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Sjogren-Larsson Syndrome

Known as: ICHTHYOSIS, SPASTIC NEUROLOGIC DISORDER, AND OLIGOPHRENIA, Sjogren Larsson syndrome, Sjögren-Larsson Syndrome 
An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS… 
National Institutes of Health

Related topics

Related topics

18 relations
Autosomal recessive inheritanceCentral nervous system demyelinationCongenital ichthyosisDental Enamel Hypoplasia

Narrower (1)

Sjogren-Larsson-like syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2019
Highly Cited
2019
Strigolactone perception and deactivation by a hydrolase receptor DWARF14
The perception mechanism for the strigolactone (SL) class of plant hormones has been a subject of debate because their receptor… 
Highly Cited
2013
Highly Cited
2013
Strigolactone/MAX2-induced degradation of brassinosteroid transcriptional effector BES1 regulates shoot branching.
Review
2013
Review
2013
Structure and activity of strigolactones: new plant hormones with a rich future.
Strigolactones (SLs) constitute a new class of plant hormones which are active as germination stimulants for seeds of parasitic… 
Review
2011
Review
2011
Perspectives on sesquiterpene lactones in inflammation and cancer.
Sesquiterpene lactones are a large group of secondary plant metabolites mostly known from the Asteraceae family. They exert a… 
Highly Cited
2007
Highly Cited
2007
COMPLEX PREDICATES INVOLVING EVENTS, TIME AND ASPECT: IS THIS WHY SIGN LANGUAGES LOOK SO SIMILAR?
This paper presents a novel perspective on the complex structure of predicate signs, addressing the mapping between semantic… 
Review
2007
Review
2007
Do Student Success Courses Actually Help Community College Students Succeed? CCRC Brief. Number 36.
Many first-time college students arrive on campus unprepared to succeed in college. This is especially the case at community… 
Review
2005
Review
2005
Sjögren‐Larsson syndrome: Diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2)
Sjögren‐Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, and spastic… 
Review
2001
Review
2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome.
Sjögren-Larsson syndrome (SLS) is an autosomal recessively inherited neurocutaneous disorder caused by a deficiency of the… 
Highly Cited
1999
Highly Cited
1999
Inhibition of transcription factor NF-kappaB by sesquiterpene lactones: a proposed molecular mechanism of action.
Highly Cited
1991
Highly Cited
1991
Sjögren-Larsson syndrome. Deficient activity of the fatty aldehyde dehydrogenase component of fatty alcohol:NAD+ oxidoreductase in cultured fibroblasts.
Sjögren-Larsson syndrome (SLS) is an inherited disorder associated with impaired fatty alcohol oxidation due to deficient… 
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