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    1. Israel, FP; Baas, F
      CI and CO in the spiral galaxies NGC 6946 and M 83

      ASTRONOMY & ASTROPHYSICS
    2. Ten Asbroek, ALMA; Olsen, J; Housman, D; Baas, F; Stanton, V
      Genetic variation in mRNA coding sequences of highly conserved genes

      PHYSIOLOGICAL GENOMICS
    3. van Kuilenburg, ABP; Muller, EW; Haasjes, J; Meinsma, R; Zoetekouw, L; Waterham, HR; Baas, F; Richel, DJ; van Gennip, AH
      Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: Frequency of thecommon IVS14+1G > A mutation causing DPD deficiency

      CLINICAL CANCER RESEARCH
    4. van Deutekom, JCT; Bremmer-Bout, M; Janson, AAM; Ginjaar, IB; Baas, F; den Dunnen, JT; van Ommen, GJB
      Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells

      HUMAN MOLECULAR GENETICS
    5. De Jonge, RR; Van Schaik, IN; Vermeulen, M; Kwa, MSG; Baas, F
      cAMP is involved in the differentiation of human teratocarcinoma cells

      NEUROSCIENCE LETTERS
    6. Kwa, MSG; van Schaik, IN; Brand, A; Baas, F; Vermeulen, M
      Investigation of serum response to PMP22, connexin 32 and P-0 in inflammatory neuropathies

      JOURNAL OF NEUROIMMUNOLOGY
    7. Caron, H; van Schaik, B; van der Mee, M; Baas, F; Riggins, G; van Sluis, P; Hermus, MC; van Asperen, R; Boon, K; Voute, PA; Heisterkamp, S; van Kampen, A; Versteeg, R
      The human transcriptome map: Clustering of highly expressed genes in chromosomal domains

      SCIENCE
    8. Veldink, JH; van den Berg, LH; Cobben, JM; Stulp, RP; De Jong, JMBV; Vogels, OJ; Baas, F; Wokke, JHJ; Scheffer, H
      Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS

      NEUROLOGY
    9. Vandeputte, DAA; Meije, CB; van Dartel, M; Leenstra, S; IJlst-Keizers, H; Das, PK; Troost, D; Bosch, DA; Baas, F; Hulsebos, TJM
      GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    10. van Kampen, AHC; van Schaik, BDC; Pauws, E; Michiels, EMC; Ruijter, JM; Caron, HN; Versteeg, R; Heisterkamp, SH; Leunissen, JAM; Baas, F; van der Mee, M
      USAGE: a web-based approach towards the analysis of SAGE data

      BIOINFORMATICS
    11. Bergen, AAB; Plomp, AS; Schuurman, EJ; Terry, S; Breuning, M; Dauwerse, H; Swart, J; Kool, M; van Soest, S; Baas, F; ten Brink, JB; de Jong, PTVM
      Mutations in ABCC6 cause pseudoxanthoma elasticum

      NATURE GENETICS
    12. Muchir, A; Bonne, G; van der Kool, AJ; van Meegen, M; Baas, F; Bolhuis, PA; de Visser, M; Schwartz, K
      Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

      HUMAN MOLECULAR GENETICS
    13. Scheper, W; Zwart, R; van der Sluijs, P; Annaert, W; van Gool, WA; Baas, F
      Alzheimer's presenilin 1 is a putative membrane receptor for rab GDP dissociation inhibitor

      HUMAN MOLECULAR GENETICS
    14. Chandler, D; Angelicheva, D; Heather, L; Gooding, R; Gresham, D; Yanakiev, P; de Jonge, R; Baas, F; Dye, D; Karagyozov, L; Savov, A; Blechschmidt, K; Keats, B; Thomas, PK; King, RHM; Starr, A; Nikolova, A; Colomer, J; Ishpekova, B; Tournev, I; Urtizberea, JA; Merlini, L; Butinar, D; Chabrol, B; Voit, T; Baethmann, M; Nedkova, V; Corches, A; Kalaydjieva, L
      Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

      NEUROMUSCULAR DISORDERS
    15. ten Asbroek, ALMA; Fluiter, K; van Groenigen, M; Nooij, M; Baas, F
      Polymorphisms in the large subunit of human RNA polymerase II as target for allele-specific inhibition

