The C‐type lectin‐like domain superfamily
AN Zelensky, JE Gready - The FEBS journal, 2005 - Wiley Online Library
The superfamily of proteins containing C‐type lectin‐like domains (CTLDs) is a large group
of extracellular Metazoan proteins with diverse functions. The CTLD structure has a …
of extracellular Metazoan proteins with diverse functions. The CTLD structure has a …
The TRP superfamily of cation channels
C Montell - Science's STKE, 2005 - science.org
The transient receptor potential (TRP) protein superfamily consists of a diverse group of
cation channels that bear structural similarities to Drosophila TRP. TRP channels play …
cation channels that bear structural similarities to Drosophila TRP. TRP channels play …
Calcium channels in the development, maturation, and function of spermatozoa
A Darszon, T Nishigaki, C Beltran… - Physiological …, 2011 - journals.physiology.org
A proper dialogue between spermatozoa and the egg is essential for conception of a new
individual in sexually reproducing animals. Ca2+ is crucial in orchestrating this unique event …
individual in sexually reproducing animals. Ca2+ is crucial in orchestrating this unique event …
Polycystin-2 is an intracellular calcium release channel
P Koulen, Y Cai, L Geng, Y Maeda, S Nishimura… - Nature cell …, 2002 - nature.com
Polycystin-2, the product of the gene mutated in type 2 autosomal dominant polycystic
kidney disease (ADPKD), is the prototypical member of a subfamily of the transient receptor …
kidney disease (ADPKD), is the prototypical member of a subfamily of the transient receptor …
PKD1 interacts with PKD2 through a probable coiled-coil domain
Autosomal dominant polycystic kidney disease (ADPKD) describes a group of at least three
genetically distinct disorders with almost identical clinical features1–6 that collectively affects …
genetically distinct disorders with almost identical clinical features1–6 that collectively affects …
Genetics and pathogenesis of polycystic kidney disease
P Igarashi, S Somlo - Journal of the American Society of …, 2002 - journals.lww.com
Polycystic kidney disease (PKD), a common genetic cause of chronic renal failure in
children and adults, is characterized by the accumulation of fluid-filled cysts in the kidney …
children and adults, is characterized by the accumulation of fluid-filled cysts in the kidney …
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease
S Rossetti, MB Consugar, AB Chapman… - Journal of the …, 2007 - journals.lww.com
Mutation-based molecular diagnostics of autosomal dominant polycystic kidney disease
(ADPKD) is complicated by genetic and allelic heterogeneity, large multi-exon genes …
(ADPKD) is complicated by genetic and allelic heterogeneity, large multi-exon genes …
[HTML][HTML] Somatic inactivation of Pkd2 results in polycystic kidney disease
G Wu, V D'Agati, Y Cai, G Markowitz, JH Park… - Cell, 1998 - cell.com
Germline mutations in PKD2 cause autosomal dominant polycystic kidney disease. We have
introduced a mutant exon 1 in tandem with the wild-type exon 1 at the mouse Pkd2 locus …
introduced a mutant exon 1 in tandem with the wild-type exon 1 at the mouse Pkd2 locus …
Structure, biology, evolution, and medical importance of sulfated fucans and galactans
VH Pomin, PAS Mourão - Glycobiology, 2008 - academic.oup.com
Sulfated fucans and galactans are strongly anionic polysaccharides found in marine
organisms. Their structures vary among species, but their major features are conserved …
organisms. Their structures vary among species, but their major features are conserved …
Animal lectins
HJ Gabius - European journal of biochemistry, 1997 - Wiley Online Library
Protein and lipid glycosylation is no longer considered as a topic whose appeal is restricted
to a limited number of analytical experts perseveringly pursuing the comprehensive …
to a limited number of analytical experts perseveringly pursuing the comprehensive …