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Results: 1-25 | 26-41
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QUANTIFICATION OF (G)GAMMA-GLOBINS AND (A)GAMMA-GLOBINS BY ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY
Authors: OFORIACQUAH SF GREEN BN WILD BJ LALLOZ MRA LAYTON DM
Citation: Sf. Oforiacquah et al., QUANTIFICATION OF (G)GAMMA-GLOBINS AND (A)GAMMA-GLOBINS BY ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY, INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2(4), 1998, pp. 451-453
OPIATES FOR SICKLE-CELL CRISIS
Authors: LAYTON DM MUFTI GJ
Citation: Dm. Layton et Gj. Mufti, OPIATES FOR SICKLE-CELL CRISIS, Lancet, 351(9120), 1998, pp. 1964-1965
FUNCTIONAL-ROLE OF POLYMORPHIC ENHANCER ELEMENTS ON FETAL HEMOGLOBIN EXPRESSION IN SICKLE-CELL-ANEMIA
Authors: OFORIACQUAH SF LALLOZ MRA ANTONIOU M SERJEANT GR LAYTON DM
Citation: Sf. Oforiacquah et al., FUNCTIONAL-ROLE OF POLYMORPHIC ENHANCER ELEMENTS ON FETAL HEMOGLOBIN EXPRESSION IN SICKLE-CELL-ANEMIA, British Journal of Haematology, 101, 1998, pp. 22-22
INTERETHNIC VARIATION IN PREVALENCE OF MUTATION WITHIN FUNCTIONAL ELEMENTS OF THE TRIOSEPHOSPHATE ISOMERASE GENE PROMOTER
Authors: HUMPHRIES AL ATIONU A LALLOZ MRA WILD BJ LAYTON DM
Citation: Al. Humphries et al., INTERETHNIC VARIATION IN PREVALENCE OF MUTATION WITHIN FUNCTIONAL ELEMENTS OF THE TRIOSEPHOSPHATE ISOMERASE GENE PROMOTER, British Journal of Haematology, 101, 1998, pp. 115-115
PROSPECT FOR ENZYME REPLACEMENT THERAPY IN A RED-CELL ENZYMOPATHY - TRIOSEPHOSPHATE ISOMERASE DEFICIENCY
Authors: ATIONU A HUMPHRIES AL WARLOW J MORGAN J ARYA R LALLOZ MRA BELLINGHAM AJ LAYTON DM
Citation: A. Ationu et al., PROSPECT FOR ENZYME REPLACEMENT THERAPY IN A RED-CELL ENZYMOPATHY - TRIOSEPHOSPHATE ISOMERASE DEFICIENCY, British Journal of Haematology, 101, 1998, pp. 116-116
G6PD-BRIGHTON - A NEW CLASS-I GLUCOSE-6-PHOSPHATE-DEHYDROGENASE VARIANT DUE TO A DELETION IN EXON-13
Authors: MCGONIGLE DP LALLOZ MRA WILD BJ LAYTON DM
Citation: Dp. Mcgonigle et al., G6PD-BRIGHTON - A NEW CLASS-I GLUCOSE-6-PHOSPHATE-DEHYDROGENASE VARIANT DUE TO A DELETION IN EXON-13, British Journal of Haematology, 101, 1998, pp. 117-117
IDENTIFICATION OF NOVEL HEMOGLOBIN-VARIANTS HB HACKNEY ALPHA(27)(GLU-]ALA), HB ST MARYS BETA(101)(GLU-]ALA) BY MASS-SPECTROMETRY
Authors: WILD BJ GREEN BN LALLOZ MRA ERTEN S AMOS RJ HORN J WICKRAMASINGHE SN STEPHENS AD LAYTON DM
Citation: Bj. Wild et al., IDENTIFICATION OF NOVEL HEMOGLOBIN-VARIANTS HB HACKNEY ALPHA(27)(GLU-]ALA), HB ST MARYS BETA(101)(GLU-]ALA) BY MASS-SPECTROMETRY, British Journal of Haematology, 101, 1998, pp. 125-125
MOLECULAR-BASIS FOR VARIABLE CLINICAL EXPRESSION OF WISKOTT-ALDRICH SYNDROME
Authors: THOMPSON LJ LALLOZ MRA HIRST WJR LAYTON DM
Citation: Lj. Thompson et al., MOLECULAR-BASIS FOR VARIABLE CLINICAL EXPRESSION OF WISKOTT-ALDRICH SYNDROME, British Journal of Haematology, 101, 1998, pp. 169-169
