martin Bitzan

3

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Seema Hashmi

4

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Cathy Kiraly-Borri

5

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Shuan-Pei Lin

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Eva Mildenberger

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Bernd Hoppe

8

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Lars Palm

9

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Jens-Oliver Steiss

11

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Jeng-Daw Tsai

12

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Udo Vester

13

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Stefanie Weber

14

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Elke Wühl

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Kristina Zepf

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2 July 2008

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1779-1786

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https://scigraph.springernature.com/pub.10.1007/s00467-008-0880-4

14 October 2017

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cites work

Mice deficient in alpha-actinin-4 have severe glomerular disease

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Crossref

https://api.crossref.org/works/10.1007%2FS00467-008-0880-4

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

21 January 2018

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12 December 2020

Distinct functions of alpha3 and alpha(v) integrin receptors in neuronal migration and laminar organization of the cerebral cortex.

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12 December 2020

alpha3beta1 integrin modulates neuronal migration and placement during early stages of cerebral cortical development

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12 December 2020

Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome.

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12 December 2020

Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation

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12 December 2020

Nephrotic syndrome, microcephaly, and developmental delay: three separate syndromes

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12 December 2020

Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs

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12 December 2020

Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome

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12 December 2020

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

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12 December 2020

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome

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12 December 2020

Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?

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12 December 2020

Diffuse mesangial sclerosis: association with unreported congenital anomalies and placental enlargement.

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12 December 2020

Kidney in Galloway-Mowat syndrome: clinical spectrum with description of pathology

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12 December 2020

Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy

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12 December 2020

A milder variant of Pierson syndrome.

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12 December 2020

Mechanism of the process formation; podocytes vs. neurons

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12 December 2020

Getting a foothold in nephrotic syndrome

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12 December 2020

Morphogenetic activity of extracellular matrices on cultured podocytes. Laminin accelerates podocyte process formation in vitro

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12 December 2020

Podocyte proteins in Galloway-Mowat syndrome

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12 December 2020

A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease

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12 December 2020

Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin

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12 December 2020

A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2

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12 December 2020

Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay

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12 December 2020

Roles for laminin in embryogenesis: exencephaly, syndactyly, and placentopathy in mice lacking the laminin alpha5 chain

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12 December 2020

Regulation of adhesive interaction between podocytes and glomerular basement membrane

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12 December 2020

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

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12 December 2020

Alpha 3 beta 1 integrin has a crucial role in kidney and lung organogenesis

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12 December 2020

Prenatal magnetic resonance imaging of Galloway-Mowat syndrome

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12 December 2020

Laminin functions in tissue morphogenesis.

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12 December 2020

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12 December 2020

Galloway-Mowat syndrome: a glomerular basement membrane disorder?

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12 December 2020

Genetic abnormalities and clinical classification of epidermolysis bullosa

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12 December 2020

Congenital microcephaly, hiatus hernia and nephrotic syndrome: an autosomal recessive syndrome

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12 December 2020

Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome

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12 December 2020

10.1007/S00467-008-0880-4

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DOI

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Dimensions Publication ID

14 October 2017

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