FAQ

LAMA3 gene

Known as: kalinin-165kDa, nicein-150kDa, LAMA3 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2016
01219922016

Related topics

Related topics

4 relations
LAMA1 geneLAMA4 genelaminin alpha 3laminin-5

Related mentions per year

Related mentions per year

1989-2018
19801990200020102020
LAMA3 gene
LAMA4 gene
laminin-5
LAMA1 gene
laminin alpha 3

Papers overview

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2017
2017
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutation.
 
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2013
2013
LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta.
Amelogenesis imperfecta (AI) can be either isolated or part of a larger syndrome. Junctional epidermolysis bullosa (JEB) is a… (More)
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2013
2013
Detection of novel LAMA3 mutation in Herlitz junctional epidermolysis bullosa in a Jordanian family.
The Herlitz junctional epidermolysis bullosa (H-JEB) subtype usually presents as a severe lethal inherited variant of… (More)
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2012
2012
Enamel defects in carriers of a novel LAMA3 mutation underlying epidermolysis bullosa.
Fig. S1. (a, b) Agarose gel analysis and (c, d) direct sequencing of mRNA amplified by nested PCRs in the proband and her mother… (More)
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2011
2011
Efficiency of translation termination in humans is highly dependent upon nucleotides in the neighbourhood of a (premature) termination codon.
BACKGROUND Spontaneous read-through of a premature termination codon (PTC) has so far not been observed in patients carrying… (More)
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2010
2010
Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals.
OBJECTIVE The purpose of the present study was to identify genetic variants that confer susceptibility to myocardial infarction… (More)
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2009
2009
Partial deletion of the LAMA3 gene is responsible for hereditary junctional epidermolysis bullosa in the American Saddlebred Horse.
Laminin 5 is a heterotrimeric basement membrane protein integral to the structure and function of the dermal-epidermal junction… (More)
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2008
2008
Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa.
Herlitz junctional epidermolysis bullosa (HJEB) is a rare genodermatosis characterized by blister formation with tissue… (More)
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2007
2007
Novel human pathological mutations. Gene symbol: LAMA3. Disease: junctional epidermolysis bullosa.
 
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1995
1995
Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa.
Laminin 5 and laminin 6 are basement membrane proteins synthesized by the basal cells of stratifying squamous epithelia. Altered… (More)
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