NEONATAL HEMOLYTIC-ANEMIA DUE TO DE-NOVO GAMMA-DELTA-BETA-DEGREES THALASSEMIA ASSOCIATED WITH INTACT STRUCTURAL GLOBIN GENES
Authors: OFORIACQUAH SF ERTEN S HO A LAYTON DM
Citation: Sf. Oforiacquah et al., NEONATAL HEMOLYTIC-ANEMIA DUE TO DE-NOVO GAMMA-DELTA-BETA-DEGREES THALASSEMIA ASSOCIATED WITH INTACT STRUCTURAL GLOBIN GENES, British Journal of Haematology, 101, 1998, pp. 171-171
TOPICAL GM-CSF IN THE TREATMENT OF CERVICOFACIAL LYMPHADENITIS DUE TOMYCOBACTERIUM-AVIUM-INTRACELLULARE [MAI]
Authors: MILOJKOVIC D LANGDON JD SMITH P BUCKLEY DA DUVIVIER AWP HOWARD ER LAYTON DM
Citation: D. Milojkovic et al., TOPICAL GM-CSF IN THE TREATMENT OF CERVICOFACIAL LYMPHADENITIS DUE TOMYCOBACTERIUM-AVIUM-INTRACELLULARE [MAI], British Journal of Haematology, 101, 1998, pp. 206-206
EVIDENCE FOR FOUNDER EFFECT OF THE GLU104ASP SUBSTITUTION AND IDENTIFICATION OF NEW MUTATIONS IN TRIOSEPHOSPHATE ISOMERASE DEFICIENCY
Authors: ARYA R LALLOZ MRA BELLINGHAM AJ LAYTON DM
Citation: R. Arya et al., EVIDENCE FOR FOUNDER EFFECT OF THE GLU104ASP SUBSTITUTION AND IDENTIFICATION OF NEW MUTATIONS IN TRIOSEPHOSPHATE ISOMERASE DEFICIENCY, Human mutation, 10(4), 1997, pp. 290-294
PREDOMINANCE OF THE HLA-H CYS282TYR MUTATION IN AUSTRIAN PATIENTS WITH GENETIC HEMOCHROMATOSIS
Authors: DATZ C LALLOZ MRA VOGEL W GRAZIADEI I HACKL F VAUTIER G LAYTON DM MAIERDOBERSBERGER T FERENCI P PENNER E SANDHOFER F BOMFORD A PAULWEBER B
Citation: C. Datz et al., PREDOMINANCE OF THE HLA-H CYS282TYR MUTATION IN AUSTRIAN PATIENTS WITH GENETIC HEMOCHROMATOSIS, Journal of hepatology, 27(5), 1997, pp. 773-779
HOMOZYGOSITY FOR THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE 677 C-]T-MUTATIONS IS A MORE COMMON-CAUSE OF THE BUDD-CHIARI-SYNDROME THAN THE FACTOR-V-LEIDEN Q506-ALLELE
Authors: DEVLIN J LALLOZ MRA ERTEN S VARNAVIDES LA DONALDSON P LAYTON DM
Citation: J. Devlin et al., HOMOZYGOSITY FOR THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE 677 C-]T-MUTATIONS IS A MORE COMMON-CAUSE OF THE BUDD-CHIARI-SYNDROME THAN THE FACTOR-V-LEIDEN Q506-ALLELE, Gastroenterology, 112(4), 1997, pp. 1256-1256
DISSECTING THE GENETIC-CONTROL OF FETAL HEMOGLOBIN IN SICKLE-CELL-ANEMIA
Authors: OFORIACQUAH SF LALLOZ MRA ERTEN S GREEN BN WILD BW SERJEANT GR LAYTON DM
Citation: Sf. Oforiacquah et al., DISSECTING THE GENETIC-CONTROL OF FETAL HEMOGLOBIN IN SICKLE-CELL-ANEMIA, Blood, 90(10), 1997, pp. 1967-1967
FAMILY STUDIES IN WISKOTT-ALDRICH SYNDROME BY ANALYSIS OF A LINKED POLYMORPHIC MARKER AT LOCUS DXS6940
Authors: THOMPSON LJ LALLOZ MRA LAYTON DM
Citation: Lj. Thompson et al., FAMILY STUDIES IN WISKOTT-ALDRICH SYNDROME BY ANALYSIS OF A LINKED POLYMORPHIC MARKER AT LOCUS DXS6940, British Journal of Haematology, 93, 1996, pp. 31-31
HOMOZYGOSITY FOR THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE-677 C-]T MUTATION IN BUDD-CHIARI SYNDROME
Authors: LALLOZ MRA DEVLIN J ERTEN S VARNAVIDES LA DONALDSON P WILLIAMS R LAYTON DM
Citation: Mra. Lalloz et al., HOMOZYGOSITY FOR THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE-677 C-]T MUTATION IN BUDD-CHIARI SYNDROME, British Journal of Haematology, 93, 1996, pp. 111-111