      NUCLEIC ACIDS RESEARCH
    16. Lemstra, AW; van Meegen, MT; Vreyling, JP; Meijerink, PHS; Jansen, GH; Bulk, S; Baas, F; van Gool, WA
      14-3-3 testing in diagnosing Creutzfeldt-Jakob disease - A prospective study in 112 patients

      NEUROLOGY
    17. Wijnholds, J; Mol, CAAM; van Deemter, L; de Haas, M; Scheffer, GL; Baas, F; Beijnen, JH; Scheper, RJ; Hatse, S; De Clercq, E; Balzarini, J; Borst, P
      Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogs

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    18. Pauws, E; Moreno, JC; Tijssen, M; Baas, F; De Vijlder, JJM; Ris-Stalpers, C
      Serial analysis of gene expression as a tool to assess the human thyroid expression profile and to identify novel thyroidal genes

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    19. Kalaydjieva, L; Gresham, D; Gooding, R; Heather, L; Baas, F; de Jonge, R; Blechschmidt, K; Angelicheva, D; Chandler, D; Worsley, P; Rosenthal, A; King, RHM; Thomas, PK
      N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom

      AMERICAN JOURNAL OF HUMAN GENETICS
    20. Michiels, EMC; Oussoren, E; Van Groenigen, M; Pauws, E; Bossuyt, PMM; Voute, PA; Baas, F
      Genes differentially expressed in medulloblastoma and fetal brain

      PHYSIOLOGICAL GENOMICS
    21. Grierson, AJ; van Groenigen, M; Groot, NPB; Lindblad, K; Hoovers, JMN; Schalling, M; de Belleroche, J; Baas, F
      An integrated map of chromosome 18 CAG trinucleotide repeat loci

      EUROPEAN JOURNAL OF HUMAN GENETICS
    22. Groenewegen, MAT; Baas, F; Blommaert, JADL; Stehle, R; Josselin, E; Tilanus, RPJ
      Millimeter and some near infra-red observations of short-period Miras and other AGB stars

      ASTRONOMY & ASTROPHYSICS SUPPLEMENT SERIES
    23. Hafezparast, M; Witherden, A; Nicholson, S; Bermingham, N; Mackin, J; ten Asbroek, A; Ball, S; Peters, J; Baas, F; Martin, JE; Fisher, EMC
      The kinesin light chain gene: its mapping and exclusion in mouse and humanforms of inherited motor neuron degeneration

      NEUROSCIENCE LETTERS
    24. Barth, PG; Wanders, RJA; Vreken, P; Janssen, EAM; Lam, J; Baas, F
      X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

      JOURNAL OF INHERITED METABOLIC DISEASE
    25. Skinner, CJ; Justtanont, K; Tielens, AGGM; Betz, AL; Boreiko, RT; Baas, F
      Modelling the dust and gas outflows from IRC+10 216 - I. Ground-based and airborne observations

      MONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY
    26. Kool, M; van der Linden, M; de Haas, M; Scheffer, GL; de Vree, JML; Smith, AJ; Jansen, G; Peters, GJ; Ponne, N; Scheper, RJ; Elferink, RPJO; Baas, F; Borst, P
      MRP3, an organic anion transporter able to transport anti-cancer drugs

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    27. Kool, M; van der Linden, M; de Haas, M; Baas, F; Borst, P
      Expression of human MRP6, a homologue of the multidrug resistance protein gene MRP1, in tissues and cancer cells

      CANCER RESEARCH
    28. Sandell, G; Avery, LW; Baas, F; Coulson, I; Dent, WRF; Friberg, P; Gear, WPK; Greaves, J; Holland, W; Jenness, T; Jewell, P; Lightfoot, J; Matthews, HE; Moriarty-Schieven, G; Prestage, R; Robson, EI; Stevens, J; Tilanus, RPJ; Watt, GD
      A jet-driven, extreme high-velocity outflow powered by a cold, low-luminosity protostar near NGC 2023

      ASTROPHYSICAL JOURNAL
    29. Israel, FP; Baas, F
      Molecular gas in the bulge and ring of NGC 7331

