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■ Search Result - Abbreviation : LMNA

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Abbreviation: LMNA
Appearance Frequency: 285 time(s)
Long forms: 14

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
lamin A/C
(160 times)
(28 times)
DCM (26 times)
HGPS (15 times)
EDMD (12 times)
2001 Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene.
lamin A/C gene
(103 times)
(20 times)
DCM (16 times)
HGPS (10 times)
EDMD (6 times)
1999 Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
(8 times)
(4 times)
LGMD1B (2 times)
ARCMT (1 time)
BANF1 (1 time)
2002 The nuclear muscular dystrophies.
lamins A and C
(3 times)
(1 time)
AD-EDMD (1 time)
DCM (1 time)
LBR (1 time)
2004 Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Labelled Multilevel Neighbourhood of Atom
(2 times)
(1 time)
AUC (1 time)
IAP (1 time)
SOMs (1 time)
2014 Metabolism site prediction based on xenobiotic structural formulas and PASS prediction algorithm.
(1 time)
(1 time)
LAMC (1 time)
Marf (1 time)
NE (1 time)
2016 Lamin Mutations Accelerate Aging via Defective Export of Mitochondrial mRNAs through Nuclear Envelope Budding.
lamin A is encoded by thelamin A/C
(1 time)
(1 time)
ChIP-seq (1 time)
Dam (1 time)
EDMD (1 time)
2016 Laminopathies disrupt epigenomic developmental programs and cell fate.
Lamin A/C assocated
(1 time)
(1 time)
--- 2020 Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy.
Lamin A/C encoding gene
(1 time)
Genetics, Medical
(1 time)
APS (1 time)
HGPS (1 time)
NGPS (1 time)
2012 An inherited LMNA gene mutation in atypical Progeria syndrome.
10  lamina protein
(1 time)
(1 time)
--- 2006 Genetic basis of lipodystrophies and management of metabolic complications.
11  large database for missense variants in a single gene
(1 time)
Genetic Phenomena
(1 time)
T2D (1 time)
2017 LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes.
12  LMNA gene
(1 time)
(1 time)
PCCD (1 time)
2016 [Mutation screening for the causative gene in a four-generation Chinese pedigree with progressive cardiac conduction defect].
13  low Mach number approximation
(1 time)
Natural Science Disciplines
(1 time)
--- 2002 Multiscale lattice Boltzmann schemes for low Mach number flows.
14  low-methoxyl non-amidated pectin
(1 time)
(1 time)
DON (1 time)
LMA (1 time)
2013 Formulation of a pectin gel that efficiently traps mycotoxin deoxynivalenol and reduces its bioavailability.