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    1. Arteaga, HJ; Mohamed, AJ; Christensson, B; Gahrton, G; Smith, CIE; Dilber, MS
      Expression and release of stable and active forms of murine granulocyte-macrphage colony-stimulating factor (mGM-CSF) targeted to different subcellular compartments

      CYTOKINE
    2. Aints, A; Guven, H; Gahrton, G; Smith, CIE; Dilber, MS
      Mapping of herpes simplex virus-1 VP22 functional domains for inter- and subcellular protein targeting

      GENE THERAPY
    3. Branden, LJ; Christensson, B; Smith, CIE
      In vivo nuclear delivery of oligonucleotides via hybridizing bifunctional peptides

      GENE THERAPY
    4. Volpe, CP; Lundgren, A; Aints, A; Mohamed, AJ; Jaakkola, P; Christensson, B; Gahrton, G; Jalkanen, M; Smith, CIE; Dilber, MS
      Proximal promoter of the murine syndecan-1 gene is not sufficient for the developmental pattern of syndecan expression in B lineage cells

      AMERICAN JOURNAL OF HEMATOLOGY
    5. Smith, CIE; Islam, TC; Mattsson, PT; Mohamed, AJ; Nore, BF; Vihinen, M
      The Tec family of cytoplasmic tyrosine kinases: mammalian Btk, Bmx, Itk, Tec, Txk and homologs in other species

      BIOESSAYS
    6. Verloes, A; Dresse, MF; Keutgen, H; Asplund, C; Smith, CIE
      Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Wang, DM; Boylin, EC; Minegishi, Y; Wen, RR; Smith, CIE; Ihle, JN; Conley, ME
      Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology

      IMMUNOGENETICS
    8. Fieschi, C; Dupuis, S; Picard, C; Smith, CIE; Holland, SM; Casanova, JL
      High levels of interferon gamma in the plasma of children with complete interferon gamma receptor deficiency

      PEDIATRICS
    9. Wood, PMD; Mayne, A; Joyce, H; Smith, CIE; Granoff, DM; Kumararatne, DS
      A mutation in Bruton's tyrosine kinase as a cause of selective anti-polysaccharide antibody deficiency

      JOURNAL OF PEDIATRICS
    10. Hansson, H; Smith, CIE; Hard, T
      Both proline-rich sequences in the TH region of Bruton's tyrosine kinase stabilize intermolecular interactions with the SH3 domain

      FEBS LETTERS
    11. Hansson, H; Okoh, MP; Smith, CIE; Vihinen, M; Hard, T
      Intermolecular interactions between the SH3 domain and the proline-rich THregion of Bruton's tyrosine kinase

      FEBS LETTERS
    12. Islam, TC; Branden, LJ; Kohn, DB; Islam, KB; Smith, CIE
      BTK mediated apoptosis, a possible mechanism for failure to generate high titer retroviral producer clones

      JOURNAL OF GENE MEDICINE
    13. Vihinen, M; Mattsson, PT; Smith, CIE
      Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA)

      FRONTIERS IN BIOSCIENCE
    14. Nera, KP; Brockmann, E; Vihinen, M; Smith, CIE; Mattsson, PT
      Rational design and purification of human Bruton's tyrosine kinase SH3-SH2protein for structure-function studies

      PROTEIN EXPRESSION AND PURIFICATION
    15. Smith, CIE
      Experiments of nature: primary immune defects deciphered and defeated

      IMMUNOLOGICAL REVIEWS
    16. Islam, TC; Smith, CIE
      The cellular phenotype conditions Btk for cell survival or apoptosis signaling

      IMMUNOLOGICAL REVIEWS
    17. Mattsson, PT; Lappalainen, I; Backesjo, CM; Brockmann, E; Lauren, S; Vihinen, M; Smith, CIE
      Six X-linked agammaglobulinemia-causing missense mutations in the src homology 2 domain of Bruton's tyrosine kinase: Phosphotyrosine-binding and circular dichroism analysis

