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La ricerca find articoli where soggetti phrase all words 'FAMILIAL INTRAHEPATIC CHOLESTASIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 98 riferimenti
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    1. Schmitz, G; Kaminski, WE
      ABC transporters and cholesterol metabolism

      FRONTIERS IN BIOSCIENCE
    2. Dean, M; Rzhetsky, A; Allikmets, R
      The human ATP-binding cassette (ABC) transporter superfamily

      GENOME RESEARCH
    3. Schmitz, G; Langmann, T
      Structure, function and regulation of the ABC1 gene product

      CURRENT OPINION IN LIPIDOLOGY
    4. Hooiveld, GJEJ; van Montfoort, JE; Meijer, DKF; Muller, M
      Function and regulation of ATP-binding cassette transport proteins involved in hepatobiliary transport (vol 12, pg 13, 2000)

      EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
    5. Fischler, B; Papadogiannakis, N; Nemeth, A
      Clinical aspects on neonatal cholestasis based on observations at a Swedish tertiary referral centre

      ACTA PAEDIATRICA
    6. Fischler, B; Papadogiannakis, N; Nemeth, A
      Aetiological factors in neonatal cholestasis

      ACTA PAEDIATRICA
    7. Bassas, AF; Wali, SH; Chehab, MS; Al-Husseini, HF; Al-Shahed, MS; Al-Shuraffa, HA; Jawdat, MT
      Living-related liver transplantation

      SAUDI MEDICAL JOURNAL
    8. Jacquemin, E
      Role of multidrug resistance 3 deficiency in pediatric and adult liver disease: One gene for three diseases

      SEMINARS IN LIVER DISEASE
    9. Jansen, PLM; Muller, M; Sturm, E
      Genes and cholestasis

      HEPATOLOGY
    10. Schmitt, M; Kubitz, R; Lizun, S; Wettstein, M; Haussinger, D
      Regulation of the dynamic localization of the rat Bsep gene-encoded bile salt export pump by anisoosmolarity

      HEPATOLOGY
    11. Zollner, G; Fickert, P; Zenz, R; Fuchsbichler, A; Stumptner, C; Kenner, L; Ferenci, P; Stauber, RE; Krejs, GJ; Denk, H; Zatloukal, K; Trauner, M
      Hepatobiliary transporter expression in percutaneous liver biopsies of patients with cholestatic liver diseases

      HEPATOLOGY
    12. Trauner, M; Boyer, JL
      Cholestatic syndromes

      CURRENT OPINION IN GASTROENTEROLOGY
    13. Cai, SY; Wang, L; Ballatori, N; Boyer, JL
      Bile salt export pump is highly conserved during vertebrate evolution and its expression is inhibited by PFIC type II mutations

      AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
    14. Eppens, EF; van Mil, SWC; de Vree, JM; Mok, KS; Juijn, JA; Elferink, RPJO; Berger, R; Houwen, RHJ; Klomp, LWJ
      FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte

      JOURNAL OF HEPATOLOGY
    15. Stieger, B
      FIC1: another bile salt carrier within the enterohepatic circulation?

      JOURNAL OF HEPATOLOGY
    16. Oswald, M; Kullak-Ublick, GA; Paumgartner, G; Beuers, U
      Expression of hepatic transporters OATP-C and MRP2 in primary sclerosing cholangitis

      LIVER
    17. Dean, M; Hamon, Y; Chimini, G
      The human ATP-binding cassette (ABC) transporter superfamily

      JOURNAL OF LIPID RESEARCH
    18. St-Pierre, MV; Kullak-Ublick, GA; Hagenbuch, B; Meier, PJ
      Transport of bile acids in hepatic and non-hepatic tissues

      JOURNAL OF EXPERIMENTAL BIOLOGY
    19. Schuetz, EG; Strom, S; Yasuda, K; Lecureur, V; Assem, M; Brimer, C; Lamba, J; Kim, RB; Ramachandran, V; Komoroski, BJ; Venkataramanan, R; Cai, HB; Sinal, CJ; Gonzalez, FJ; Schuetz, JD
      Disrupted bile acid homeostasis reveals an unexpected interaction among nuclear hormone receptors, transporters, and cytochrome p450