      ASTRONOMY AND ASTROPHYSICS
    30. LINSSEN WHJP; DEVISSER M; NOTERMANS NC; VREYLING JP; VANDOORN PA; WOKKE JHJ; BAAS F; BOLHUIS PA
      GENETIC-HETEROGENEITY IN MIYOSHI-TYPE DISTAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    31. Baas, F
      Genomic studies of expanded unstable trinucleotide sequences in relation to heritable disorders

      HUMAN GENOME ANALYSIS
    32. WIKSTROM L; JOHANSSON C; SALTO C; BARLOW C; BARROS AC; BAAS F; FORREST D; THOREN P; VENNSTROM B
      ABNORMAL HEART-RATE AND BODY-TEMPERATURE IN MICE LACKING THYROID-HORMONE RECEPTOR ALPHA-1

      EMBO journal
    33. EVERS R; KOOL M; VANDEEMTER L; JANSSEN H; CALAFAT J; OOMEN LCJM; PAULUSMA CC; ELFERINK RPJO; BAAS F; SCHINKEL AH; BORSI P
      DRUG EXPORT ACTIVITY OF THE HUMAN CANALICULAR MULTISPECIFIC ORGANIC ANION TRANSPORTER IN POLARIZED KIDNEY MDCK CELLS EXPRESSING CMOAT (MRP2) CDNA

      The Journal of clinical investigation
    34. MEIJERINK PHS; YANAKIEV P; ZORN I; GRIERSON AJ; BIKKER H; DYE D; KALAYDJIEVA L; BAAS F
      THE GENE FOR THE HUMAN SRC-LIKE ADAPTER PROTEIN (HSLAP) IS LOCATED WITHIN THE 64-KB INTRON OF THE THYROGLOBULIN GENE

      European journal of biochemistry
    35. ISRAEL FP; TILANUS RPJ; BAAS F
      DETECTION OF NEUTRAL CARBON IN THE M-31 DARK CLOUD D-478

      Astronomy and astrophysics (Berlin)
    36. MOTLEY AM; HETTEMA EH; HOGENHOUT EM; BRITES P; TENASBROEK ALMA; WIJBURG FA; BAAS F; HEIJMANS HS; TABAK HF; WANDERS RJA; DISTEL B
      RHIZOMELIC CHONDRODYSPLASIA PUNCTATA IS A PEROXISOMAL PROTEIN TARGETING DISEASE CAUSED BY A NONFUNCTIONAL PTS2 RECEPTOR

      Nature genetics
    37. VISSER M; SIJMONS C; BRAS J; ARCECI RJ; GODFRIED M; VALENTIJN LJ; VOUTE PA; BAAS F
      ALLELOTYPE OF PEDIATRIC RHABDOMYOSARCOMA

      Oncogene
    38. PAULUSMA CC; KOOL M; BOSMA PJ; SCHEFFER GL; TERBORG F; SCHEPER RJ; TYTGAT GNJ; BORST P; BAAS F; ELFERINK PJO
      A MUTATION IN THE HUMAN CANALICULAR MULTISPECIFIC ORGANIC ANION TRANSPORTER GENE CAUSES THE DUBIN-JOHNSON SYNDROME

      Hepatology
    39. JOBSIS GJ; WEBER JW; BARTH PG; KEIZERS H; BAAS F; VANSCHOONEVELD MJ; VANHILTEN JJ; TROOST D; GEESINK HH; BOLHUIS PA
      AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA WITH RETINAL DEGENERATION (ADCA-II) - CLINICAL AND NEUROPATHOLOGICAL FINDINGS IN 2 PEDIGREES AND GENETIC-LINKAGE TO 3P12-P21.1

      Journal of Neurology, Neurosurgery and Psychiatry
    40. BIKKER H; BAAS F; DEVIJLDER JJM
      MOLECULAR ANALYSIS OF MUTATED THYROID PEROXIDASE DETECTED IN PATIENTSWITH TOTAL IODIDE ORGANIFICATION DEFECTS

      The Journal of clinical endocrinology and metabolism
    41. PIOSIK PA; VANGROENIGEN M; VANDOORN J; BAAS F; DEVIJLDER JJM
      EFFECTS OF MATERNAL THYROID STATUS ON THYROID-HORMONES AND GROWTH IN CONGENITALLY HYPOTHYROID GOAT FETUSES DURING THE 2ND-HALF OF GESTATION