      JOURNAL OF IMMUNOLOGY
    18. Mohamed, AJ; Vargas, L; Nore, BF; Backesjo, CM; Christenssonn, B; Smith, CIE
      Nucleocytoplasmic shuttling of Bruton's tyrosine kinase

      JOURNAL OF BIOLOGICAL CHEMISTRY
    19. Nore, BF; Vargas, L; Mohamed, AJ; Branden, LJ; Backesjo, CM; Islam, TC; Mattsson, PT; Hultenby, K; Christensson, B; Smith, CIE
      Redistribution of Bruton's tyrosine kinase by activation of phosphatidylinositol 3-kinase and Rho-family GTPases

      EUROPEAN JOURNAL OF IMMUNOLOGY
    20. Aints, A; Dilber, MS; Smith, CIE
      Intercellular spread of GFP-VP22

      JOURNAL OF GENE MEDICINE
    21. Branden, LJ; Mohamed, AJ; Smith, CIE
      A peptide nucleic acid-nuclear localization signal fusion that mediates nuclear transport of DNA

      NATURE BIOTECHNOLOGY
    22. Vihinen, M; Kwan, SP; Lester, T; Ochs, HD; Resnick, I; Valiaho, J; Conley, ME; Smith, CIE
      Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia

      HUMAN MUTATION
    23. Mohamed, AJ; Nore, BF; Christensson, B; Smith, CIE
      Signalling of Bruton's tyrosine kinase, Btk

      SCANDINAVIAN JOURNAL OF IMMUNOLOGY
    24. Quartier, P; Debre, M; De Blic, J; de Sauverzac, R; Sayegh, N; Jabado, N; Haddad, E; Blanche, S; Casanova, JL; Smith, CIE; Le Deist, F; de Saint Basille, G; Fischer, A
      Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: A retrospective survey of 31 patients

      JOURNAL OF PEDIATRICS
    25. Muller, S; Maas, A; Islam, TC; Sideras, P; Suske, G; Philipsen, S; Xanthopoulos, KG; Hendriks, RW; Smith, CIE
      Synergistic activation of the human Btk promoter by transcription factors Sp1/3 and PU.1

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    26. KNAPP S; MATTSON PT; CHRISTOVA P; BERNDT KD; KARSHIKOFF A; VIHINEN M; SMITH CIE; LADENSTEIN R
      THERMAL UNFOLDING OF SMALL PROTEINS WITH SH3 DOMAIN FOLDING PATTERN

      Proteins
    27. SMITH CIE; BACKESJO CM; BERGLOF A; BRANDEN LJ; ISLAM T; MATTSSON PT; MOHAMED AJ; MULLER S; NORE B; VIHINEN M
      X-LINKED AGAMMAGLOBULINEMIA - LACK OF MATURE B-LINEAGE CELLS CAUSED BY MUTATIONS IN THE BTK KINASE

      Perspectives in mathematical logic
    28. VIHINEN M; BRANDAU O; BRANDEN LJ; KWAN SP; LAPPALAINEN I; LESTER T; NOORDZIJ JG; OCHS HD; OLLILA J; PIENAAR SM; RIIKONEN P; SAHA BK; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    29. HOLINSKIFEDER E; WEISS M; BRANDAU O; JEDELE KB; NORE B; BACKESJO CM; VIHINEN M; HUBBARD SR; BELOHRADSKY BH; SMITH CIE; MEINDL A
      MUTATION SCREENING OF THE BTK GENE IN 56 FAMILIES WITH X-LINKED AGAMMAGLOBULINEMIA (XLA) - 47 UNIQUE MUTATIONS WITHOUT CORRELATION TO CLINICAL COURSE

      Pediatrics
    30. BASKIN B; ISLAM KB; SMITH CIE
      CHARACTERIZATION OF THE CDR3 REGION OF REARRANGED ALPHA-HEAVY-CHAIN GENES IN HUMAN FETAL LIVER

      Clinical and experimental immunology
    31. HANSSON H; MATTSSON PT; ALLARD P; HAAPANIEMI P; VIHINEN M; SMITH CIE; HARD T
      SOLUTION STRUCTURE OF THE SH3 DOMAIN FROM BRUTONS TYROSINE KINASE

