Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35

Renal handling of phosphate and sulfate.

Comprehensive Physiology·2014

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

Clinical genetics·2011

Regulation of phosphate transport in proximal tubules.

Pflugers Archiv : European journal of physiology·2008

Intestinal phosphate absorption in a model of chronic renal failure.

Kidney international·2007

Ifosfamide metabolites CAA, 4-OH-Ifo and Ifo-mustard reduce apical phosphate transport by changing NaPi-IIa in OK cells.

Kidney international·2006

Proximal tubular handling of phosphate: A molecular perspective.

Kidney international·2006

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Genomics·2026

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Genomics·2026

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

Genomics·2026

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Genomics·2026

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

Genomics·2026

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Genomics·2026

WFS1 Deficiency Impairs PIAS4-Associated SUMOylation and Increases Ubiquitin-Mediated Spermatogenesis-Related Protein Degradation Leading to Testicular Male Infertility.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Neurogenetics·2026

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Vavilovskii zhurnal genetiki i selektsii·2026

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

Frontiers in endocrinology·2026

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Vavilovskii zhurnal genetiki i selektsii·2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genome research·2026

Related Experiment Videos

Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35

Related Concept Videos

Renal handling of phosphate and sulfate.

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

Regulation of phosphate transport in proximal tubules.

Intestinal phosphate absorption in a model of chronic renal failure.

Ifosfamide metabolites CAA, 4-OH-Ifo and Ifo-mustard reduce apical phosphate transport by changing NaPi-IIa in OK cells.

Proximal tubular handling of phosphate: A molecular perspective.

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

WFS1 Deficiency Impairs PIAS4-Associated SUMOylation and Increases Ubiquitin-Mediated Spermatogenesis-Related Protein Degradation Leading to Testicular Male Infertility.

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Related Experiment Videos

Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35

Related Concept Videos

Related Articles