01228cam0 2200289 450 E60020006137320240108095540.020100310d1961 |||||ita|0103 baitaITLiguriaClaudia MerloTorinoUnione Tipografico-Editrice Torinese1961XIV, 540 p.341 ill. : 30 c. geogr. : 1 c. geogr. f.t. : 6 tav. col. f.t.29 cmLe regioni d'ItaliadirRoberto Almagià6Pubblicata sotto gli auspici del Comitato ordinatore della Mostra delle Regioni Italiane : Comitato nazionale per la celebrazione del Primo Centenario dell'Unità d'Italia : 1861-1961001LAEC000283202001 *Le regioni d'Italia / dir. Roberto Almagià6Merlo, ClaudiaA60020006035607010240Almagià, RobertoSOBA00008905070ITUNISOB20240108RICAUNISOBUNISOB910|Coll|23|K7960E600200061373M 102 Monografia moderna SBNM910|Coll|23|K000006Si7960AcquistovittoriniUNISOBUNISOB20100310102315.020240108095540.0SpinosaLiguria314653UNISOB01796nam0 22003611i 450 UON0005024920231205102222.94220020107g19421948 |0itac50 baengARAURDIN||||b |||||ˆA ‰Descriptive catalogue of the Persian, Urdu & Arabic manuscripts in the Punjab University Librarycompiled by S. M. AbdullahLahoreUniversity of Punjab1942-482 v.in 124 cmAltro inv. IND 994IT-UONSI IRAGENC I/002MANOSCRITTI ARABICataloghiUONC000767FIMANOSCRITTI PERSIANICATALOGHIUONC006125FIMANOSCRITTI URDUCATALOGHIUONC010592FIPKLahoreUONL000599IRA GEN C IIRAN - OPERE GENERALI - CATALOGHI - OPERE INTERDISCIPLINARIAABDULLAHSayyid MohammadUONV017945Punjab University LibraryLahoreUONV031752650892University of PunjabUONV253898650ITSOL20240220RICASIBA - SISTEMA BIBLIOTECARIO DI ATENEOUONSIUON00050249SIBA - SISTEMA BIBLIOTECARIO DI ATENEOSI IRA GEN C I 002 SI IND993 7 002 Altro inv. IND 994IRAN - CATALOGHI - MANOSCRITTIMANOSCRITTI PERSIANI - CATALOGHIUONC006255LETTERATURA PERSIANAMANOSCRITTI PERSIANI - CATALOGHIUONC006243LINGUA PERSIANAMANOSCRITTI PERSIANI - CATALOGHIUONC005500MINIATURA - IRANMANOSCRITTI PERSIANI - CATALOGHIUONC006409Descriptive catalogue of the Persian, Urdu & Arabic manuscripts in the Punjab University Library1147641UNIOR04329nam 2201129z- 450 991058594110332120220812(CKB)5600000000483071(oapen)https://directory.doabooks.org/handle/20.500.12854/91136(oapen)doab91136(EXLCZ)99560000000048307120202208d2022 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierCellular and Molecular Mechanisms of Nephropathic CystinosisBaselMDPI - Multidisciplinary Digital Publishing Institute20221 online resource (230 p.)3-0365-4568-9 3-0365-4567-0 Nephropathic cystinosis (MIM # 219800) is a rare autosomal recessive disorder caused by mutations in the lysosomal cystine transporter cystinosin, encoded by the CTNS gene (17p13.2). This devastating condition initially affects kidneys and subsequently many other organs including eyes, thyroid, pancreas, muscles, and brain. While lysosomal cystine storage is a key feature of the disease and the main target of current therapy, recent groundbreaking research has revealed that cystinosin has diverse functions in cells, being involved in vesicle trafficking, energy homeostasis, and cell death mechanisms. These discoveries deepen our insights into the mechanisms of cystinosis and of lysosomal biology in general. In this Special Issue dedicated to the pioneer of cystinosis research Dr. Jerry Schneider, we highlight the state-of-the-art understanding of cellular and molecular mechanisms of various disease features, opening new horizons for innovative treatment strategies for cystinosis and potentially other lysosomal storage diseases.Medicine and NursingbicsscPharmacologybicssc3-dimensional modelsapoptosisarterial spin labellingautophagyazoospermiabiomarkersbonebone-muscle wastingCD34+ hematopoietic stem and progenitor cellscell and animal modelscell modelcentral nervous systemchitotriosidaseclinical courseclinical trialcortical atrophyCTNS-pathogenic variantscysteaminecystinecystine blood levelcystinosisdisulfiramendocytosisendolysosomeepithelial cell differentiationfertilityfibroblast growth factor 23fracturesgalectin-3gene therapygenotypehistopathologyhistoryhollow fiber membranehomeostasishypogonadisminfantile nephropathic cystinosisinflammasomeinterleukinsinvestigational new drug applicationkidneykidney progenitorskidney proximal tubuleleptinlysosomal storage diseaselysosomal storage diseaseslysosomal storage disordermacrophagesmicemitochondrial distressmouse modelnephropathic cystinosisnewborn screeningnewborn screening for cystinosisnovel therapiesosteoclastosteoclastspre-clinical studiesprogrammed cell deathproximal tubular cellssclerostintherapeutic monitoringtreatment strategies for cystinosiszebrafishMedicine and NursingPharmacologyLevtchenko Elena Nedt1318511Levtchenko Elena NothBOOK9910585941103321Cellular and Molecular Mechanisms of Nephropathic Cystinosis3033346UNINA