      JOURNAL OF BIOLOGICAL CHEMISTRY
    20. Jacquemin, E; de Vree, JML; Cresteil, D; Sokal, EM; Sturm, E; Dumont, M; Scheffer, GL; Paul, M; Burdelski, M; Bosma, PJ; Bernard, O; Hadchouel, M; Elferink, RPJO
      The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood

      GASTROENTEROLOGY
    21. Ortiz, D; Arias, IM
      MDR3 mutations: A glimpse into pandora's box and the future of canalicularpathophysiology

      GASTROENTEROLOGY
    22. Lammert, F; Carey, MC; Paigen, B
      Chromosomal organization of candidate genes involved in cholesterol gallstone formation: A murine gallstone map

      GASTROENTEROLOGY
    23. Fattinger, K; Funk, C; Pantze, M; Weber, C; Reichen, J; Stieger, B; Meier, PJ
      The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: A potential mechanism for hepatic adverse reactions

      CLINICAL PHARMACOLOGY & THERAPEUTICS
    24. Wakusawa, S; Ikeda, R; Shiono, Y; Hayashi, H
      Protein kinase C-mediated down-regulation of MDR3 mRNA expression in Changliver cells

      BIOCHEMICAL PHARMACOLOGY
    25. Le Saux, O; Beck, K; Sachsinger, C; Silvestri, C; Treiber, C; Goring, HHH; Johnson, EW; De Paepe, A; Pope, FM; Pasquali-Ronchetti, I; Bercovitch, L; Terry, S; Boyd, CD
      A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticum

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Jansen, PLM
      The pathophysiology of cholestasis with special reference to primary biliary cirrhosis

      BEST PRACTICE & RESEARCH IN CLINICAL GASTROENTEROLOGY
    27. Borst, P; Zelcer, N; van Helvoort, A
      ABC transporters in lipid transport

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    28. Thompson, R; Strautnieks, S
      Inherited disorders of transport in the liver

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    29. Schmitz, G; Kaminski, WE; Orso, E
      ABC transporters in cellular lipid trafficking

      CURRENT OPINION IN LIPIDOLOGY
    30. Hooiveld, GJEJ; van Montfoort, JE; Meijer, DKF; Muller, M
      Function and regulation of ATP-binding cassette transport proteins involved in hepatobiliary transport

      EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
    31. Diaz, GJ
      Basolateral and canalicular transport of xenobiotics in the hepatocyte: A review

      CYTOTECHNOLOGY
    32. Jansen, PLM; Muller, M
      Genetic cholestasis: Lessons from the molecular physiology of bile formation

      CANADIAN JOURNAL OF GASTROENTEROLOGY
    33. Mourez, M; Jehanno, M; Hofnung, M; Dassa, E
      Role, functional mechanism and structure of ABC (ATP-binding cassette) transporters

      M S-MEDECINE SCIENCES
    34. Rebhandl, W; Felberbauer, FX; Huber, WD; Puig, S; Paya, K; Rauhofer, U; Saadi, S; Aberle, J; Horcher, E
      Progressive familial intrahepatic cholestasis (Byler disease): Current genetics and therapy

      KLINISCHE PADIATRIE
    35. Lecureur, V; Courtois, A; Payen, L; Verhnet, L; Guillouzo, A; Fardel, O
      Expression and regulation of hepatic drug and bile acid transporters

      TOXICOLOGY
    36. Drouin, E; Russo, P; Tuchweber, B; Mitchell, G; Rasquin-Weber, A
      North American Indian cirrhosis in children: A review of 30 cases

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    37. Ng, VL; Ryckman, FC; Porta, G; Miura, IK; de Carvalho, E; Servidoni, MF; Bezerra, JA; Balistreri, WF
      Long-term outcome after partial external biliary diversion for intractablepruritus in patients with intrahepatic cholestasis

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    38. Jansen, PLM
      Foreword: From classic bile physiology to cloned transporters

      SEMINARS IN LIVER DISEASE
    39. Kullak-Ublick, GA; Stieger, B; Hagenbuch, B; Meier, PJ
      Hepatic transport of bile salts

