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■ Search Result - Abbreviation : LAMA2

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Abbreviation: LAMA2
Appearance Frequency: 55 time(s)
Long forms: 9

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
laminin alpha2
(21 times)
Science
(3 times)
MDC1A (5 times)
CMD (4 times)
caf (2 times)
2001 Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping.
laminin alpha2 chain gene
(11 times)
Genetics, Medical
(4 times)
CMD (3 times)
CMDs (1 time)
LamA1 (1 time)
1995 Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
laminin alpha2 gene
(9 times)
Genetics, Medical
(2 times)
CMD (5 times)
MDC1A (4 times)
MRI (2 times)
1997 Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis.
laminin subunit alpha 2
(6 times)
Endocrine System Diseases
(2 times)
CMD (1 time)
CT (1 time)
DWI (1 time)
2016 Proteomic-based research strategy identified laminin subunit alpha 2 as a potential urinary-specific biomarker for the medullary sponge kidney disease.
laminin-alpha2 chain
(3 times)
Biology
(1 time)
AChE (1 time)
BuChE (1 time)
CMD (1 time)
1996 Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation.
laminina2-chain gene
(2 times)
Genetics, Medical
(1 time)
CMD (1 time)
2000 Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online.
laminin alpha 2 locus
(1 time)
Neurology
(1 time)
CMD (1 time)
MRI (1 time)
1997 Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency.
laminin alpha 2-chain gene mutations
(1 time)
Biology
(1 time)
--- 1995 Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
Laminin alpha-2 subunit
(1 time)
Stem Cells
(1 time)
hESC (1 time)
NPTN (1 time)
2015 Dynamic Proteomic Analysis of Pancreatic Mesenchyme Reveals Novel Factors That Enhance Human Embryonic Stem Cell to Pancreatic Cell Differentiation.