PURE RED-CELL APLASIA FOLLOWING AEROSOL INHALATION
Authors: PARKER JE LAYTON DM
Citation: Je. Parker et Dm. Layton, PURE RED-CELL APLASIA FOLLOWING AEROSOL INHALATION, British Journal of Haematology, 93, 1996, pp. 137-137
EVIDENCE FOR FOUNDER EFFECT IN TRIOSEPHOSPHATE ISOMERASE DEFICIENCY DUE TO GLU104ASP MUTATION
Authors: ARYA R LALLOZ MRA BELLINGHAM AJ LAYTON DM
Citation: R. Arya et al., EVIDENCE FOR FOUNDER EFFECT IN TRIOSEPHOSPHATE ISOMERASE DEFICIENCY DUE TO GLU104ASP MUTATION, British Journal of Haematology, 93, 1996, pp. 195-195
DEVELOPMENTAL STAGE-SPECIFIC EXPRESSION OF GLOBIN GENES IN ERYTHROID-CELLS DERIVED FROM THE EXTRAEMBRYONIC COELOM
Authors: OFORIACQUAH SF ROSS J JURKOVIC D LALLOZ MRA CAMPBELL S LAYTON DM
Citation: Sf. Oforiacquah et al., DEVELOPMENTAL STAGE-SPECIFIC EXPRESSION OF GLOBIN GENES IN ERYTHROID-CELLS DERIVED FROM THE EXTRAEMBRYONIC COELOM, British Journal of Haematology, 93, 1996, pp. 197-197
MOLECULAR-BASIS OF SEVERE PYRUVATE-KINASE DEFICIENCY
Authors: LAYTON DM KANNO H ARYA R MCGONIGLE D WILD B COLVIN BT FUJII H MIWA S BELLINGHAM AJ
Citation: Dm. Layton et al., MOLECULAR-BASIS OF SEVERE PYRUVATE-KINASE DEFICIENCY, British Journal of Haematology, 93, 1996, pp. 323-323
EFFECT OF HISTONE DEACETYLASE INHIBITOR TRICHOSTATIN-A ON GAMMA-GLOBIN GENE-EXPRESSION TN K562 CELLS
Authors: OFORIACQUAH SF LALLOZ MRA LAYTON DM
Citation: Sf. Oforiacquah et al., EFFECT OF HISTONE DEACETYLASE INHIBITOR TRICHOSTATIN-A ON GAMMA-GLOBIN GENE-EXPRESSION TN K562 CELLS, British Journal of Haematology, 93, 1996, pp. 335-335
2 NOVEL MUTATIONS IN THE REDUCED NICOTINAMIDE ADENINE-DINUCLEOTIDE (NADH) CYTOCHROME B5 REDUCTASE GENE OF A PATIENT WITH GENERALIZED TYPE, HEREDITARY METHEMOGLOBINEMIA
Authors: MANABE J ARYA R SUMIMOTO H YUBISUI T BELLINGHAM AJ LAYTON DM FUKUMAKI Y
Citation: J. Manabe et al., 2 NOVEL MUTATIONS IN THE REDUCED NICOTINAMIDE ADENINE-DINUCLEOTIDE (NADH) CYTOCHROME B5 REDUCTASE GENE OF A PATIENT WITH GENERALIZED TYPE, HEREDITARY METHEMOGLOBINEMIA, Blood, 88(8), 1996, pp. 3208-3215
STRUCTURAL-ANALYSIS OF HUMAN TRIOSEPHOSPHATE ISOMERASE (TPI) MUTANTS
Authors: ARYA R RINGE D LALLOZ MRA BELLINGHAM AJ LAYTON DM
Citation: R. Arya et al., STRUCTURAL-ANALYSIS OF HUMAN TRIOSEPHOSPHATE ISOMERASE (TPI) MUTANTS, Blood, 88(10), 1996, pp. 1209-1209
LOCALIZATION OF CIS-ACTIVE DETERMINANTS OF FETAL HEMOGLOBIN LEVEL IN SICKLE-CELL-ANEMIA
Authors: OFORIACQUAH SF LALLOZ MRA LAYTON DM
Citation: Sf. Oforiacquah et al., LOCALIZATION OF CIS-ACTIVE DETERMINANTS OF FETAL HEMOGLOBIN LEVEL IN SICKLE-CELL-ANEMIA, Blood, 88(10), 1996, pp. 1960-1960
MOLECULAR DIAGNOSIS OF WISKOTT-ALDRICH SYNDROME IN NORTHERN EUROPEAN KINDREDS
Authors: THOMPSON LJ LALLOZ MRA LAYTON DM
Citation: Lj. Thompson et al., MOLECULAR DIAGNOSIS OF WISKOTT-ALDRICH SYNDROME IN NORTHERN EUROPEAN KINDREDS, Blood, 88(10), 1996, pp. 2003-2003
Risultati: 1-25 | 26-41