      SEMINARS IN LIVER DISEASE
    40. Elferink, RPJO; Groen, AK
      Mechanisms of biliary lipid secretion and their role in lipid homeostasis

      SEMINARS IN LIVER DISEASE
    41. Thompson, R; Jansen, PLM
      Genetic defects in hepatocanalicular transport

      SEMINARS IN LIVER DISEASE
    42. Lee, J; Boyer, JL
      Molecular alterations in hepatocyte transport mechanisms in acquired cholestatic liver disorders

      SEMINARS IN LIVER DISEASE
    43. Rigotti, A; Cohen, DE
      The Tangier disease gene encodes yet another pathophysiologically relevantATP-binding cassette protein

      HEPATOLOGY
    44. Dowling, RH
      Review: pathogenesis of gallstones

      ALIMENTARY PHARMACOLOGY & THERAPEUTICS
    45. Lefkowitch, JH
      Pathology of the liver

      CURRENT OPINION IN GASTROENTEROLOGY
    46. Trauner, M; Boyer, JL
      Cholestatic syndromes

      CURRENT OPINION IN GASTROENTEROLOGY
    47. Silva, ES; Lumbroso, S; Medina, M; Gillerot, Y; Sultan, C; Sokal, EM
      Demonstration of McCune-Albright mutations in the liver of children with high gamma GT progressive cholestasis

      JOURNAL OF HEPATOLOGY
    48. Elferink, RO; de Vree, M; Frijters, C; Groen, A
      The role of phospholipids in bile formation: What can we learn from animals and human disease?

      JOURNAL OF HEPATOLOGY
    49. Kullak-Ublick, GA; Beuers, U; Paumgartner, G
      Hepatobiliary transport

      JOURNAL OF HEPATOLOGY
    50. Poupon, R; Chazouilleres, O; Poupon, RE
      Chronic cholestatic diseases

      JOURNAL OF HEPATOLOGY
    51. Sinai, CJ; Tohkin, M; Miyata, M; Ward, JM; Lambert, G; Gonzalez, FJ
      Targeted disruption of the nuclear receptor FXR/BAR impairs bile acid and lipid homeostasis

      CELL
    52. Vleggaar, FP; Van Ooteghem, NAM; Van Buuren, HR; Henegouwen, GPV
      Cholestatic liver diseases: Slow progress in understanding and treating slowly progressive disorders

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    53. Klucken, J; Buchler, C; Orso, E; Kaminski, WE; Porsch-Ozcurumez, M; Liebisch, C; Kapinsky, M; Diederich, W; Drobnik, W; Dean, M; Allikmets, R; Schmitz, G
      ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    54. Smith, AJ; van Helvoort, A; van Meer, G; Szabo, K; Welker, E; Szakacs, G; Varadi, A; Sarkadi, B; Borst, P
      MDR3 P-glycoprotein, a phosphatidylcholine translocase, transports severalcytotoxic drugs and directly interacts with drugs as judged by interference with nucleotide trapping

      JOURNAL OF BIOLOGICAL CHEMISTRY
    55. Morton, DH; Salen, G; Batta, AK; Shefer, S; Tint, GS; Belchis, D; Shneider, B; Puffenberger, E; Bull, L; Knisely, AS
      Abnormal hepatic sinusoidal bile acid transport in an Amish kindred is notlinked to FIC1 and is improved by ursodiol

      GASTROENTEROLOGY
    56. Stieger, B; Fattinger, A; Madon, J; Kullak-Ublick, GA; Meier, PJ
      Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver

      GASTROENTEROLOGY
    57. Lee, JM; Trauner, M; Soroka, CJ; Stieger, B; Meier, PJ; Boyer, JL
      Expression of the bile salt export pump is maintained after chronic cholestasis in the rat

      GASTROENTEROLOGY
    58. Bull, LN; Roche, E; Song, EJ; Pedersen, J; Knisely, AS; van der Hagen, CB; Eiklid, K; Aagenaes, O; Freimer, NB
      Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q

      AMERICAN JOURNAL OF HUMAN GENETICS
    59. Betard, C; Rasquin-Weber, A; Brewer, C; Drouin, E; Clark, S; Verner, A; Darmond-Zwaig, C; Fortin, J; Mercier, J; Chagnon, P; Fujiwara, TM; Morgan, K; Richter, A; Hudson, TJ; Mitchell, GA
      Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22 - and identification of a shared haplotype

