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    1. Konrad, M; Wuthe, S; Meyer, F; Kaifer, E
      Dinucleating hybrid ligands providing a "soft" P boolean AND N and an adjacent N-rich coordination pocket - Controlled synthesis of unsymmetric homodinuclear and heterodinuclear complexes

      EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
    2. Roder, JC; Meyer, F; Konrad, M; Sandhofner, S; Kaifer, E; Pritzkow, H
      Difunctional pyrazole derivatives - Key compounds en route to multidentatepyrazolate ligands

      EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
    3. Konrad, M
      Conceiving persons: ethnographies of procreation, fertility and growth

      JOURNAL OF THE ROYAL ANTHROPOLOGICAL INSTITUTE
    4. Konrad, M
      Extending the boundaries of care: medical ethics & caring practices

      JOURNAL OF THE ROYAL ANTHROPOLOGICAL INSTITUTE
    5. Birkenhager, R; Otto, E; Schurmann, MJ; Vollmer, M; Ruf, EM; Maier-Lutz, I; Beekmann, F; Fekete, A; Omran, H; Feldmann, D; Milford, DV; Jeck, N; Konrad, M; Landau, D; Knoers, NVAM; Antignac, C; Sudbrak, R; Kispert, A; Hildebrandt, F
      Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

      NATURE GENETICS
    6. Weber, S; Schneider, L; Peters, M; Misselwitz, J; Ronnefarth, G; Boswald, M; Bonzel, KE; Seeman, T; Sulakova, T; Kuwertz-Broking, E; Gregoric, A; Palcoux, JB; Tasic, V; Manz, F; Scharer, K; Seyberth, HW; Konrad, M
      Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    7. Weber, S; Schlingmann, KP; Peters, M; Nejsum, LN; Nielsen, S; Engel, H; Grzeschik, KH; Seyberth, HW; Grone, HJ; Nusing, R; Konrad, M
      Primary gene structure and expression studies of rodent paracellin-1

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    8. Peters, M; Jeck, N; Seyberth, HW; Konrad, M
      Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes

      RARE KIDNEY DISEASES
    9. Jeck, N; Derst, C; Wischmeyer, E; Ott, H; Weber, S; Rudin, C; Seyberth, HW; Daut, J; Karschin, A; Konrad, M
      Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome

      KIDNEY INTERNATIONAL
    10. Rehse, N; Knoll, A; Konrad, M; Magerle, R; Krausch, G
      Surface reconstruction of an ordered fluid: An analogy with crystal surfaces - art. no. 035505

      PHYSICAL REVIEW LETTERS
    11. Jeck, N; Reinalter, SC; Henne, T; Marg, W; Mallmann, R; Pasel, K; Vollmer, M; Klaus, G; Leonhardt, A; Seyberth, HW; Konrad, M
      Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness

      PEDIATRICS
    12. Reinalter, SC; Grone, HJ; Konrad, M; Seyberth, HW; Klaus, G
      Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies

      JOURNAL OF PEDIATRICS
    13. Lecoq, K; Belloc, I; Desgranges, C; Konrad, M; Daignan-Fornier, B
      YLR209c encodes Saccharomyces cerevisiae purine nucleoside phosphorylase

      JOURNAL OF BACTERIOLOGY
    14. Erent, M; Gonin, P; Cherfils, J; Tissier, P; Raschella, G; Giartosio, A; Agou, F; Sarger, C; Lacombe, ML; Konrad, M; Lascu, I
      Structural and catalytic properties and homology modelling of the human nucleoside diphosphate kinase C, product of the DRnm23 gene

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    15. Maytum, R; Konrad, M; Lehrer, SS; Geeves, MA
      Regulatory properties of tropomyosin effects of length, isoform, and N-terminal sequence

