Reno-endocrinal disorders: A basic understanding of the molecular genetics

scientific article published on March 2012

Reno-endocrinal disorders: A basic understanding of the molecular genetics is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.4103/2230-8210.93731
P932PMC publication ID3313731
P698PubMed publication ID22470850
P5875ResearchGate publication ID223983438

P2093author name stringSukhminder Jit Singh Bajwa
Ishwardip Singh Kwatra
P2860cites workMEPE, a new gene expressed in bone marrow and tumors causing osteomalaciaQ24290092
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23Q24290481
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SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasisQ24299058
Isolation and characterization of genomic and cDNA clones of human erythropoietinQ24299960
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Role of sugar chains in the in vitro biological activity of human erythropoietin produced in recombinant Chinese hamster ovary cellsQ41727703
Core erythropoietin receptor signals for late erythroblast developmentQ41996778
Proteasomes regulate the duration of erythropoietin receptor activation by controlling down-regulation of cell surface receptorsQ42489065
In vitro production of erythropoietin by mouse fetal liverQ43603059
Site of 1,25(OH)2 vitamin D3 synthesis in the kidneyQ43812165
Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolismQ44020458
Microheterogeneity of erythropoietin carbohydrate structureQ46150335
Nephrogenic diabetes insipidus: update of genetic and clinical aspectsQ47991177
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.Q52026277
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.Q54943458
Identification of the renal erythropoietin-producing cells using transgenic miceQ57378026
Physicochemical and biological comparison of recombinant human erythropoietin with human urinary erythropoietinQ68788619
Carbohydrate structure of erythropoietin expressed in Chinese hamster ovary cells by a human erythropoietin cDNAQ69222372
Co-localization of erythropoietin mRNA and ecto-5'-nucleotidase immunoreactivity in peritubular cells of rat renal cortex indicates that fibroblasts produce erythropoietinQ70551126
Role of antennary structure of N-linked sugar chains in renal handling of recombinant human erythropoietinQ71570778
Hypocalcemia, morbidity, and mortality in end-stage renal diseaseQ71715176
Control of renal function by intrarenal angiotensin IIQ71726250
Erythropoietin receptors: their role beyond erythropoiesisQ81666653
Suppression by 1,25(OH)2D3 of transcription of the pre-proparathyroid hormone geneQ93557533
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP ConsortiumQ24308202
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.Q24540520
Cloning and expression of the human erythropoietin geneQ24608978
Cloning and expression of full-length cDNA encoding human vitamin D receptorQ24650952
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosisQ28260847
Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidusQ28280046
Erythropoietin retards DNA breakdown and prevents programmed death in erythroid progenitor cellsQ28282130
Concerted action of associated proteins in the regulation of TRPV5 and TRPV6Q28283921
Erythropoietin induces tyrosine phosphorylation of Jak2, STAT5A, and STAT5B in primary cultured human erythroid precursors.Q30176130
Newly recognized components of the renin-angiotensin system: potential roles in cardiovascular and renal regulationQ30310896
Site-specific glycosylation of human recombinant erythropoietin: analysis of glycopeptides or peptides at each glycosylation site by fast atom bombardment mass spectrometryQ30404030
Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongationQ33938586
Sensing, signaling and sorting events in kidney epithelial cell physiologyQ33961141
Relationship between sugar chain structure and biological activity of recombinant human erythropoietin produced in Chinese hamster ovary cellsQ34311306
Molecular biology of hereditary diabetes insipidus.Q34442011
Regulation of intrarenal angiotensin II in hypertensionQ34554367
Proximal tubular handling of phosphate: A molecular perspectiveQ34563763
Tolvaptan, a selective oral vasopressin V2-receptor antagonist, for hyponatremiaQ34581679
TRPV5, the gateway to Ca2+ homeostasisQ34600636
Erythropoietin after a century of research: younger than everQ34606348
Purification of human erythropoietinQ34777478
The enigma of the metabolic fate of circulating erythropoietin (Epo) in view of the pharmacokinetics of the recombinant drugs rhEpo and NESP.Q35013346
Intrarenal angiotensin II and hypertensionQ35087015
Expression cloning of the murine erythropoietin receptorQ35416452
Turning cells red: signal transduction mediated by erythropoietinQ36064203
Disorders of body water homeostasis in critical illnessQ36663968
New aspect of renal phosphate reabsorption: the type IIc sodium-dependent phosphate transporter.Q36905432
Physiology and pathophysiology of the vasopressin-regulated renal water reabsorptionQ37145917
Aquaporin-2 in the "-omics" eraQ37200830
Aquaporins in kidney pathophysiologyQ37681294
Human proreninQ37687876
Specific binding of 1alpha,25-dihydroxycholecalciferol to nuclear components of chick intestineQ39918477
Vitamin D: recent advancesQ40137018
Fibroblast growth factor 7: an inhibitor of phosphate transport derived from oncogenic osteomalacia-causing tumorsQ40488393
Molecular biology of the renin-angiotensin systemQ40854596
P433issue2
P921main subjectmolecular geneticsQ210506
P304page(s)158-163
P577publication date2012-03-01
P1433published inIndian Journal of Endocrinology and MetabolismQ15816442
P1476titleReno-endocrinal disorders: A basic understanding of the molecular genetics
P478volume16

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cites work (P2860)
Q38115310Anesthetic management of primary hyperparathyroidism: A role rarely noticed and appreciated so far.
Q38255805Endocrine anesthesia: A rapidly evolving anesthesia specialty
Q36426215Peri-operative renal protection: The strategies revisited
Q37239003Pharmaco-genomics and anaesthesia: Mysteries, correlations and facts
Q34196827Predictors of acute kidney injury in geriatric patients undergoing total knee replacement surgery

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