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FIM-C.1 protein, Xenopus

Known as: frog integumentary mucin C.1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2007-2017
01220072017

Related topics

Related topics

1 relation

Broader (1)

Mucins

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
FIM-C.1 protein, Xenopus
Mucins

Papers overview

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2017
2017
Novel Genetic Variants in Carboxylesterase 1 Predict Severe Early-Onset Capecitabine-Related Toxicity.
An important concern with the anticancer drug capecitabine (Cp), an oral prodrug of 5-fluorouracil, are dose-limiting adverse… (More)
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2015
2015
Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension
BACKGROUND Pulmonary arterial hypertension (PAH) is a rare and progressive vascular disorder characterized by increased pulmonary… (More)
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2012
2012
Seven novel genetic mutations within the 5'UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria.
Acute intermittent porphyria (AIP) is an autosomal dominant disorder caused by molecular abnormalities in the HMBS gene. This… (More)
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2009
2009
HTR2C gene polymorphisms and the metabolic syndrome in patients with schizophrenia: a replication study.
In a previous study, we found an association between 5-hydroxytryptamine (serotonin) receptor 2C (HTR2C) polymorphisms and the… (More)
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2007
2007
The c.1-260C>T promoter variant of CD14 but not the c.896A>G (p.D299G) variant of toll-like receptor 4 (TLR4) genes is associated with inflammatory bowel disease.
BACKGROUND Inflammatory bowel disease (IBD) results from an aberrant immune response to the indigenous intestinal flora in… (More)
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2007
2007
Gene dosage analysis identifies large deletions of the FECH gene in 10% of families with erythropoietic protoporphyria.
Erythropoietic protoporphyria (EPP) is an inherited cutaneous porphyria characterized by partial deficiency of ferrochelatase… (More)
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