نتائج البحث - "phosphate transport"

1

Evidence of an intestinal phosphate transporter alternative to type IIb sodium-dependent phosphate transporter in rats with chronic kidney disease

المؤلفون: Hiroko Segawa, Yasuhiro Ichida, Ken-ichi Miyamoto, Naoaki Murao, Shuichi Ohtomo, Tessai Yamamoto, Jürgen Floege, Yoshinori Tsuboi, Naoshi Horiba, Yoshiki Kawabe

المصدر: Nephrology Dialysis Transplantation

مصطلحات موضوعية: Male, NaPi-IIb, 0301 basic medicine, medicine.medical_specialty, Brush border, Sodium, 030232 urology & nephrology, chemistry.chemical_element, Sodium-Phosphate Cotransporter Proteins, Type IIb, Phosphates, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Downregulation and upregulation, Internal medicine, PiT, Animals, Phosphate Transport Proteins, Medicine, Rats, Wistar, Renal Insufficiency, Chronic, AcademicSubjects/MED00340, intestine, phosphate, Transplantation, Messenger RNA, Sodium-Phosphate Cotransporter Proteins, Type III, business.industry, Adenine, Transporter, Phosphate, medicine.disease, Rats, Inbred F344, Small intestine, Rats, Intestines, Basic Research, 030104 developmental biology, Endocrinology, medicine.anatomical_structure, chemistry, Nephrology, ORIGINAL ARTICLES, Transcription Factor Pit-1, business, chronic kidney disease, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b7f149b6c1f84caffd37edf5323920bTest
https://doi.org/10.1093/ndt/gfaa156Test

2

Restriction of Dietary Phosphate Ameliorates Skeletal Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia

المؤلفون: Ernst J Reichenberger, I-Ping Chen, András Váradi, Eszter Kozák, Yasuyuki Fujii, Eliane H Dutra

المصدر: J Bone Miner Res

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Mutant, chemistry.chemical_element, 030209 endocrinology & metabolism, Protein degradation, Calcium, Pyrophosphate, Article, Phosphates, Craniofacial Abnormalities, Mice, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Osteoclast, Internal medicine, medicine, Pi, Vitamin D and neurology, Animals, Humans, Phosphate Transport Proteins, Orthopedics and Sports Medicine, Gene Knock-In Techniques, Craniofacial, Bone Diseases, Developmental, Hypertelorism, business.industry, Hyperostosis, Diet, Disease Models, Animal, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, chemistry, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ed0ce9481ac406b6986af625a5f385Test
https://doi.org/10.1002/jbmr.4110Test

3

Genetic locus responsible for diabetic phenotype in the insulin hyposecretion (ihs) mouse

المؤلفون: Nobuya Sasaki, Tadashi Okamura, Yuki Takahashi, Masaki Watanabe, Rieko Yanobu-Takanashi, Kenta Nakano, Koki Hiura, Yukiko Shimizu, Hayato Sasaki

المصدر: PLoS ONE
PLoS ONE, Vol 15, Iss 6, p e0234132 (2020)

مصطلحات موضوعية: 0301 basic medicine, Blood Glucose, Genetic Linkage, Physiology, medicine.medical_treatment, Oral Glucose Suppression Test, Biochemistry, Impaired glucose tolerance, Mice, Synaptotagmins, 0302 clinical medicine, Endocrinology, Insulin Secretion, Medicine and Health Sciences, Phosphate Transport Proteins, Insulin, Glucose Tolerance, Multidisciplinary, Animal Models, Blood Sugar, Body Fluids, Phenotype, Blood, Experimental Organism Systems, Medicine, Transcriptional Elongation Factors, Anatomy, Research Article, medicine.medical_specialty, Science, Quantitative Trait Loci, Congenic, Blood sugar, Locus (genetics), Mouse Models, Quantitative trait locus, Biology, Research and Analysis Methods, 03 medical and health sciences, Model Organisms, Diabetes mellitus, Internal medicine, medicine, Genetics, Animals, Diabetic Endocrinology, Pharmacology, Endocrine Physiology, Membrane Proteins, Biology and Life Sciences, Glucose Tolerance Test, medicine.disease, Hormones, Pharmacologic-Based Diagnostics, Mice, Inbred C57BL, Disease Models, Animal, 030104 developmental biology, Metabolism, Diabetes Mellitus, Type 2, Genetic Loci, Animal Studies, Insulitis, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d22d7ab96e0d1eceb1c027d5bd61f291Test
https://pubmed.ncbi.nlm.nih.gov/32502168Test

4

Mechanisms and Regulation of Intestinal Phosphate Absorption

المؤلفون: Nati Hernando, Carsten A. Wagner

المساهمون: University of Zurich, Hernando, Nati

المصدر: Comprehensive Physiology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7684897d3e50a9215b5fd23d03b84e3Test
https://doi.org/10.1002/cphy.c170024Test