      BIOCHEMISTRY
    16. Konrad, M; Vollmer, M; Lemmink, HH; Van den Heuvel, LPWJ; Jeck, N; Vargas-Poussou, R; Lakings, A; Ruf, R; Deschenes, G; Antignac, C; Guay-Woodford, L; Knoers, NVAM; Seyberth, HW; Feldmann, D; Hildebrandt, F
      Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    17. Weber, S; Hoffmann, K; Jeck, N; Saar, K; Boeswald, M; Kuwertz-Broeking, E; Meij, IIC; Knoers, NVAM; Cochat, P; Sulakova, T; Bonzel, KE; Soergel, M; Manz, F; Schaerer, K; Seyberth, HW; Reis, A; Konrad, M
      Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    18. Ostermann, N; Schlichting, I; Brundiers, R; Konrad, M; Reinstein, J; Veit, T; Goody, RS; Lavie, A
      Insights into the phosphoryltransfer mechanism of human thymidylate kinasegained from crystal structures of enzyme complexes along the reaction coordinate

      STRUCTURE WITH FOLDING & DESIGN
    19. Ptak, K; Konrad, M; Di Pasquale, E; Tell, F; Hilaire, G; Monteau, R
      Cellular and synaptic effect of substance P on neonatal phrenic motoneurons

      EUROPEAN JOURNAL OF NEUROSCIENCE
    20. Vollmer, M; Jeck, N; Lemmink, HH; Vargas, R; Feldmann, D; Konrad, M; Beekmann, F; van den Heuvel, LPWJ; Deschenes, G; Guay-Woodford, LM; Antignac, C; Seyberth, HW; Hildebrandt, F; Knoers, NVAM
      Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    21. Jeck, N; Konrad, M; Hess, M; Seyberth, HW
      The diuretic- and Bartter-like salt-losing tubulopathies

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    22. Weber, S; Soergel, M; Jeck, N; Konrad, M
      Atypical distal renal tubular acidosis confirmed by mutation analysis

      PEDIATRIC NEPHROLOGY
    23. Konrad, M
      Adopting a middle-class attitude of nobility for Jews in mid-nineteenth-century Hungary - Reinforcing opposition to the emancipation and social integration of Hungarian Jewry

      REVUE DES ETUDES JUIVES
    24. Jeck, N; Konrad, M; Peters, M; Weber, S; Bonzel, KE; Seyberth, HW
      Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

      PEDIATRIC RESEARCH
    25. Konrad, M; Knoll, A; Krausch, G; Magerle, R
      Volume imaging of an ultrathin SBS triblock copolymer film

      MACROMOLECULES
    26. Ostermann, N; Lavie, A; Padiyar, S; Brundiers, R; Veit, T; Reinstein, J; Goody, RS; Konrad, M; Schlichting, I
      Potentiating AZT activation: Structures of wild-type and mutant human thymidylate kinase suggest reasons for the mutants' improved kinetics with the HIV prodrug metabolite AZTMP

      JOURNAL OF MOLECULAR BIOLOGY
    27. Lecoq, K; Konrad, M; Daignan-Fornier, B
      Yeast GMP kinase mutants constitutively express AMP biosynthesis genes by phenocopying a hypoxanthine-guanine phosphoribosyltransferase defect

      GENETICS
    28. Kumar, V; Spangenberg, O; Konrad, M
      Cloning of the guanylate kinase homologues ACK-1 and AGK-2 from Arabidopsis thaliana and characterization of AGK-1

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    29. Maytum, R; Geeves, MA; Konrad, M
      Actomyosin regulatory properties of yeast tropomyosin are dependent upon N-terminal modification

      BIOCHEMISTRY
    30. Jeck, N; Konrad, M; Seyberth, HW
      Hereditary hypokalemic salt-losing tubulopathies

      CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS
    31. Meyer, F; Konrad, M; Kaifer, E
      Novel mu(3)-coordination of urea at a nickel(II) site: Structure, reactivity and ferromagnetic superexchange

      EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
    32. Konrad, M; Pavlik, V; Mares, P
      Kainic acid increases activity only of some cortical neurons in the rat.