      Biochemistry
    32. VIHINEN M; SMITH CIE
      INTERACTIONS BETWEEN SH2 AND SH3 DOMAINS

      Biochemical and biophysical research communications
    33. VORECHOVSKY I; LUO LP; HERTZ JM; FROLAND SS; KLEMOLA T; FIORINI M; QUINTI I; PAGANELLI R; OZSAHIN H; HAMMARSTROM L; WEBSTER ADB; SMITH CIE
      MUTATION PATTERN IN BRUTON TYROSINE KINASE GENE IN 26 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

      Human mutation
    34. LAPPALAINEN I; OLLILA J; SMITH CIE; VIHINEN M
      REGISTRIES OF IMMUNODEFICIENCY PATIENTS AND MUTATIONS

      Human mutation
    35. BJORKSTRAND B; SMITH CIE; SUNDBERG M; SUNDMANENGBERG B; DILBER MS; LJUNGMAN P; GAHRTON G
      AUTOLOGOUS STEM-CELL TRANSPLANTATION WITH GENE MARKED CELLS IN MULTIPLE-MYELOMA

      Cancer gene therapy
    36. ISLAM KB; BLOMBERG P; WIKSTROM K; SMITH CIE
      AN ACADEMIC CENTER FOR GENE-THERAPY RESEARCH WITH CLINICAL GRADE MANUFACTURING CAPABILITY

      Annals of medicine
    37. VIHINEN M; BELOHRADSKY BH; HAIRE RN; HOLINSKIFEDER E; KWAN SP; LAPPALAINEN I; LEHVASLAIHO H; LESTER T; MEINDL A; OCHS H; OLLILA J; VORECHOVSKY I; WEISS M; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (VOL 25, PG 166, 1997)

      Nucleic acids research
    38. VIHINEN M; BELOHRADSKY BH; HAIRE RN; HOLINSKIFEDER E; KWAN SP; LAPPALAINEN I; LEHVASLAIHO H; LESTER T; MEINDL A; OCHS HD; OLLILA J; VORECHOVSKY I; WEISS M; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    39. VIHINEN M; NORE BF; MATTSSON PT; BACKESJO CM; NARS M; KOUTANIEMI S; WATANABE C; LESTER T; JONES A; OCHS HD; SMITH CIE
      MISSENSE MUTATIONS AFFECTING A CONSERVED CYSTEINE PAIR IN THE TH DOMAIN OF BTK

      FEBS letters
    40. BERGLOF A; SANDSTEDT K; FEINSTEIN R; BOLSKE G; SMITH CIE
      B-CELL-DEFICIENT MU-MT MICE AS AN EXPERIMENTAL-MODEL FOR MYCOPLASMA-INFECTIONS IN X-LINKED AGAMMAGLOBULINEMIA

      European Journal of Immunology
    41. BASKIN B; ISLAM KB; EVENGARD B; EMTESTAM L; SMITH CIE
      DIRECT AND SEQUENTIAL SWITCHING FROM MU TO EPSILON IN PATIENTS WITH SCHISTOSOMA-MANSONI INFECTION AND ATOPIC-DERMATITIS

      European Journal of Immunology
    42. SANDSTEDT K; BERGLOF A; FEINSTEIN R; BOLSKE G; EVENGARD B; SMITH CIE
      DIFFERENTIAL SUSCEPTIBILITY TO MYCOPLASMA-PULMONIS INTRANASAL INFECTION IN X-LINKED IMMUNODEFICIENT (XID), SEVERE COMBINED IMMUNODEFICIENT (SCID), AND IMMUNOCOMPETENT MICE

      Clinical and experimental immunology
    43. DILBER MS; ABEDI MR; CHRISTENSSON B; BJORKSTRAND B; KIDDER GM; NAUS CCG; GAHRTON G; SMITH CIE
      GAP-JUNCTIONS PROMOTE THE BYSTANDER EFFECT OF HERPES-SIMPLEX VIRUS THYMIDINE KINASE IN-VIVO