      Endocrinology
    42. KOOL M; DEHAAS M; SCHEFFER GL; SCHEPER RJ; VANEIJK MJT; JUIJN JA; BAAS F; BORST P
      ANALYSIS OF EXPRESSION OF CMOAT (MRP2), MRP3, MRP4, AND MRP5, HOMOLOGS OF THE MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN GENE (MRP1), IN HUMANCANCER CELL-LINES

      Cancer research
    43. ISRAEL FP; WHITE GJ; BAAS F
      CO AND C-I-MAPS OF THE STARBURST GALAXY NGC-253 (VOL 302, PG 343, 1995)

      Astronomy and astrophysics
    44. PREISINGER EA; HIGGINS MJ; MORGENBESSER SD; BAAS F; DASGUPTA S; LANDERS JE; SHOWS TB; HOUSMAN DE
      LOSS OF REPLICATIVE ASYNCHRONY AT THE IMPRINTED REGION ON 11P15.5 IN EMBRYONAL RHABDOMYOSARCOMA

      American journal of human genetics
    45. VALENTIJN LJ; VISSER M; SIJMONS CC; ARCECI RJ; BAAS F
      RNA EDITING IN H19

      American journal of human genetics
    46. JOBSIS GJ; KEIZERS H; VREIJLING JP; DEVISSER M; SPEER MC; WOLTERMAN RA; BAAS F; BOLHUIS PA
      TYPE-VI COLLAGEN MUTATIONS IN BETHLEM MYOPATHY, AN AUTOSOMAL-DOMINANTMYOPATHY WITH CONTRACTURES

      Nature genetics
    47. MEIJERINK PHS; HOOGENDIJK JE; GABREELSFESTEN AAWM; ZORN I; VELDMAN H; BAAS F; DEVISSER M; BOLHUIS PA
      CLINICALLY DISTINCT CODON-69 MUTATIONS IN MAJOR MYELIN PROTEIN ZERO IN DEMYELINATING NEUROPATHIES

      Annals of neurology
    48. PIOSIK PA; VANGROENIGEN M; BAAS F
      EFFECT OF THYROID-HORMONE DEFICIENCY ON RC3 NEUROGRANIN MESSENGER-RNAEXPRESSION IN THE PRENATAL AND ADULT CAPRINE BRAIN/

      Molecular brain research
    49. PIOSIK PA; VANGROENIGEN M; PONNE NJ; VALENTIJN LJ; BOLHUIS PA; BAAS F
      CAPRINE HOMOLOG OF RODENT 5'-AMP-ACTIVATED PROTEIN-KINASE SUBUNIT ANDYEAST SNF4 CAT3 IS DOWN-REGULATED BY THYROID-HORMONE/

      Molecular brain research
    50. EGGSTEIN S; MANTHEY G; HIRSCH T; BAAS F; SPECHT BUV; FARTHMANN EH
      RAF-1 KINASE, EPIDERMAL GROWTH-FACTOR RECEPTORS, AND MUTANT RAS PROTEINS IN COLONIC CARCINOMAS

      Digestive diseases and sciences
    51. JOBSIS GJ; BOLHUIS PA; BOERS JM; BAAS F; WOLTERMAN RA; HENSELS GW; DEVISSER M
      GENETIC LOCALIZATION OF BETHLEM MYOPATHY

      Neurology
    52. VISSER M; BRAS J; SIJMONS C; DEVILEE P; WIJNAENDTS LCD; VANDERLINDEN JC; VOUTE PA; BAAS F
      MICROSATELLITE INSTABILITY IN CHILDHOOD RHABDOMYOSARCOMA IS LOCUS-SPECIFIC AND CORRELATES WITH FRACTIONAL ALLELIC LOSS

      Proceedings of the National Academy of Sciences of the United Statesof America
    53. JUSTTANONT K; SKINNER CJ; TIELENS AGGM; MEIXNER M; BAAS F
      MODELING OF THE DUST AND GAS OUTFLOWS FROM OH-26.5- THE SUPERWIND(0.6)

      The Astrophysical journal
    54. GROENEWEGEN MAT; BAAS F; DEJONG T; LOUP C
      CO AND HCN OBSERVATIONS OF CARBON STARS