      PHYSIOLOGICAL RESEARCH
    33. Gebhardt, RP; Konrad, M
      Comparison of need for care of sheltered home residents and patients of anambulant care unit

      PSYCHIATRISCHE PRAXIS
    34. Loble, M; Goller-Martin, S; Roth, B; Konrad, M; Bernhard, A; Naumann, A; Felbel, D
      Family foster care for adolescents with mental disorders

      PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE
    35. Konrad, M; Leonhardt, A; Hensen, P; Seyberth, HW; Kockerling, A
      Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes

      PEDIATRICS
    36. Schulte, U; Hahn, H; Konrad, M; Jeck, N; Derst, C; Wild, K; Weidemann, S; Ruppersberg, JP; Fakler, B; Ludwig, J
      pH gating of ROMK (K(ir)1.1) channels: Control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    37. Brundiers, R; Lavie, A; Veit, T; Reinstein, J; Schlichting, I; Ostermann, N; Goody, RS; Konrad, M
      Modifying human thymidylate kinase to potentiate azidothymidine activation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    38. Prinz, H; Lavie, A; Scheidig, AJ; Spangenberg, O; Konrad, M
      Binding of nucleotides to guanylate kinase, p21(ras), and nucleoside-diphosphate kinase studied by nano-electrospray mass spectrometry

      JOURNAL OF BIOLOGICAL CHEMISTRY
    39. Schaertl, S; Geeves, MA; Konrad, M
      Human nucleoside diphosphate kinase B (Nm23-82) from melanoma cells shows altered phosphoryl transfer activity due to the S122P mutation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    40. Konrad, M; Meyer, F; Jacobi, A; Kircher, P; Rutsch, P; Zsolnai, L
      Coordination and conversion of urea at dinuclear mu-acetato nickel(II) complexes with symmetric and asymmetric cores

      INORGANIC CHEMISTRY
    41. Hesse, S; Konrad, M; Uhlenbrock, D
      Treadmill walking with partial body weight support versus floor walking inhemiparetic subjects

      ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
    42. Konrad, M
      Ova donation and symbols of substance: Some variations on the theme of sex, gender and the partible body

      JOURNAL OF THE ROYAL ANTHROPOLOGICAL INSTITUTE
    43. LAVIE A; REINSTEIN J; GOODY RS; SCHLICHTING I; KONRAD M
      IMPROVING AZT EFFICACY - REPLY

      Nature medicine
    44. KONRAD M; SAUNIER S; CALADO J; GUBLER MC; BROYER M; ANTIGNAC C
      FAMILIAL JUVENILE NEPHRONOPHTHISIS

      Journal of molecular medicine
    45. Hesse, S; Jahnke, MT; Schaffrin, A; Lucke, D; Reiter, F; Konrad, M
      Immediate effects of therapeutic facilitation on the gait of hemiparetic patients as compared with walking with and without a cane

      ELECTROMYOGRAPHY AND MOTOR CONTROL-ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY
    46. KONRAD M; MEYER F; HEINZE K; ZSOLNAI L
      UNSYMMETRICALLY SUBSTITUTED PYRAZOLATES - NICKEL(II) COMPLEXES OF A NOVEL DINUCLEATING LIGAND PROVIDING BOTH N-RICH AND S-RICH COORDINATIONSPHERES

      Journal of the Chemical Society. Dalton transactions
    47. HESSE S; REITER F; KONRAD M; JAHNKE MT
      BOTULINUM TOXIN TYPE-A AND SHORT-TERM ELECTRICAL-STIMULATION IN THE TREATMENT OF UPPER-LIMB FLEXOR SPASTICITY AFTER STROKE - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL

      Clinical rehabilitation
    48. JECK N; KONRAD M; WEBER S; REINALTER S; SEYBERTH HW
      MUTATIONS IN CLCKB-CHANNEL CAUSE BARTTER-SYNDROME

      Naunyn-Schmiedeberg's archives of pharmacology
    49. LAVIE A; OSTERMANN N; BRUNDIERS R; GOODY RS; REINSTEIN J; KONRAD M; SCHLICHTING I
      STRUCTURAL BASIS FOR EFFICIENT PHOSPHORYLATION OF 3'-AZIDOTHYMIDINE MONOPHOSPHATE BY ESCHERICHIA-COLI THYMIDYLATE KINASE