      Cancer research
    44. BRANDEN L; SMITH CIE; GAHRTON G
      REVERSE FLOW-THROUGH TRANSDUCTION - A NEW METHOD FOR GENE DELIVERY

      Blood
    45. PETTERSSON E; BASKIN B; REKOLA S; ISLAM KB; SMITH CIE
      MOLECULAR-BASIS OF IGA IN IGA NEPHROPATHY

      Journal of the American Society of Nephrology
    46. VIHINEN M; SMITH CIE
      STRUCTURAL ASPECTS OF SIGNAL-TRANSDUCTION IN B-CELLS

      Critical reviews in immunology
    47. SANDERS R; BINISLAM K; BETZ R; LARSSON C; SMITH CIE
      A HUMAN HOMOLOG OF THE RAT RAB GERANYLGERANYL TRANSFERASE BETA-SUBUNIT ON CHROMOSOME 1P22-P-31

      Genomics
    48. VIHINEN M; IWATA T; KINNON C; KWAN SP; OCHS HD; VORECHOVSKY I; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    49. MATTSSON PT; VIHINEN M; SMITH CIE
      X-LINKED AGAMMAGLOBULINEMIA (XLA) - A GENETIC TYROSINE KINASE (BTK) DISEASE

      BioEssays
    50. SALIM K; BOTTOMLEY MJ; QUERFURTH E; ZVELEBIL MJ; GOUT I; SCAIFE R; MARGOLIS RL; GIGG R; SMITH CIE; DRISCOLL PC; WATERFIELD MD; PANAYOTOU G
      DISTINCT SPECIFICITY IN THE RECOGNITION OF PHOSPHOINOSITIDES BY THE PLECKSTRIN HOMOLOGY DOMAINS OF DYNAMIN AND BRUTONS TYROSINE KINASE

      EMBO journal
    51. SMITH CIE; VIHINEN M
      IMMUNODEFICIENCY MUTATION DATABASES - A NEW RESEARCH TOOL

      Immunology today
    52. RABBANI H; PAN Q; KONDO N; SMITH CIE; HAMMARSTROM L
      DUPLICATIONS AND DELETIONS OF THE HUMAN IGHC LOCUS - EVOLUTIONARY IMPLICATIONS

      Immunogenetics
    53. OCHS HD; SMITH CIE
      X-LINKED AGAMMAGLOBULINEMIA - A CLINICAL AND MOLECULAR ANALYSIS

      Medicine
    54. LEUSEN JHW; DEKLEIN A; HILARIUS PM; AHLIN A; PALMBLAD J; SMITH CIE; DIEKMANN D; HALL A; VERHOEVEN AJ; ROOS D
      DISTURBED INTERACTION OF P21-RAC WITH MUTATED P67-PHOX CAUSES CHRONICGRANULOMATOUS-DISEASE

      The Journal of experimental medicine
    55. BASKIN B; PETTERSSON E; REKOLA S; SMITH CIE; ISLAM KB
      STUDIES OF THE MOLECULAR-BASIS OF IGA PRODUCTION, SUBCLASS REGULATIONAND CLASS-SWITCH RECOMBINATION IN IGA NEPHROPATHY PATIENTS

      Clinical and experimental immunology
    56. ABEDI MR; HAMMARSTROM L; BROOME U; ANGELIN B; SMITH CIE; CHRISTENSSON B
      REDUCTION IN SERUM LEVELS OF ANTIMITOCHONDRIAL (M2) ANTIBODIES FOLLOWING IMMUNOGLOBULIN THERAPY IN SEVERE COMBINED IMMUNODEFICIENT (SCID) MICE RECONSTITUTED WITH LYMPHOCYTES FROM PATIENTS WITH PRIMARY BILIARY-CIRRHOSIS (PBC)

      Clinical and experimental immunology
    57. DILBER MS; ABEDI MR; BJORKSTRAND B; CHRISTENSSON B; GAHRTON G; XANTHOPOULOS KG; SMITH CIE
      SUICIDE GENE-THERAPY FOR PLASMA-CELL TUMORS

