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La ricerca find articoli where soggetti phrase all words 'PEX GENE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 44 riferimenti
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    1. Nelson, AE; Hogan, JJ; Holm, IA; Robinson, BG; Mason, RS
      Phosphate wasting in oncogenic osteomalacia: PHEX is normal and the tumor-derived factor has unique properties

      BONE
    2. Sabbagh, Y; Boileau, G; DesGroseillers, L; Tenenhouse, HS
      Disease-causing missense mutations in the PHEX gene interfere with membrane targeting of the recombinant protein

      HUMAN MOLECULAR GENETICS
    3. Johnson, MA; Snyder, WB; Cereghino, JL; Veenhuis, M; Subramani, S; Cregg, JM
      Pichia pastoris Pex14p, a phosphorylated peroxisomal membrane protein, is part of a PTS-receptor docking complex and interacts with many peroxins

      YEAST
    4. Beck, L; Silve, C
      Molecular aspects of phosphate homeostasis in mammals

      NEPHROLOGIE
    5. Kaplan, CP; Thomas, JE; Charlton, WL; Baker, A
      Identification and characterisation of PEX6 orthologues from plants

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
    6. Levi, M
      Post-transplant hypophosphatemia

      KIDNEY INTERNATIONAL
    7. Jonsson, KB; Mannstadt, M; Miyauchi, A; Yang, IM; Stein, G; Ljunggren, O; Juppner, H
      Extracts from tumors causing oncogenic osteomalacia inhibit phosphate uptake in opossum kidney cells

      JOURNAL OF ENDOCRINOLOGY
    8. Christie, PT; Harding, B; Nesbit, MA; Whyte, MP; Thakker, RV
      X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    9. Holm, IA; Nelson, AE; Robinson, BG; Mason, RS; Marsh, DJ; Cowell, CT; Carpenter, TO
      Mutational analysis and genotype-phenotype correlation of the PHEX gene inX-linked hypophosphatemic rickets

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    10. Miao, DS; Bai, XY; Panda, D; McKee, MD; Karaplis, AC; Goltzman, D
      Osteomalacia in Hyp mice is associated with abnormal Phex expression and with altered bone matrix protein expression and deposition

      ENDOCRINOLOGY
    11. Meyer, MH; Meyer, RA
      MRNA expression of Phex in mice and rats - The effect of low phosphate diet

      ENDOCRINE
    12. Sabbagh, Y; Jones, AO; Tenenhouse, HS
      PHEXdb, a locus-specific database for mutations causing X-linked hypophosphatemia

      HUMAN MUTATION
    13. DiMeglio, LA; White, KE; Econs, MJ
      Disorders of phosphate metabolism

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    14. Rowe, PSN; de Zoysa, PA; Dong, R; Wang, HR; White, KE; Econs, MJ; Oudet, CL
      MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia

      GENOMICS
    15. Ruchon, AF; Tenenhouse, HS; Marcinkiewicz, M; Siegfried, G; Aubin, JE; Desgroseillers, L; Crine, P; Boileau, G
      Developmental expression and tissue distribution of Phex protein: Effect of the Hyp mutation and relationship to bone markers

      JOURNAL OF BONE AND MINERAL RESEARCH
    16. Miyamura, T; Tanaka, H; Inoue, M; Ichinose, Y; Seino, Y
      The effects of bone marrow transplantation on X-linked hypophosphatemic mice

      JOURNAL OF BONE AND MINERAL RESEARCH
    17. Sundaram, M; McCarthy, EF
      Oncogenic osteomalacia

      SKELETAL RADIOLOGY
    18. Valdenaire, O; Schweizer, A
      Endothelin-converting enzyme-like I (ECELI; 'XCE'): a putative metallopeptidstse crucially involved in the nervous control of respiration