      Proceedings of the National Academy of Sciences of the United Statesof America
    50. DERST C; WISCHMEYER E; PREISIGMULLER R; SPAUSCHUS A; KONRAD M; HENSEN P; JECK N; SEYBERTH HW; DAUT J; KARSCHIN A
      A HYPERPROSTAGLANDIN-E SYNDROME MUTATION IN KIR1.1 (RENAL OUTER MEDULLARY POTASSIUM) CHANNELS REVEALS A CRUCIAL RESIDUE FOR CHANNEL FUNCTION IN KIR1.3 CHANNELS

      The Journal of biological chemistry
    51. SCHAERTL S; KONRAD M; GEEVES MA
      SUBSTRATE-SPECIFICITY OF HUMAN NUCLEOSIDE-DIPHOSPHATE KINASE REVEALEDBY TRANSIENT KINETIC-ANALYSIS

      The Journal of biological chemistry
    52. KUHLENDAHL S; SPANGENBERG O; KONRAD M; KIM E; GARNER CC
      FUNCTIONAL-ANALYSIS OF THE GUANYLATE KINASE-LIKE DOMAIN IN THE SYNAPSE-ASSOCIATED PROTEIN SAP97

      European journal of biochemistry
    53. MAYTUM R; KONRAD M; GEEVES MA
      EFFECT OF N-TERMINAL MUTATIONS ON THE PROPERTIES OF YEAST TROPOMYOSIN-1

      Biophysical journal
    54. LAVIE A; KONRAD M; BRUNDIERS R; GOODY RS; SCHLICHTING I; REINSTEIN J
      CRYSTAL-STRUCTURE OF YEAST THYMIDYLATE KINASE COMPLEXED WITH THE BISUBSTRATE INHIBITOR P-1-(5'-ADENOSYL) P-5-(5'-THYMIDYL) PENTAPHOSPHATE (TP(5)A) AT 2.0-ANGSTROM RESOLUTION - IMPLICATIONS FOR CATALYSIS AND AZT ACTIVATION

      Biochemistry
    55. VARGASPOUSSOU R; FELDMANN D; VOLLMER M; KONRAD M; KELLY L; VANDENHEUVEL LPWJ; TEBOURBI L; BRANDIS M; KAROLYI L; HEBERT SC; LEMMINK HH; DESCHENES G; HILDEBRANDT F; SEYBERTH HW; GUAYWOODFORD LM; KNOERS NVAM; ANTIGNAC C
      NOVEL MOLECULAR VARIANTS OF THE NA-K-2CL COTRANSPORTER GENE ARE RESPONSIBLE FOR ANTENATAL BARTTER-SYNDROME

      American journal of human genetics
    56. LAVIE A; SCHLICHTING I; VETTER IR; KONRAD M; REINSTEIN J; GOODY RS
      THE BOTTLENECK IN AZT ACTIVATION

      Nature medicine
    57. LAVIE A; VETTER IR; KONRAD M; GOODY RS; REINSTEIN J; SCHLICHTING I
      STRUCTURE OF THYMIDYLATE KINASE REVEALS THE CAUSE BEHIND THE LIMITINGSTEP IN AZT ACTIVATION

      Nature structural biology
    58. KONRAD M; KOCKERLING A; LEONHARDT A; KAROLYI L; SEYBERTH HW
      PRE-NATAL AND POSTNATAL MANAGEMENT OF HYPERPROSTAGLANDIN-E SYNDROME (HPS) FOLLOWING MOLECULAR-GENETIC DIAGNOSIS FROM AMNIOCYTES

      Journal of the American Society of Nephrology
    59. KONRAD M; HENSEN P; KAROLYI L; SEYBERTH HW
      NOVEL ROMK (KCNJ1) MUTATIONS IN 2 SPORADIC CASES WITH HYPERPROSTAGLANDIN-E SYNDROME (ANTENATAL BARTTER-SYNDROME)

      Journal of the American Society of Nephrology
    60. KAROLYI L; KONRAD M; KOCKERLING A; ZIEGLER A; ZIMMERMANN DK; ROTH B; WIEG C; GRZESCHIK KH; KOCH MC; SEYBERTH HW; VARGAS R; FORESTIER L; JEAN G; DESCHAUX M; RIZZONI GF; NIAUDET P; ANTIGNAC C; FELDMANN D; LORRIDON F; COUGOUREUX E; LAROZE F; ALESSANDRI JL; DAVID L; SAUNIER P; DESCHENES G; HILDEBRANDT F; VOLLMER M; PROESMANS W; BRANDIS M; VANDENHEUVEL LPWJ; LEMMINK HH; NILLESEN W; MONNENS LAH; KNOERS NVAM; GUAYWOODFORD LM; WRIGHT CJ; MADRIGAL G; HEBERT SC
      MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997)

