|
| |
LAMB2
Gene Information from Publications |
| Publication Link |
Summary of findings |
| 17371932 |
Observational study of genotype prevalence. (HuGE Navigator) |
| 18058136 |
Observational study of genotype prevalence. (HuGE Navigator) |
| 16912710 |
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. |
| 15367484 |
Deficiency in LAMB2 causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. |
| 16146715 |
laminin isoform changes are associated with brain tumor invasion and angiogenesis [review] |
| 16898484 |
Mutations in the LAMB2 gene encoding laminin beta2, a component of the glomerular basement membrane and the neuro-muscular junction are responsible for the characteristic renal and eye abnormalities of Pierson syndrome. |
| 16921188 |
LAMB2 has to be considered as culprit of milder disorders including nephrosis and variable ocular anomalies. |
| 15603881 |
Hepalaminin, an autoantigen from chronic hepatitis C, consists of two domains of laminin beta-2 and a specific domain. |
| 11891225 |
Laminin-10/11 and fibronectin differentially prevent apoptosis induced by serum removal via phosphatidylinositol 3-kinase/Akt- and MEK1/ERK-dependent pathways (Laminin 10; separate entry for Laminin 11). |
Recent Publications on LAMB2: |  |
The first Chinese Pierson syndrome with novel mutations in LAMB2.
Background. Pierson syndrome is typically manifested with congenital... | 29th October, 2009
| 1Department of Pediatrics, Peking University First Hospital, Beijing
| Nephrol Dial Transplant. 2009 Oct 26.
DOI Direct Link |
The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.
The skeletal muscle basement membrane fulfils several crucial functions... | 15th October, 2009
| The Victor Chang Cardiac Research Institute, Darlinghurst, NSW 2010,
| Development. 2009 Oct;136(19):3367-76.
DOI Direct Link |
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome.
BACKGROUND: We describe a severe form of congenital myasthenic syndrome... | 22nd May, 2009
| Department of Neurology, University of California Davis, Davis, CA, 95618,
| J Med Genet. 2009 Mar;46(3):203-8.
DOI Direct Link |
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.
Galloway-Mowat syndrome (GMS) is a rare autosomal recessive disorder... | 19th November, 2008
| Institute of Human Genetics, University of Erlangen-Nuremberg,
| Pediatr Nephrol. 2008 Oct;23(10):1779-86. Epub 2008 Jul 2.
DOI Direct Link |
Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis.
Molecular and genetic studies in the last 2 decades have shed new light on... | 29th October, 2008
| Department of Pathology & Immunology, Washington University School of
| Pediatr Dev Pathol. 2008 Jul-Aug;11(4):154-63.
DOI Direct Link |
→View more research publications. |
LAMB2 results (if any) from reagent suppliers | 
|
Laminin β-2 (H-300) Antibody sc-20777
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Human, LAMB2, 3913, 3p21.31, NM_002292 ...
http://www.scbt.com/datasheet-20777-laminin-beta-2-h-300-ant...
|
 |
L8271 Monoclonal Anti-Laminin antibody produced in mouse clone LAM ...
LAMA1(284217), LAMA2(3908), LAMB1(3912), LAMB2(3913). shipped in, dry ice. storage temp. −20°C. Safety. WGK Germany, 3. References ...
http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=L827...
|
 |
Antibodies to Extracellular Matrix Proteins
LAMA1(284217), LAMA2(3908), LAMB1(3912), LAMB2(3913), pig, human, feline rat, rabbit, snake, goat, guinea pig, mouse, sheep, canine, chicken, frog, carp, ...
http://www.sigmaaldrich.com/etc/controller/controller-page.h...
|
 |
Search Bioportfolio and other Life Science Sites for LAMB2,
or search for LAMB2 on BioPortfolio's antibody search engine.
This page has been viewed 108 times
Recent Search Terms used to find this page: LAMB2 | .
Resources from the NCBI used on this page, NCBI's standard disclaimer applies.
|
