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FIM-C.1 protein, Xenopus

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

Related topics

Related topics

1 relation

Broader (1)

Mucins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Validation of a Novel, Sensitive, and Specific Urine-Based Test for Recurrence Surveillance of Patients With Non-Muscle-Invasive Bladder Cancer in a Comprehensive Multicenter Study
Bladder cancer (BC), the most frequent malignancy of the urinary system, is ranked the sixth most prevalent cancer worldwide. Of… Expand
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2015
2015
Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension
BackgroundPulmonary arterial hypertension (PAH) is a rare and progressive vascular disorder characterized by increased pulmonary… Expand
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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… Expand
2012
2012
Improve the Understanding of Uncertainties in Numerical Analysis of Moored Floating Wave Energy Converters
The wave energy industry, still in its infancy compared to similar activities offshore, must look to the oil and gas industry for… Expand
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… Expand
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2007
2007
Co-inheritance of a novel deletion of the entire SPINK1 gene with a CFTR missense mutation (L997F) in a family with chronic pancreatitis.
Quantitative fluorescent multiplex PCR (QFM-PCR) was established in order to make possible the rapid and efficient mutational… Expand
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… Expand
2007
2007
Statistical analysis of genotype and gene expression data
A common and important goal in cancer research is the identification of genetic markers such as genes or genetic variations that… Expand
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2007
2007
Propriétés de transport électronique de nanotubes de carbone: des nanotubes hybrides au nano-SQUID
L'electronique moleculaire et la spintronique moleculaire sont deux domaines emergeant de la nanophysique, prometteurs pour… Expand
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2005
2005
Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1.
Mattocks et al 1 have used direct DNA sequencing and comparative sequence analysis to study patients with neurofibromatosis type… Expand
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