      BIOCHEMICAL SOCIETY TRANSACTIONS
    19. Nilsson, J; Gritli-Linde, A; Heby, O
      Skin fibroblasts from spermine synthase-deficient hemizygous gyro male (Gy/Y) mice overproduce spermidine and exhibit increased resistance to oxidative stress but decreased resistance to UV irradiation

      BIOCHEMICAL JOURNAL
    20. Mackintosh, CA; Pegg, AE
      Effect of spermine synthase deficiency on polyamine biosynthesis and content in mice and embryonic fibroblasts, and the sensitivity of fibroblasts to1,3-bis-(2-chloroethyl)-N-nitrosourea

      BIOCHEMICAL JOURNAL
    21. Valdenaire, O; Rohrbacher, E; Langeveld, A; Schweizer, A; Meijers, C
      Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respiration

      BIOCHEMICAL JOURNAL
    22. Hines, ER; Collins, JF; Ghishan, FK
      Molecular cloning of the murine PHEX gene promoter

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    23. Drezner, MK
      PHEX gene and hypophosphatemia

      KIDNEY INTERNATIONAL
    24. Sato, K; Tajima, T; Nakae, J; Adachi, M; Asakura, Y; Tachibana, K; Suwa, S; Katsumata, N; Tanaka, T; Hayashi, Y; Abe, S; Murashita, M; Okuhara, K; Shinohara, N; Fujieda, K
      Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets

      PEDIATRIC RESEARCH
    25. Rowe, PSN
      The molecular background to hypophosphataemic rickets

      ARCHIVES OF DISEASE IN CHILDHOOD
    26. Econs, MJ
      New insights into the pathogenesis of inherited phosphate wasting disorders

      BONE
    27. Filisetti, D; Ostermann, G; von Bredow, M; Strom, T; Filler, G; Ehrich, J; Pannetier, S; Garnier, JM; Rowe, P; Francis, F; Julienne, A; Hanauer, A; Econs, MJ; Oudet, C
      Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

      EUROPEAN JOURNAL OF HUMAN GENETICS
    28. Wang, LQ; Du, LS; Ecarot, B
      Evidence for Phex haploinsufficiency in murine X-linked hypophosphatemia

      MAMMALIAN GENOME
    29. Tenenhouse, HS
      X-linked hypophosphataemia: a homologous disorder in humans and mice

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    30. Blydt-Hansen, TD; Tenenhouse, HS; Goodyer, P
      PHEX expression in parathyroid gland and parathyroid hormone dysregulationin X-linked hypophosphatemia

      PEDIATRIC NEPHROLOGY
    31. Nesbitt, T; Fujiwara, I; Thomas, R; Xiao, ZS; Quarles, LD; Drezner, MK
      Coordinated maturational regulation of PHEX and renal phosphate transport inhibitory activity: Evidence for the pathophysiological role of PHEX in X-linked hypophosphatemia

      JOURNAL OF BONE AND MINERAL RESEARCH
    32. Kiel, JAKW; Hilbrands, RE; Van der Klei, IJ; Rasmussen, SW; Salomons, FA; Van der Heide, M; Faber, KN; Cregg, JM; Veenhuis, M
      Hansenula polymorpha Pex1p and Pex6p are peroxisome-associated AAA proteins that functionally and physically interact

      YEAST
    33. Patzer, L; van't Hoff, W; Shah, V; Hallson, P; Kasidas, GP; Samuell, C; de Bruyn, R; Barratt, TM; Dillon, MJ
      Urinary supersaturation of calcium oxalate and phosphate in patients with X-linked hypophosphatemic rickets and in healthy schoolchildren

      JOURNAL OF PEDIATRICS
    34. Shimozawa, N; Imamura, A; Zhang, ZY; Suzuki, Y; Orii, T; Tsukamoto, T; Osumi, T; Fujiki, Y; Wanders, RJA; Besley, G; Kondo, N
      Defective PEX gene products correlate with the protein import, biochemicalabnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