      Astronomy and astrophysics
    55. BIKKER H; VULSMA T; BAAS F; DEVIJLDER JJM
      IDENTIFICATION OF 5 NOVEL INACTIVATING MUTATIONS IN THE HUMAN THYROIDPEROXIDASE GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS

      Human mutation
    56. VALENTIJN LJ; OUVRIER RA; VANDENBOSCH NHA; BOLHUIS PA; BAAS F; NICHOLSON GA
      DEJERINE-SOTTAS NEUROPATHY IS ASSOCIATED WITH A DE-NOVO PMP22 MUTATION

      Human mutation
    57. FLORIJN RJ; BONDEN LAJ; VROLIJK H; WIEGANT J; VAANDRAGER JW; BAAS F; DENDUNNEN JT; TANKE HJ; VANOMMEN GJB; RAAP AK
      HIGH-RESOLUTION DNA FIBER-FISH FOR GENOMIC DNA MAPPING AND COLOR BAR-CODING OF LARGE GENES

      Human molecular genetics
    58. PIOSIK PA; VANGROENIGEN M; PONNE NJ; BOLHUIS PA; BAAS F
      RC3 NEUROGRANIN STRUCTURE AND EXPRESSION IN THE CAPRINE BRAIN IN RELATION TO CONGENITAL HYPOTHYROIDISM

      Molecular brain research
    59. JOBSIS GJ; BARTH PG; BOERS JM; BAAS F; BOLHUIS PA; DEVISSER M
      BETHLEM MYOPATHY - CLINICAL AND GENETIC-ASPECTS

      Neurology
    60. ZAMAN GJR; LANKELMA J; VANTELLINGEN O; BEIJNEN J; DEKKER H; PAULUSMA C; OUDEELFERINK RPJ; BAAS F; BORST P
      ROLE OF GLUTATHIONE IN THE EXPORT OF COMPOUNDS FROM CELLS BY THE MULTIDRUG-RESISTANCE-ASSOCIATED PROTEIN

      Proceedings of the National Academy of Sciences of the United Statesof America
    61. JOBSIS GJ; LOUWERSE ES; DEVISSER M; WOLTERMAN RA; BOLHUIS PA; BUSCH HFM; BRUGGENWIRTH HT; BAAS F; WIERSINGA WM; KOELMAN JHTM; DEJONG JMBV
      DIFFERENTIAL-DIAGNOSIS IN SPINAL AND BULBAR MUSCULAR-ATROPHY CLINICALAND MOLECULAR ASPECTS

      Journal of the neurological sciences
    62. EIJDEMS EWHM; DEHAAS M; COCOMARTIN JM; OTTENHEIM CPE; ZAMAN GJR; DAUWERSE HG; BREUNING MH; TWENTYMAN PR; BORST P; BAAS F
      MECHANISMS OF MRP OVER-EXPRESSION IN 4 HUMAN LUNG-CANCER CELL-LINES AND ANALYSIS OF THE MRP AMPLICON

      International journal of cancer
    63. EIJDEMS EWHM; ZAMAN GJR; DEHAAS M; VERSANTVOORT CHM; FLENS MJ; SCHEPER RJ; KAMST E; BORST P; BAAS F
      ALTERED MRP IS ASSOCIATED WITH MULTIDRUG-RESISTANCE AND REDUCED DRUG ACCUMULATION IN HUMAN SW-1573 CELLS

      British Journal of Cancer
    64. EIJDEMS EWHM; DEHAAS M; TIMMERMAN AJ; VANDERSCHANS GP; KAMST E; DENOOIJ J; RICOTTI GCBA; BORST P; BAAS F
      REDUCED TOPOISOMERASE-II ACTIVITY IN MULTIDRUG-RESISTANT HUMAN NONSMALL CELL LUNG-CANCER CELL-LINES

      British Journal of Cancer
    65. ISRAEL FP; WHITE GJ; BAAS F
      CO AND C-I MAPS OF THE STARBURST GALAXY NGC-253

      Astronomy and astrophysics
    66. WATERS LBFM; VANDENANCKER ME; BAAS F; VANDERBLIEK NS; BONTEKOE TR; GEBALLE TR; GRADY CA; KESTER DJM; OUDMAIJER RD; SANDELL G; THE PS; VEGA R; VANWINCKEL H
      CIRCUMSTELLAR GAS AND DUST IN 68-OPHIUCHI (A0-IVE)