      AMERICAN JOURNAL OF HUMAN GENETICS
    60. Dinler, G; Kocak, N; Ozen, H; Yuce, A; Gurakan, F
      Ursodeoxycholic acid treatment in children with Byler disease

      PEDIATRICS INTERNATIONAL
    61. Rust, S; Rosier, M; Funke, H; Real, J; Amoura, Z; Piette, JC; Deleuze, JF; Brewer, HB; Duverger, N; Denefle, P; Assmann, G
      Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

      NATURE GENETICS
    62. Hardikar, W
      Genes for jaundice

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    63. Cohen, DE
      Hepatocellular transport and secretion of biliary lipids

      CURRENT OPINION IN LIPIDOLOGY
    64. Sauerbruch, T; Caselmann, WH; Spengler, U
      Hepatic disease

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    65. Bahar, RJ; Stolz, A
      Bile acid transport

      GASTROENTEROLOGY CLINICS OF NORTH AMERICA
    66. Elferink, RPJO; Groen, AK
      The mechanism of biliary lipid secretion and its defects

      GASTROENTEROLOGY CLINICS OF NORTH AMERICA
    67. Donovan, JM
      Physical and metabolic factors in gallstone pathogenesis

      GASTROENTEROLOGY CLINICS OF NORTH AMERICA
    68. Balistreri, WF
      Inborn errors of bile acid biosynthesis and transport - Novel forms of metabolic liver disease

      GASTROENTEROLOGY CLINICS OF NORTH AMERICA
    69. Kamisako, T; Gabazza, EC; Ishihara, T; Adachi, Y
      Molecular aspects of organic compound transport across the plasma membraneof hepatocytes

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    70. Bull, LN; Juijn, JA; Liao, M; van Eijk, MJT; Sinke, RJ; Stricker, NL; DeYoung, JA; Carlton, VEH; Baharloo, S; Klomp, LWJ; Abukawa, D; Barton, DE; Bass, NM; Bourke, B; Drumm, B; Jankowska, I; Lovisetto, P; McQuaid, S; Pawlowska, J; Tazawa, Y; Villa, E; Tygstrup, N; Berger, R; Knisely, AS; Houwen, RHJ; Freimer, NB
      Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC

      HUMAN GENETICS
    71. Shneider, BL
      Genetic cholestasis syndromes

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    72. Dranoff, JA; Nathanson, MH
      Regulation of bile acid transport: Beyond molecular cloning

      HEPATOLOGY
    73. Trauner, M; Graziadei, IW
      Review article: mechanisms of action and therapeutic applications of ursodeoxycholic acid in chronic liver diseases

      ALIMENTARY PHARMACOLOGY & THERAPEUTICS
    74. Trauner, M; Boyer, JL
      Cholestatic syndromes

      CURRENT OPINION IN GASTROENTEROLOGY
    75. Thompson, R
      Pediatric liver disease

      CURRENT OPINION IN GASTROENTEROLOGY
    76. Ortiz, DF; Li, SH; Iyer, R; Zhang, XM; Novikoff, P; Arias, IM
      MRP3, a new ATP-binding cassette protein localized to the canalicular domain of the hepatocyte

      AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
    77. Smith, AJ; Elferink, RPJO
      Liver gene disruptions: winners by KO?

      JOURNAL OF HEPATOLOGY
    78. Trauner, M; Meier, PJ; Boyer, JL
      Molecular regulation of hepatocellular transport systems in cholestasis

      JOURNAL OF HEPATOLOGY
    79. Trauner, M; Fickert, P; Stauber, RE
      New molecular aspects of cholestatic liver diseases

      ZEITSCHRIFT FUR GASTROENTEROLOGIE
    80. Oshima, T; Ikeda, K; Takasaka, T
      Sensorineural hearing loss associated with Byler disease

      TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
    81. Kim, RB; Leake, B; Cvetkovic, M; Roden, MM; Nadeau, J; Walubo, A; Wilkinson, GR
      Modulation by drugs of human hepatic sodium-dependent bile acid transporter (sodium taurocholate cotransporting polypeptide) activity

      JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
    82. Holve, S; Hu, D; Shub, M; Tyson, RW; Sokol, RJ
      Liver disease in Navajo neuropathy

      JOURNAL OF PEDIATRICS
    83. Holland, IB; Blight, MA
      ABC-ATPases, adaptable energy generators fuelling transmembrane movement of a variety of molecules organisms from bacteria to humans

      JOURNAL OF MOLECULAR BIOLOGY
    84. Klein, I; Sarkadi, B; Varadi, A
      An inventory of the human ABC proteins

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
    85. Burdelski, M; Rogiers, X
      Liver transplantation in metabolic disorders

      ACTA GASTRO-ENTEROLOGICA BELGICA
    86. POLEY JR; NOWICKI MJ
      OTHER HEREDITARY-DISEASES AND THE LIVER

      Bailliere's clinical gastroenterology
    87. KOOPEN NR; MULLER M; VONK RJ; ZIMNIAK P; KUIPERS F
      MOLECULAR MECHANISMS OF CHOLESTASIS - CAUSES AND CONSEQUENCES OF IMPAIRED BILE FORMATION

      Biochimica et biophysica acta. Molecular basis of disease
    88. MARTIN MG
      THE BIOLOGY OF INHERITED DISORDERS OF THE GASTROINTESTINAL-TRACT - PART II - PANCREATIC AND HEPATOBILIARY DISORDERS

      Journal of pediatric gastroenterology and nutrition
    89. MOSELEY RH
      WHAT THE AMISH CAN TELL US ABOUT - CHOLESTASIS

      Hepatology
    90. MULLER M; JANSEN PLM
      THE SECRETORY FUNCTION OF THE LIVER - NEW ASPECTS OF HEPATOBILIARY TRANSPORT

      Journal of hepatology
    91. ARRESE M; ANANTHANANARAYANAN M; SUCHY FJ
      HEPATOBILIARY TRANSPORT - MOLECULAR MECHANISMS OF DEVELOPMENT AND CHOLESTASIS

      Pediatric research
    92. TRAUNER M; MEIER PJ; BOYER JL
      MECHANISMS OF DISEASE - MOLECULAR PATHOGENESIS OF CHOLESTASIS

      The New England journal of medicine
    93. JACQUEMIN E; LYKAVIERIS P; CHAOUI N; HADCHOUEL M; BERNARD O
      TRANSIENT NEONATAL CHOLESTASIS - ORIGIN AND OUTCOME

      The Journal of pediatrics
    94. HOLLANDS CM; RIVERAPEDROGO FJ; GONZALEZVALLINA R; LORETDEMOLA O; NAHMAD M; BURNWEIT CA
      ILEAL EXCLUSION FOR BYLERS-DISEASE - AN ALTERNATIVE SURGICAL APPROACHWITH PROMISING EARLY RESULTS FOR PRURITUS

      Journal of pediatric surgery
    95. GERLOFF T; STIEGER B; HAGENBUCH B; MADON J; LANDMANN L; ROTH J; HOFMANN AF; MEIER PJ
      THE SISTER OF P-GLYCOPROTEIN REPRESENTS THE CANALICULAR BILE-SALT EXPORT PUMP OF MAMMALIAN LIVER

      The Journal of biological chemistry
    96. WIECHMANN DA; HEUBI JH
      PEDIATRIC HEPATOBILIARY DISEASE

      Current opinion in gastroenterology
    97. BRAEGGER CP; ALTORFER J
      ENDOSCOPIC BILIARY SPHINCTEROTOMY AND STONE EXTRACTION IN A CHILD WITH CHOLEDOCHOLITHIASIS COMPLICATING BYLERS DISEASE

      Journal of pediatric gastroenterology and nutrition
    98. MULLER G; VEYCKEMANS F; CARLIER M; VANOBBERGH LJ; DEKOCK M; SOKAL EM; OTTE JB
      ANESTHETIC CONSIDERATIONS IN PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS (BYLERS DISEASE)

      Canadian journal of anaesthesia


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Documento generato il 03/08/20 alle ore 17:42:00