      Human molecular genetics
    61. SAUNIER S; CALADO J; HEILIG R; SILBERMANN F; BENESSY F; MORIN G; KONRAD M; BROYER M; GUBLER MC; WEISSENBACH J; ANTIGNAC C
      A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS

      Human molecular genetics
    62. KAROLYI L; KONRAD M; KOCKERLING A; ZIEGLER A; ZIMMERMANN DK; ROTH B; WIEG C; GRZESCHIK KH; KOCH MC; SEYBERTH HW; VARGAS R; FORESTIER L; JEAN G; DESCHAUX M; RIZZONI GF; NIAUDET P; ANTIGNAC C; FELDMANN D; LORRIDON F; COUGOUREUX E; LAROZE F; ALESSANDRI JL; DAVID L; SAUNIER P; DESCHENES G; HILDEBRANDT F; VOLLMER M; PROESMANS W; BRANDIS M; VANDENHEUVEL LPJ; LEMMINK HH; NILLESEN W; MONNENS LAH; KNOERS NVAM; GUAYWOODFORD LM; WRIGHT CJ; MADRIGAL G; HEBERT SC
      MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY

      Human molecular genetics
    63. SEEMAN T; SIKUT M; KONRAD M; VONDRICHOVA H; JANDA J; SCHARER K
      BLOOD-PRESSURE AND RENAL-FUNCTION IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE

      Pediatric nephrology
    64. HAEFFNER A; ABBAL M; MYTILINEOS J; KONRAD M; KRAMMER I; BOUISSOU F; OPELZ G; SCHARER K; CAMBONTHOMSEN A
      OLIGOTYPING FOR HLA-DQA, HLA-DQB, AND HLA-DPB IN IDIOPATHIC NEPHROTICSYNDROME

      Pediatric nephrology
    65. KONRAD M; MYTILINEOS J; RUDER H; OPELZ G; SCHARER K
      HLA-DR7 PREDICTS THE RESPONSE TO ALKYLATING-AGENTS IN STEROID-SENSITIVE NEPHROTIC SYNDROME

      Pediatric nephrology
    66. DANIEL V; TRAUTMANN Y; KONRAD M; NAYIR A; SCHARER K
      T-LYMPHOCYTE POPULATIONS, CYTOKINES AND OTHER GROWTH-FACTORS IN SERUMAND URINE OF CHILDREN WITH IDIOPATHIC NEPHROTIC SYNDROME

      Clinical nephrology
    67. BITTL X; ECKARDT V; FESSLER H; GONG WG; KONRAD M; MOCK A; ODIAN A; SEYBOTH P; DRAPER JE; HILDEBRANDT M; NESS K; SCHMIDT B
      DIFFUSION AND DRIFT STUDIES OF AR-DME CO2/CH4 GAS-MIXTURES FOR A RADIAL TPC IN THE E-PERPENDICULAR-TO-B FIELD/

      Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment
    68. HRABOVSKY M; KONRAD M; KOPECKY V; SEMBER V
      PROCESSES AND PROPERTIES OF ELECTRIC-ARC STABILIZED BY WATER VORTEX

      IEEE transactions on plasma science
    69. HECKMANN M; KONZ B; ZOGELMEIER F; KONRAD M; PLEWIG G
      DISCORDANCE OF UV-EXPOSURE AND FREQUENCY OF BASAL-CELL CARCINOMA

      Journal of investigative dermatology
    70. LASCU I; SCHAERTL S; WANG CQ; SARGER C; GIARTOSIO A; BRIAND G; LACOMBE ML; KONRAD M
      A POINT MUTATION OF HUMAN NUCLEOSIDE DIPHOSPHATE KINASE-A FOUND IN AGGRESSIVE NEUROBLASTOMA AFFECTS PROTEIN-FOLDING