      Astronomy and astrophysics
    67. ISRAEL FP; TACCONI LJ; BAAS F
      CO OBSERVATIONS OF 25 DWARF GALAXIES

      Astronomy and astrophysics
    68. MARIMAN ECM; GABREELSFESTEN AAWM; VANBEERSUM SEC; VALENTIJN LJ; BOLHUIS PA; BAAS F; ROPERS HH; GABREELS FJM
      ELUCIDATION OF THE MOLECULAR DEFECT CAUSING A SEVERE TYPE OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES COMMON 1.5 MB DELETION IN CHROMOSOME-17P

      American journal of human genetics
    69. BAAS F; MEIJERINK PHS; ZORN I; BOLHUIS PA
      EXON TRAPPING IDENTIFIES A NOVEL PROTEIN KINASE-LIKE GENE WITHIN THE 64 KB INTRON OF THE HUMAN THYROGLOBULIN GENE

      American journal of human genetics
    70. MEIJERINK PHS; ZORN I; KENNERSON ML; ROSS DA; NICHOLSON GA; BOLHUIS PA; BAAS F
      NOVEL GENES IN THE CMT1A-ASSOCIATED DNA DUPLICATION ON CHROMOSOME 17P11.2 IDENTIFIED BY EXON AMPLIFICATION

      American journal of human genetics
    71. NICHOLSON GA; VALENTIJN LJ; CHERRYSON AK; KENNERSON ML; BRAGG TL; DEKROON RM; ROSS DA; POLLARD JD; MCLEOD JG; BOLHUIS PA; BAAS F
      A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (VOL 6, PG 263, 1994)

      Nature genetics
    72. NICHOLSON GA; VALENTIJN LJ; CHERRYSON AK; KENNERSON ML; BRAGG TL; DEKROON RM; ROSS DA; POLLARD JD; MCLEOD JG; BOLHUIS PA; BAAS F
      A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Nature genetics
    73. JANSSEN EAM; HENSELS GW; VANOOST BA; HAMEL BCJ; KEMP S; BAAS F; WEBER JW; BARTH PG; BOLHUIS PA
      THE GENE FOR X-LINKED MYOTUBULAR MYOPATHY IS LOCATED IN AN 8-MB REGION AT THE BORDER OF XQ27.3 AND XQ28

      Neuromuscular disorders
    74. BORST P; SCHINKEL AH; BAAS F; SMIT JJM; EIJDEMS LWHM; ZAMAN GJR; SMITH SJ
      MECHANISMS OF MULTIDRUG-RESISTANCE

      Journal of cellular biochemistry
    75. HU JY; HEKKERT PTL; SLIJKHUIS S; BAAS F; SAHAI R; WOOD PR
      A SYSTEMATIC STUDY OF IRAS SELECTED PROTOPLANETARY NEBULA CANDIDATES .2. OH AND CO OBSERVATIONS

      Astronomy & Astrophysics. Supplement series
    76. MARIMAN ECM; GABREELSFESTEN AAWM; VANBEERSUM SEC; VALENTIJN LJ; BAAS F; BOLHUIS PA; JONGEN PJH; ROPERS HH; GABREELS FJM
      PREVALENCE OF THE 1.5-MB 17P DELETION IN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Annals of neurology
    77. MARIMAN ECM; GABREELSFESTEN AAWM; VANBEERSUM SEC; JONGEN PJH; VANDELOOIJ E; BAAS F; BOLHUIS PA; ROPERS HH; GABREELS FJM
      EVIDENCE FOR GENETIC-HETEROGENEITY UNDERLYING HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Human genetics
    78. ZAMAN GJR; FLENS MJ; VANLEUSDEN MR; DEHAAS M; MULDER HS; LANKELMA J; PINEDO HM; SCHEPER RJ; BAAS F; BROXTERMAN HJ; BORST P
      THE HUMAN MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN MRP IS A PLASMA-MEMBRANE DRUG-EFFLUX PUMP

