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KIAA1468 gene

Known as: HsT885, FLJ33841, KIAA1468 
 
National Institutes of Health

Related topics

Related topics

1 relation
chromosome 18q

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Novel rearrangements involving the RET gene in papillary thyroid carcinoma.
BACKGROUND In the field of gene fusions driving tumorigenesis in papillary thyroid carcinoma (PTC), rearrangement of the proto… Expand
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2018
2018
The Rab11-binding protein RELCH/KIAA1468 controls intracellular cholesterol distribution
Cholesterol, which is endocytosed to the late endosome (LE)/lysosome, is delivered to other organelles through vesicular and… Expand
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2016
2016
Using an Inbred Horse Breed in a High Density Genome-Wide Scan for Genetic Risk Factors of Insect Bite Hypersensitivity (IBH)
While susceptibility to hypersensitive reactions is a common problem amongst humans and animals alike, the population structure… Expand
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2016
2016
A single-nucleotide polymorphism in transferrin is associated with soluble transferrin receptor levels in Chinese adolescents
Background and Objective: Associations between genetic variants in the hepcidin regulation pathway and iron status have been… Expand
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2013
2013
A single-nucleotide polymorphism in transferrin is associated with soluble transferrin receptor in Chinese adolescents.
BACKGROUND AND OBJECTIVES Associations between genetic variants in the hepcidin regulation pathway and iron status have been… Expand
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Highly Cited
2009
Highly Cited
2009
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
Recent advances in next generation sequencing have made it possible to precisely characterize all somatic coding mutations that… Expand
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2009
2009
More powerful haplotype sharing by accounting for the mode of inheritance.
The concept of haplotype sharing (HS) has received considerable attention recently, and several haplotype association methods… Expand
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Highly Cited
2002
Highly Cited
2002
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22
Chronic recurrent multifocal osteomyelitis (CRMO) is characterised by recurrent inflammatory lesions in the metaphyses of long… Expand
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