      Blood
    58. JIN H; WEBSTER ADB; VIHINEN M; SIDERAS P; VORECHOVSKY I; HAMMARSTROM L; BERNATOWSKAMATUSZKIEWICZ E; SMITH CIE; BOBROW M; VETRIE D
      IDENTIFICATION OF BTK MUTATIONS IN 20 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Human molecular genetics
    59. VORECHOVSKY I; LUO LP; DESAINTBASILE G; HAMMARSTROM L; WEBSTER ADB; SMITH CIE
      IMPROVED OLIGONUCLEOTIDE PRIMER SET FOR MOLECULAR DIAGNOSIS OF X-LINKED AGAMMAGLOBULINEMIA - PREDOMINANCE OF AMINO-ACID SUBSTITUTIONS IN THE CATALYTIC DOMAIN OF BRUTONS TYROSINE KINASE

      Human molecular genetics
    60. VORECHOVSKY I; VIHINEN M; DESAINTBASILE G; HONSOVA S; HAMMARSTROM L; MULLER S; NILSSON L; FISCHER A; SMITH CIE
      DNA-BASED MUTATION ANALYSIS OF BRUTONS TYROSINE KINASE GENE IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

      Human molecular genetics
    61. TRUEDSSON L; BASKIN B; PAN Q; RABBANI H; VORECHOVSKY I; SMITH CIE; HAMMARSTROM L
      GENETICS OF IGA DEFICIENCY

      APMIS. Acta pathologica, microbiologica et immunologica Scandinavica
    62. LI KJ; DILBER MS; ABEDI MR; BJORKSTRAND B; SMITH CIE; GAROFF H; GAHRTON G; XANTHOPOULOS KG
      RETROVIRAL-MEDIATED GENE-TRANSFER INTO HUMAN BONE-MARROW STROMAL CELLS - STUDIES OF EFFICIENCY AND IN-VIVO SURVIVAL IN SCID MICE

      European journal of haematology
    63. AHLIN A; DEBOER M; ROOS D; LEUSEN J; SMITH CIE; SUNDIN U; RABBANI H; PALMBLAD J; ELINDER G
      PREVALENCE, GENETICS AND CLINICAL PRESENTATION OF CHRONIC GRANULOMATOUS-DISEASE IN SWEDEN

      Acta paediatrica
    64. SMITH CIE; HAMMARSTROM L
      POSITIONAL CLONING ACID THE MOLECULAR-BASIS OF IMMUNODEFICIENCY

      Annals of medicine
    65. SMITH CIE; BRANDEN LJ; KOHN DB; XANTHOPOULOS KG
      RETROVIRAL GENE-TRANSFER TO XID BONE-MARROW CELLS - AN EXPERIMENTAL-MODEL FOR GENE-THERAPY IN X-LINKED AGAMMAGLOBULINEMIA

      Journal of cellular biochemistry
    66. GARDULF A; BJORVELL H; ANDERSEN V; BJORKANDER J; ERICSON D; FROLAND SS; GUSTAFSON R; HAMMARSTROM L; NYSTROM T; SOEBERG B; SMITH CIE
      LIFELONG TREATMENT WITH GAMMA-GLOBULIN FOR PRIMARY ANTIBODY DEFICIENCIES - THE PATIENTS EXPERIENCES OF SUBCUTANEOUS SELF-INFUSIONS AND HOMETHERAPY

      Journal of advanced nursing
    67. VIHINEN M; COOPER MD; DESAINTBASILE G; FISCHER A; GOOD RA; HENDRIKS RW; KINNON C; KWAN SP; LITMAN GW; NOTARANGELO LD; OCHS HD; ROSEN FS; VETRIE D; WEBSTER ADB; ZEGERS BJM; SMITH CIE
      BTKBASE - A DATABASE OF XLA-CAUSING MUTATIONS

      Immunology today
    68. GARDULF A; ANDERSEN V; BJORKANDER J; ERICSON D; FROLAND SS; GUSTAFSON R; HAMMARSTROM L; JACOBSEN MB; JONSSON E; MOLLER G; NYSTROM T; SOEBERG B; SMITH CIE
      SUBCUTANEOUS IMMUNOGLOBULIN REPLACEMENT IN PATIENTS WITH PRIMARY ANTIBODY DEFICIENCIES - SAFETY AND COSTS