      The Journal of biological chemistry
    71. CURTIS B; HEFLEY WE; MILLER S; KONRAD M
      DEVELOPING ORGANIZATIONAL COMPETENCE

      Computer
    72. UHLENBROCK D; SARKODIEGYAN T; REITER F; KONRAD M; HESSE S
      DEVELOPMENT OF A SERVO-CONTROLLED GAIT TR AINER FOR THE REHABILITATION OF NON-AMBULATORY PATIENTS

      Biomedizinische Technik
    73. KONRAD M; MEYER F; BUCHNER M; HEINZE K; ZSOLNAI L
      DIMERIC SILVER(I) COMPLEXES OF SOME ISOTHIAZOLE-BASED LIGANDS

      Chemische Berichte
    74. SCHAERTL S; KONRAD M; LASCU I; GEEVES MA
      TRANSIENT KINETIC-STUDIES OF PHOSPHATE-TRANSFER REACTIONS IN HUMAN-BETA NUCLEOSIDE DIPHOSPHATE KINASE

      Biophysical journal
    75. DERST C; KONRAD M; KOCKERLING A; KAROLYI L; DESCHENES G; DAUT J; KARSCHIN A; SEYBERTH HW
      MUTATIONS IN THE ROMK GENE IN ANTENATAL BARTTER-SYNDROME ARE ASSOCIATED WITH IMPAIRED K+ CHANNEL FUNCTION

      Biochemical and biophysical research communications
    76. CALADO J; SAUNIER S; KONRAD M; BENESSY F; SILBERMANN F; ECKART P; NIAUDET P; BROYER M; ANTIGNAC C
      MOLECULAR DIAGNOSIS - A SUBSTITUTE FOR RENAL BIOPSY IN NEPHRONOPHTHISIS

      Journal of the American Society of Nephrology
    77. KONRAD M; SAUNIER S; HEIDET L; SILBERMANN F; BENESSY F; CALADO J; LEPASLIER D; BROYER M; GUBLER MC; ANTIGNAC C
      LARGE HOMOZYGOUS DELETIONS OF THE 2Q13 REGION ARE A MAJOR CAUSE OF JUVENILE NEPHRONOPHTHISIS

      Human molecular genetics
    78. ZERRES K; RUDNIKSCHONEBORN S; DEGET F; HOLTKAMP U; BRODEHL J; GEISERT J; SCHARER K; RUDER H; RASCHER W; DIPPEL J; HUFSCHMIDT C; MULLERWIEFEL DE; KONRAD M; KAARIAINEN H; MISSELWITZ J; VOLPEL S; MICHALK D; EIFE R; KUWERTZBROCKING E; VONMUHLENDAHL KE
      AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE IN 115 CHILDREN - CLINICAL PRESENTATION, COURSE AND INFLUENCE OF GENDER

      Acta paediatrica
    79. KONRAD M; MERZ WE
      LONG-TERM EFFECT OF CYCLIC-AMP ON N-GLYCOSYLATION IS CAUSED BY AN INCREASE IN THE ACTIVITY OF THE CIS-PRENYLTRANSFERASE

      Biochemical journal
    80. GIARTOSIO A; ERENT M; CERVONI L; MORERA S; JANIN J; KONRAD M; LASCU I
      THERMAL-STABILITY OF HEXAMERIC AND TETRAMERIC NUCLEOSIDE DIPHOSPHATE KINASES - EFFECT OF SUBUNIT INTERACTION

      The Journal of biological chemistry
    81. KONRAD M; SAUNIER S; SILBERMANN F; BENESSY F; GUBLER MC; ANTIGNAC C
      PHYSICAL MAP OF THE NEPHRONOPHTHISIS REGION - EXCLUSION OF PAX8 AS A POSSIBLE CANDIDATE GENE

      Journal of the American Society of Nephrology
    82. KONRAD M; SAUNIER S; SILBERMANN F; BENESSY F; LEPASLIER D; WEISSENBACH J; BROYER M; GUBLER MC; ANTIGNAC C
      A 11 MB YAC-BASED CONTIG SPANNING THE FAMILIAL JUVENILE NEPHRONOPHTHISIS REGION (NPH1) LOCATED ON CHROMOSOME 2Q