      JOURNAL OF MEDICAL GENETICS
    35. Ecarot, B; Desbarats, M
      1,25-(OH)(2)D-3 down-regulates expression of Phex, a marker of the mature osteoblast

      ENDOCRINOLOGY
    36. KAGITANI K; YAMAMOTO T; MIKI K; MATSUMOTO S; SHIMA M; TAJIRI H; HARADA T; OKADA S
      HYPOPHOSPHATEMIC RICKETS ACCOMPANYING CONGENITAL MICROVILLOUS ATROPHY

      Journal of bone and mineral research
    37. TENENHOUSE HS; ROY S; MARTEL J; GAUTHIER C
      DIFFERENTIAL EXPRESSION, ABUNDANCE, AND REGULATION OF NA-PHOSPHATE COTRANSPORTER GENES IN MURINE KIDNEY()

      American journal of physiology. Renal, fluid and electrolyte physiology
    38. XIAO ZS; CRENSHAW M; GUO R; NESBITT T; DREZNER MK; QUARLES LD
      INTRINSIC MINERALIZATION DEFECT IN HYP MOUSE OSTEOBLASTS

      American journal of physiology: endocrinology and metabolism
    39. MULLER YL; COLLINS JF; GHISHAN FK
      GENETIC SCREENING FOR X-LINKED HYPOPHOSPHATEMIC MICE AND ONTOGENIC CHARACTERIZATION OF THE DEFECT IN THE RENAL SODIUM-PHOSPHATE TRANSPORTER

      Pediatric research
    40. ECONS MJ; FRIEDMAN NE; ROWE PSN; SPEER MC; FRANCIS F; STROM TM; OUDET C; SMITH JA; NINOMIYA JT; LEE BE; BERGEN H
      A PHEX GENE MUTATION IS RESPONSIBLE FOR ADULT-ONSET VITAMIN-D-RESISTANT HYPOPHOSPHATEMIC OSTEOMALACIA - EVIDENCE THAT THE DISORDER IS NOT ADISTINCT ENTITY FROM X-LINKED HYPOPHOSPHATEMIC RICKETS

      The Journal of clinical endocrinology and metabolism
    41. DIXON PH; CHRISTIE PT; WOODING C; TRUMP D; GRIEFF M; HOLM I; GERTNER JM; SCHMIDTKE J; SHAH B; SHAW N; SMITH C; TAU C; SCHLESSINGER D; WHYTE MP; THAKKER RV
      MUTATIONAL ANALYSIS OF PHEX GENE IN X-LINKED HYPOPHOSPHATEMIA

      The Journal of clinical endocrinology and metabolism
    42. SHIMOZAWA N; SUZUKI Y; ZHANG ZY; IMAMURA A; TSUKAMOTO T; OSUMI T; TATEISHI K; OKUMOTO K; FUJIKI Y; ORII T; BARTH PG; WANDERS RJA; KONDO N
      PEROXISOME BIOGENESIS DISORDERS - IDENTIFICATION OF A NEW COMPLEMENTATION GROUP DISTINCT FROM PEROXISOME-DEFICIENT CHO MUTANTS AND NOT COMPLEMENTED BY HUMAN PEX-13

      Biochemical and biophysical research communications
    43. ROWE PSN
      THE PEXGENE - ITS ROLE IN X-LINKED RICKETS, OSTEOMALACIA, AND BONE-MINERAL METABOLISM

      Experimental nephrology
    44. BAERENDS RJS; SALOMONS FA; FABER KN; KIEL JAKW; VANDERKLEI IJ; VEENHUIS M
      DEVIANT PEX3P LEVELS AFFECT NORMAL PEROXISOME FORMATION IN HANSENULA-POLYMORPHA - HIGH STEADY-STATE LEVELS OF THE PROTEIN FULLY ABOLISH MATRIX PROTEIN IMPORT

      Yeast


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 11/08/20 alle ore 21:14:47