      Lancet
    69. VORECHOVSKY I; KOSKINEN S; PAGANELLI R; SMITH CIE; BUSSLINGER M; HAMMARSTROM L
      THE PAX5 GENE - A LINKAGE AND MUTATION ANALYSIS IN CANDIDATE HUMAN PRIMARY IMMUNODEFICIENCIES

      Immunogenetics
    70. VORECHOVSKY I; ZETTERQUIST H; PAGANELLI R; KOSKINEN S; WEBSTER ADB; BJORKANDER J; SMITH CIE; HAMMARSTROM L
      FAMILY AND LINKAGE STUDY OF SELECTIVE IGA DEFICIENCY AND COMMON VARIABLE IMMUNODEFICIENCY

      Clinical immunology and immunopathology
    71. MANIAR HS; VIHINEN M; WEBSTER ADB; NILSSON L; SMITH CIE
      STRUCTURAL BASIS FOR X-LINKED AGAMMAGLOBULINEMIA (XLA) - MUTATIONS ATINTERACTING BTK RESIDUES R562, W563, AND A582

      Clinical immunology and immunopathology
    72. RABBANI H; KONDO N; SMITH CIE; HAMMARSTROM L
      THE INFLUENCE OF GENE DELETIONS AND DUPLICATIONS WITHIN THE IGHC LOCUS ON SERUM IMMUNOGLOBULIN SUBCLASS LEVELS

      Clinical immunology and immunopathology
    73. SAMUELSON A; BORRELLI S; GUSTAFSON R; HAMMARSTROM L; SMITH CIE; JONASSON J; LINDBERG AA
      CHARACTERIZATION OF HAEMOPHILUS-INFLUENZAE ISOLATES FROM THE RESPIRATORY-TRACT OF PATIENTS WITH PRIMARY ANTIBODY DEFICIENCIES - EVIDENCE FOR PERSISTENT COLONIZATIONS

      Scandinavian journal of infectious diseases
    74. ISLAM KB; RABBANI H; LARSSON C; SANDERS R; SMITH CIE
      MOLECULAR-CLONING, CHARACTERIZATION, AND CHROMOSOMAL LOCALIZATION OF A HUMAN LYMPHOID TYROSINE KINASE RELATED TO MURINE BLK

      The Journal of immunology
    75. VIHINEN M; ZVELEBIL MJJM; ZHU QL; BROOIMANS RA; OCHS HD; ZEGERS BJM; NILSSON L; WATERFIELD MD; SMITH CIE
      STRUCTURAL BASIS FOR PLECKSTRIN HOMOLOGY DOMAIN MUTATIONS IN X-LINKEDAGAMMAGLOBULINEMIA

      Biochemistry
    76. BJORKSTRAND B; GAHRTON G; DILBER MS; LJUNGMAN P; SMITH CIE; XANTHOPOULOS KG
      RETROVIRAL-MEDIATED GENE-TRANSFER OF CD34-ENRICHED BONE-MARROW AND PERIPHERAL-BLOOD CELLS DURING AUTOLOGOUS STEM-CELL TRANSPLANTATION FOR MULTIPLE-MYELOMA

      Human gene therapy
    77. VORECHOVSKY I; KURZBAUER R; KOZMIK Z; HAMMARSTROM L; SMITH CIE; BUSSLINGER M
      SSCP SACI POLYMORPHISM IN THE PAX5 GENE

      Human molecular genetics
    78. VORECHOVSKY I; KOZMIK Z; HAMMARSTROM L; SMITH CIE; BUSSLINGER M
      AN INTRAGENIC TAQI RFLP AT THE PAX5 LOCUS