      Genomics
    83. KONRAD M; ZERRES K; WUHL E; RUDNIKSCHONEBORN S; HOLTKAMP U; SCHARER K
      BODY GROWTH IN CHILDREN WITH POLYCYSTIC KIDNEY-DISEASE

      Acta paediatrica
    84. BOUISSOU F; MEISSNER I; KONRAD M; SOMMER E; MYTILINEOS J; OHAYON E; SIERP G; BARTHE B; OPELZ G; CAMBONTHOMSEN A; SCHARER K
      CLINICAL IMPLICATIONS FROM STUDIES OF HLA ANTIGENS IN IDIOPATHIC NEPHROTIC SYNDROME IN CHILDREN

      Clinical nephrology
    85. KONRAD M
      MANUFACTURING BABIES AND PUBLIC CONSENT - DEBATING THE NEW REPRODUCTIVE TECHNOLOGIES - VANDYCK,J

      Sociology
    86. KONRAD M; MYTILINEOS J; BOUISSOU F; MEISSNER I; CAMBONTHOMSEN A; RUDER H; OPELZ G; SCHARER K
      IMMUNOGENETIC STUDIES IN IDIOPATHIC NEPHR OTIC SYNDROME IN CHILDREN -CLINICAL IMPLICATION OF HLA TYPING

      Monatsschrift fur Kinderheilkunde
    87. KONRAD M; SAUNIER S; SILBERMANN F; BENESSY F; GUBLER MC; ANTIGNAC C
      A 11 MB YAC BASED CONTIG SPANNING THE FAMILIAL JUVENILE NEPHRONOPHTHISIS REGION (NPH1) LOCATED ON CHROMOSOME 2Q

      American journal of human genetics
    88. SAUNIER S; BENESSY F; CHEVET D; SIMON P; SILBERMANN F; KONRAD M; HABIB R; ANTIGNAC C
      LINKAGE ANALYSIS IN FAMILIAL INTERSTITIAL NEPHRITIS

      Journal of the American Society of Nephrology
    89. KONRAD M; JAEGGI C; STURZENEGGER M; VALACH L
      THE CHARACTERISTICS OF YOUNG SUICIDE ATTE MPTERS AND THEIR IMPLICATIONS FOR HELPERS

      PPmP. Psychotherapie, Psychosomatik, medizinische Psychologie
    90. KONRAD M; MERZ WE
      REGULATION OF N-GLYCOSYLATION - LONG-TERM EFFECT OF CYCLIC-AMP MEDIATES ENHANCED SYNTHESIS OF THE DOLICHOL PYROPHOSPHATE CORE OLIGOSACCHARIDE

      The Journal of biological chemistry
    91. KONRAD M; MYTILINEOS J; BOUISSOU F; SCHERER S; GULLI MP; MEISSNER I; CAMBONTHOMSEN A; OPELZ G; SCHARER K
      HLA CLASS-II ASSOCIATIONS WITH IDIOPATHIC NEPHROTIC SYNDROME IN CHILDREN

      Tissue antigens
    92. CHAO FC; KIM BB; HOURANIEH AM; LIANG FH; TULLIS JL; SWISHER SN; KONRAD M
      INFUSIBLE PLATELET MEMBRANE (IPM) IS A POTENTIAL SUBSTITUTE FOR PLATELETS IN TRANSFUSION - CORRECTION OF PROLONGED BLEEDING-TIME IN THROMBOCYTOPENIC RABBITS

      Thrombosis and haemostasis
    93. ENZMANN PJ; KONRAD M; PAREY K
      VHS IN WILD LIVING FISH AND EXPERIMENTAL TRANSMISSION OF THE VIRUS

      Fisheries research
    94. KONRAD M
      MOLECULAR ANALYSIS OF THE ESSENTIAL GENE FOR ADENYLATE KINASE FROM THE FISSION YEAST SCHIZOSACCHAROMYCES-POMBE

      The Journal of biological chemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 15:11:04