      Proceedings of the National Academy of Sciences of the United Statesof America
    79. BIKKER H; DENHARTOG MT; BAAS F; GONS MH; VULSMA T; DEVIJLDER JJM
      A 20-BASEPAIR DUPLICATION IN THE HUMAN THYROID PEROXIDASE GENE RESULTS IN A TOTAL IODIDE ORGANIFICATION DEFECT AND CONGENITAL HYPOTHYROIDISM

      The Journal of clinical endocrinology and metabolism
    80. KASTNER H; WEINTRAUB DA; SNELL RL; SANDELL G; ASPIN C; HUGHES DH; BAAS F
      THE MASSIVE MOLECULAR OUTFLOW FROM CRL-2136-IRS-1

      The Astrophysical journal
    81. BAAS F; ISRAEL FP; KOORNNEEF J
      MOLECULES IN THE STARBURST GALAXY HENIZE-2-10

      Astronomy and astrophysics
    82. KULKENS T; BOLHUIS PA; WOLTERMAN RA; KEMP S; TENIJENHUIS S; VALENTIJN LJ; HENSELS GW; JENNEKENS FGI; DEVISSER M; HOOGENDIJK JE; BAAS F
      DELETION OF THE SERINE-34 CODON FROM THE MAJOR PERIPHERAL MYELIN PROTEIN-P(0) GENE IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1B

      Nature genetics
    83. VALENTIJN LJ; BAAS F; ZORN I; HENSELS GW; DEVISSER M; BOLHUIS PA
      ALTERNATIVELY SIZED DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A

      Human molecular genetics
    84. DAUWERSE JG; WESSELS JW; GILES RH; WIEGANT J; VANDERREIJDEN BA; FUGAZZA G; JUMELET EA; SMIT E; BAAS F; RAAP AK; HAGEMEIJER A; BEVERSTOCK GC; VANOMMEN GJB; BREUNING MH
      CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO

      Human molecular genetics
    85. GROENEWEGEN MAT; DEJONG T; BAAS F
      NEAR-INFRARED AND SUBMILLIMETER PHOTOMETRY OF CARBON STARS

      Astronomy & Astrophysics. Supplement series
    86. BORST P; SCHINKEL AH; SMIT JJM; WAGENAAR E; VANDEEMTER L; SMITH AJ; EIJDEMS EWHM; BAAS F; ZAMAN GJR
      CLASSICAL AND NOVEL FORMS OF MULTIDRUG-RESISTANCE AND THE PHYSIOLOGICAL FUNCTIONS OF P-GLYCOPROTEINS IN MAMMALS

      Pharmacology & therapeutics
    87. HOOGENDIJK JE; JANSSEN EAM; GABREELSFESTEN AAWM; HENSELS GW; JOOSTEN EMG; GABREELS FJM; ZORN I; VALENTIJN LJ; BAAS F; DEVISSER BWO; DEVISSER M; BOLHUIS PA
      ALLELIC HETEROGENEITY IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA (CHARCOT-MARIE-TOOTH DISEASE TYPE-1A)

      Neurology
    88. SCHINKEL AH; ARCECI RJ; SMIT JJM; WAGENAAR E; BAAS F; DOLLE M; TSURUO T; MECHETNER EB; RONINSON IB; BORST P
      BINDING-PROPERTIES OF MONOCLONAL-ANTIBODIES RECOGNIZING EXTERNAL EPITOPES OF THE HUMAN MDR1 P-GLYCOPROTEIN

      International journal of cancer
    89. HENSELS GW; JANSSEN EAM; HOOGENDIJK JE; VALENTIJN LJ; BAAS F; BOLHUIS PA
      QUANTITATIVE MEASUREMENT OF DUPLICATED DNA AS A DIAGNOSTIC-TEST FOR CHARCOT-MARIE-TOOTH DISEASE TYPE-1A

      Clinical chemistry
    90. ZAMAN GJR; VERSANTVOORT CHM; SMIT JJM; EIJDEMS EWHM; DEHAAS M; SMITH AJ; BROXTERMAN HJ; MULDER NH; DEVRIES EGE; BAAS F; BORST P
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      Cancer research
    91. BOLHUIS PA; PONNE NJ; BIKKER H; BAAS F; DEJONG JMBV
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      Biochimica et biophysica acta
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      The Astrophysical journal
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      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 20:09:42