      Human molecular genetics
    79. TAMAGNONE L; LAHTINEN I; MUSTONEN T; VIRTANEVA K; FRANCIS F; MUSCATELLI F; ALITALO R; SMITH CIE; LARSSON C; ALITALO K
      BMX, A NOVEL NONRECEPTOR TYROSINE KINASE GENE OF THE BTK ITK/TEC/TXK FAMILY LOCATED IN CHROMOSOME XP22.2/

      Oncogene
    80. VORECHOVSKY I; VETRIE D; HOLLAND J; BENTLEY DR; THOMAS K; ZHOU JN; NOTARANGELO LD; PLEBANI A; FONTAN G; OCHS HD; HAMMARSTROM L; SIDERAS P; SMITH CIE
      ISOLATION OF COSMID AND CDNA CLONES IN THE REGION SURROUNDING THE BTKGENE AT XQ21.3-Q22

      Genomics
    81. SMITH CIE; VORECHOVSKY I; SIDERAS P; BASKIN B; HAMMARSTROM L; BRANDEN L; MULLER S; XANTHOPOULOS KG; VETRIE D
      X-LINKED AGAMMAGLOBULINEMIA (XLA), A CANDIDATE DISEASE FOR GENE-THERAPY

      Journal of cellular biochemistry
    82. DILBER MS; BJORKSTRAND B; LI KJ; SMITH CIE; XANTHOPOULOS KG; GAHRTON G
      BASIC FIBROBLAST GROWTH-FACTOR INCREASES RETROVIRAL-MEDIATED GENE-TRANSFER INTO HUMAN HEMATOPOIETIC PERIPHERAL-BLOOD PROGENITOR CELLS

      Experimental hematology
    83. NORHAGEN G; ENGSTROM PE; BJORKSTRAND B; HAMMARSTROM L; SMITH CIE; RINGDEN O
      SALIVARY AND SERUM IMMUNOGLOBULINS IN RECIPIENTS OF TRANSPLANTED ALLOGENEIC AND AUTOLOGOUS BONE-MARROW

      Bone marrow transplantation
    84. YAP PL; MCOMISH F; WEBSTER ADB; HAMMARSTROM L; SMITH CIE; BJORKANDER J; OCHS HD; FISCHER SH; QUINTI I; SIMMONDS P
      HEPATITIS-C VIRUS TRANSMISSION BY INTRAVENOUS IMMUNOGLOBULIN

      Journal of hepatology
    85. HAMMARSTROM L; GARDULF A; HAMMARSTROM V; JANSON A; SMITH CIE; LINDBERG K
      SYSTEMIC AND TOPICAL IMMUNOGLOBULIN TREATMENT IN IMMUNOCOMPROMISED PATIENTS

      Immunological reviews
    86. SMITH CIE; ISLAM KB; VORECHOVSKY I; OLERUP O; WALLIN E; RABBANI H; BASKIN B; HAMMARSTROM L
      X-LINKED AGAMMAGLOBULINEMIA AND OTHER IMMUNOGLOBULIN DEFICIENCIES

      Immunological reviews
    87. VIHINEN M; VETRIE D; MANIAR HS; OCHS HD; ZHU QL; VORECHOVSKY I; WEBSTER ADB; NOTARANGELO LD; NILSSON L; SOWADSKI JM; SMITH CIE
      STRUCTURAL BASIS FOR CHROMOSOME X-LINKED AGAMMAGLOBULINEMIA - A TYROSINE KINASE DISEASE

      Proceedings of the National Academy of Sciences of the United Statesof America
    88. SIDERAS P; MULLER S; SHIELS H; JIN H; KHAN WN; NILSSON L; PARKINSON E; THOMAS JD; BRANDEN L; LARSSON I; PAUL WE; ROSEN FS; ALT FW; VETRIE D; SMITH CIE; XANTHOPOULOS KG
      GENOMIC ORGANIZATION OF MOUSE AND HUMAN BRUTONS AGAMMAGLOBULINEMIA TYROSINE KINASE (BTK) LOCI

      The Journal of immunology
    89. ISLAM KB; BASKIN B; NILSSON L; HAMMARSTROM L; SIDERAS P; SMITH CIE
      MOLECULAR ANALYSIS OF IGA DEFICIENCY - EVIDENCE FOR IMPAIRED SWITCHING TO IGA

