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FIM-C.1 protein, Xenopus
Known as:
frog integumentary mucin C.1
National Institutes of Health
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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
R. Batista
,
J. Vinagre
,
+31 authors
P. Soares
Front. Genet.
2019
Corpus ID: 209387232
Bladder cancer (BC), the most frequent malignancy of the urinary system, is ranked the sixth most prevalent cancer worldwide. Of…
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2015
2015
Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension
Guillermo Pousada
,
A. Baloira
,
D. Valverde
Orphanet Journal of Rare Diseases
2015
Corpus ID: 18485361
BackgroundPulmonary arterial hypertension (PAH) is a rare and progressive vascular disorder characterized by increased pulmonary…
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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.
V. Brancaleoni
,
F. Granata
,
A. Colancecco
,
D. Tavazzi
,
M. Cappellini
,
E. Di Pierro
Blood cells, molecules & diseases
2012
Corpus ID: 46815283
2012
2012
Improve the Understanding of Uncertainties in Numerical Analysis of Moored Floating Wave Energy Converters
Andrew Vickers
2012
Corpus ID: 106999015
The wave energy industry, still in its infancy compared to similar activities offshore, must look to the oil and gas industry for…
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Review
2009
Review
2009
Modic changes and interleukin 1 gene locus polymorphisms in occupational cohort of middle-aged men
J. Karppinen
,
S. Solovieva
,
K. Luoma
,
R. Raininko
,
P. Leino-Arjas
,
H. Riihimäki
European Spine Journal
2009
Corpus ID: 21906894
According to recent systematic reviews, Modic changes are associated with low-back pain. However, their pathophysiology remains…
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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.
E. Masson
,
C. Le Maréchal
,
+5 authors
C. Férec
Molecular genetics and metabolism
2007
Corpus ID: 23640644
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
D. Baumgart
,
C. Büning
,
+12 authors
A. Dignass
Digestion
2007
Corpus ID: 207679206
Background: Inflammatory bowel disease (IBD) results from an aberrant immune response to the indigenous intestinal flora in…
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2007
2007
Gene dosage analysis identifies large deletions of the FECH gene in 10% of families with erythropoietic protoporphyria.
S. Whatley
,
N. Mason
,
S. A. Holme
,
A. Anstey
,
G. Elder
,
M. Badminton
The Journal of investigative dermatology
2007
Corpus ID: 38725041
Erythropoietic protoporphyria (EPP) is an inherited cutaneous porphyria characterized by partial deficiency of ferrochelatase…
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2007
2007
Statistical analysis of genotype and gene expression data
H. Schwender
2007
Corpus ID: 61296767
A common and important goal in cancer research is the identification of genetic markers such as genes or genetic variations that…
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2005
2005
Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1.
L. Messiaen
,
K. Wimmer
Journal of medical genetics
2005
Corpus ID: 34090602
Mattocks et al 1 have used direct DNA sequencing and comparative sequence analysis to study patients with neurofibromatosis type…
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