5

EOS789, a novel pan-phosphate transporter inhibitor, is effective for the treatment of chronic kidney disease-mineral bone disorder

المؤلفون: Shunsuke Nagao, Hitoshi Hagita, Shuichi Ohtomo, Yasuhiro Ichida, Manami Iida, Naoshi Horiba, Yoshinori Tsuboi, Kazuharu Ozawa, Tadakatsu Takahashi, Hisashi Ikegami

المصدر: Kidney international. 98(2)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b978064d3b55effc504de77f9d6c2cc4Test
https://pubmed.ncbi.nlm.nih.gov/32624180Test

6

PiT1 : du transport de phosphate à la signalisation insulinique

المؤلفون: Anne Forand

المصدر: médecine/sciences. 33:480-483

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e4efb55972d7203227a21e270f27fef0Test
https://doi.org/10.1051/medsci/20173305007Test

7

The role of the progressive ankylosis protein (ANK) in adipogenic/osteogenic fate decision of precursor cells

المؤلفون: Thorsten Kirsch, Takeshi Minashima, Martin Quirno, You Jin Lee

المصدر: Bone. 98:38-46

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Histology, Stromal cell, Physiology, Endocrinology, Diabetes and Metabolism, Bone healing, Real-Time Polymerase Chain Reaction, Osteocytes, Article, Mice, 03 medical and health sciences, 0302 clinical medicine, Bone Marrow, Osteogenesis, Internal medicine, Precursor cell, Adipocytes, medicine, Animals, Phosphate Transport Proteins, Wnt Signaling Pathway, Adipogenesis, Chemistry, Mesenchymal stem cell, Wnt signaling pathway, Cell Differentiation, Mesenchymal Stem Cells, Osteoblast, X-Ray Microtomography, Mice, Mutant Strains, Cell biology, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, 030220 oncology & carcinogenesis, Female, Bone marrow

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a8cfd47888f3db4487043c4a8f1603Test
https://doi.org/10.1016/j.bone.2017.03.003Test

8

Regulation of phosphate transport and AMPK signal pathway by lower dietary phosphorus of broilers

المؤلفون: Junzhen Zhang, Wenxia Tian, Jianhui Li, Yu Yang, Zhiqiang Miao, Yan Feng

المصدر: Oncotarget

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab5562dc8ebe516bac79021777b14adTest
https://pubmed.ncbi.nlm.nih.gov/29296204Test

9

Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia

المؤلفون: Klaus Zerres, Stanley F. Nelson, Catriona McLean, Michael Yourshaw, Joanna C. Jen, Sabine Rudnik-Schöneborn, Andrew J. Kornberg, Jijun Wan, Erik Andersen, Kate Pope, Monique M. Ryan, Carla M. Koehler, Janos Steffen, Jörg Joseph, Katherine B. Howell, Hafsa Mamsa, Paul J. Lockhart

المصدر: Brain : a journal of neurology, vol 139, iss 11

مصطلحات موضوعية: Male, Models, Molecular, 0301 basic medicine, Pathology, Embryo, Nonmammalian, Neurodegenerative, Mitochondrion, Medical and Health Sciences, Mitochondrial Dynamics, Animals, Genetically Modified, Cohort Studies, Neurodevelopmental disorder, Models, Mutant protein, 2.1 Biological and endogenous factors, Phosphate Transport Proteins, Missense mutation, Aetiology, Amino Acids, Cells, Cultured, Zebrafish, Cell Line, Transformed, Pediatric, Cultured, Nonmammalian, SLC25A46, Brain, Single Nucleotide, Magnetic Resonance Imaging, Mitochondria, Cell biology, mitochondrial fusion, Embryo, Neurological, optic atrophy spectrum disorder, Female, Mitochondrial fission, medicine.medical_specialty, Cells, Pontocerebellar hypoplasia, Genetically Modified, Biology, Polymorphism, Single Nucleotide, Cell Line, Mitochondrial Proteins, 03 medical and health sciences, Rare Diseases, Atrophy, Cerebellar Diseases, Genetics, medicine, Animals, Humans, Genetic Predisposition to Disease, Polymorphism, Neurology & Neurosurgery, pontocerebellar hypoplasia, Psychology and Cognitive Sciences, Neurosciences, Molecular, Infant, Original Articles, medicine.disease, Brain Disorders, Orphan Drug, 030104 developmental biology, Transformed, Mutation, Congenital Structural Anomalies, Neurology (clinical)

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b44f317e0a7b5646a7f26b75cc2e31Test
https://doi.org/10.1093/brain/aww212Test

10

Dent disease: A window into calcium and phosphate transport

المؤلفون: Lisa Gianesello, Franca Anglani, Lada Beara-Lasic, John C. Lieske

المصدر: Journal of Cellular and Molecular Medicine

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b91372c4ffc9e5c35a60ff113fabe0a5Test
http://hdl.handle.net/11577/3313690Test

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