      The Journal of immunology
    90. SMITH CIE; BASKIN B; HUMIREGREIFF P; ZHOU JN; OLSSON PG; MANIAR HS; KJELLEN P; LAMBRIS JD; CHRISTENSSON B; HAMMARSTROM L; BENTLEY D; VETRIE D; ISLAM KB; VORECHOVSKY I; SIDERAS P
      EXPRESSION OF BRUTONS AGAMMAGLOBULINEMIA TYROSINE KINASE GENE, BTK, IS SELECTIVELY DOWN-REGULATED IN T-LYMPHOCYTES AND PLASMA-CELLS

      The Journal of immunology
    91. ZHU QL; ZHANG M; RAWLINGS DJ; VIHINEN M; HAGEMANN T; SAFFRAN DC; KWAN SP; NILSSON L; SMITH CIE; WITTE ON; CHEN SH; OCHS HD
      DELETION WITHIN THE SRC HOMOLOGY DOMAIN-3 OF BRUTON TYROSINE KINASE RESULTING IN X-LINKED AGAMMAGLOBULINEMIA (XLA)

      The Journal of experimental medicine
    92. VIHINEN M; NILSSON L; SMITH CIE
      TEC HOMOLOGY (TH) ADJACENT TO THE PH DOMAIN

      FEBS letters
    93. EVENGARD B; SANDSTEDT K; BOLSKE G; FEINSTEIN R; RIESENFELTORN I; SMITH CIE
      INTRANASAL INOCULATION OF MYCOPLASMA-PULMONIS IN MICE WITH SEVERE COMBINED IMMUNODEFICIENCY (SCID) CAUSES A WASTING DISEASE WITH GRAVE ARTHRITIS

      Clinical and experimental immunology
    94. ISLAM KB; BASKIN B; CHRISTENSSON B; HAMMARSTROM L; SMITH CIE
      IN-VIVO EXPRESSION OF HUMAN-IMMUNOGLOBULIN GERM-LINE MESSENGER-RNA INNORMAL AND IN IMMUNODEFICIENT INDIVIDUALS

      Clinical and experimental immunology
    95. BJORKSTRAND B; DILBER MS; SMITH CIE; GAHRTON G; XANTHOPOULOS KG
      RETROVIRAL-MEDIATED GENE-TRANSFER INTO HUMAN MYELOMA CELLS

      British Journal of Haematology
    96. MERUP M; JULIUSSON G; HAMMARSTROM L; SMITH CIE; GAHRTON G
      T-CELL RECEPTOR-BETA GENE REARRANGEMENTS IN LEUKEMIC B-CELLS FROM PATIENTS WITH CHRONIC LYMPHOCYTIC-LEUKEMIA - ASSOCIATION WITH CHROMOSOME-6 DELETIONS

      British Journal of Haematology
    97. MERUP M; JULIUSSON G; SMITH CIE; GAHRTON G
      BCL-2 REARRANGEMENT INVOLVING VARIANT AND MAJOR BREAKPOINT REGIONS INLOW-GRADE AND HIGH-GRADE NON-HODGKIN-LYMPHOMA

      Blood
    98. VIHINEN M; NILSSON L; SMITH CIE
      STRUCTURAL BASIS OF SH2 DOMAIN MUTATIONS IN X-LINKED AGAMMAGLOBULINEMIA

      Biochemical and biophysical research communications
    99. HAMMARSTROM L; GILLNER M; SMITH CIE
      MOLECULAR-BASIS FOR HUMAN IMMUNODEFICIENCIES

      Current opinion in immunology
    100. RABBANI H; DEBOER M; AHLIN A; SUNDIN U; ELINDER G; HAMMARSTROM L; PALMBLAD J; SMITH CIE; ROOS D
      A 40-BASE-PAIR DUPLICATION IN THE GP91-PHOX GENE LEADING TO X-LINKED CHRONIC GRANULOMATOUS-DISEASE

      European journal of haematology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/10/20 alle ore 03:41:37