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LAMA2
Gene Information from Publications |
| Publication Link |
Summary of findings |
| 12100448 |
Observational study of gene-disease association. (HuGE Navigator) |
| 16084089 |
DNA analysis can be used to provide accurate prenatal diagnosis of thecongenital muscular dystrophy, and have an essential role in genetic counseling. |
| 11584042 |
case series and review of laminin alpha2(merosin) deficiency phenotypes and abnormalities |
| 16504180 |
suggest that LNalpha1 chain in part ameliorates the development of LNalpha2 chain deficient muscular dystrophy by retaining the binding sites for integrin alpha7Bbeta1D and alpha-dystroglycan, respectively |
| 11938437 |
A number of mutations are identified in association with congenital muscular dystrophies. |
| 12609502 |
However, dy(W)/dy(W) mice, expressing the human laminin alpha2 under the control of the striated muscle-specific portion of the desmin promoter, still developed muscular dystrophy. |
| 16226104 |
A relocalization of LAMA2 was noted in the subepithelial basement membrane in a group of Hirschsprung patients. |
| 12552556 |
In nine congenital muscular dystrophy patients with abnormal white-matter signal at brain MRI and partial deficiency of muscle laminin alpha 2, three novel missense and two splice-site mutations were found. |
| 16216942 |
identified 9 new LAMA 2 mutations |
| 15452315 |
A mild case of autosomal recessive congenital muscular dystrophy is associated with a homozygous out-of-frame deletion in exon 56 of the LAMA2 gene. | →View more information from publications. |
Recent Publications on LAMA2: |  |
Laminin alters fyn regulatory mechanisms and promotes oligodendrocyte development.
Mutations in LAMA2, the gene for the extracellular matrix protein... | 10th October, 2009
| Department of Pharmacology, Stony Brook University, New York 11794, USA.
| J Neurosci. 2009 Sep 23;29(38):11794-806.
DOI Direct Link |
Ku70 regulates Bax-mediated pathogenesis in laminin-{alpha}2-deficient human muscle cells and mouse models of congenital muscular dystrophy.
The severely debilitating disease Congenital Muscular Dystrophy Type 1A... | 21st August, 2009
| Neuromuscular Biology & Disease Group and.
| Hum Mol Genet. 2009 Aug 19.
DOI Direct Link |
LAMA2 stop-codon mutation: merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression.
Merosin-deficient congenital muscular dystrophy (MD) type 1A (MDC1A) is... | 10th March, 2009
| Division of Child Neuropsychiatry, ASL2-Martini Hospital, Turin, Italy.
| Eur J Paediatr Neurol. 2009 Jan;13(1):72-6. Epub 2008 Apr 11.
DOI Direct Link |
Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role.
We undertook in this study the first successful prenatal diagnoses of... | 4th March, 2009
| Laboratoire de Genetique Moleculaire Humaine, Faculte de Medecine de Sfax,
| Genet Test. 2008 Dec;12(4):581-6.
DOI Direct Link |
LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.
Congenital muscular dystrophy type 1A (MDC1A) is caused by mutations in... | 5th February, 2009
| Unidade de Genetica Molecular, Centro de Genetica Medica Dr Jacinto
| Clin Genet. 2008 Dec;74(6):502-12. Epub 2008 Jun 11.
DOI Direct Link |
→View more research publications. |
LAMA2 results (if any) from reagent suppliers | 
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Laminin α-2 (H-130) Antibody sc-20142
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Human, LAMA2, 3908, 6q22.33, NM_000426 ...
http://www.scbt.com/datasheet-20142-laminin-alpha-2-h-130-an...
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Abgent - Cell and Structure Antibodies - Cell_structure
AT2668a, LAMA2 monoclonal antibody (M01), ELISA,IHC-P,WB-Re, H. AT2669a, LAMA5 monoclonal antibody (M01), ELISA,S-ELISA,WB-Re, H ...
http://www.abgent.com/products/category/cell_function/cell_s...
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Antibodies to Extracellular Matrix Proteins
Lama2(16773) human ... LAMA2(3908), mouse, human, ARR, IF (i), pricing. M5293, Monoclonal Anti-Mucin Gastric antibody produced in mouse, 45M1 (monoclonal) ...
http://www.sigmaaldrich.com/etc/controller/controller-page.h...
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Laminin α-2 siRNA (m) sc-43144
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Mouse, Lama2, 16773, 10 A4, Q60675 ...
http://www.scbt.com/datasheet-43144-laminin-alpha-2-sirna-m....
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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...
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Laminin α-2 siRNA (m) sc-43144
Spezies, Gen, Gen ID, Chromosomaler Locus, mRNA (Isoform) Accession #, Protein Accession #, OMIM™ Nummer. Maus, Lama2, 16773, 10 A4, Q60675 ...
http://www.scbt.com/de/datasheet-43144-laminin-alpha-2-sirna...
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Laminin Antibody / Laminin Antibodies
製品名, カタログ番号, アイソタイプ, エピトープ, アプリケーション, 動物種. Laminin α-1 (C-20) 抗体, sc-6016, goat IgG, C-terminus (h), WB, IF, ELISA, human
...
http://www.scbt.com/ja/table-laminin.html...
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