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Results: 1-19 |
Results: 19
REDUCED BETA-CELL FUNCTION AND BLOOD-PRESSURE IN CARRIERS OF INTRON-16 -3T VARIANT OF THE SULFONYLUREA RECEPTOR GENE
Authors: THART LM RUIGE JB DEKKER JM NIJPELS G MAASSEN JA HEINE RJ
Citation: Lm. Thart et al., REDUCED BETA-CELL FUNCTION AND BLOOD-PRESSURE IN CARRIERS OF INTRON-16 -3T VARIANT OF THE SULFONYLUREA RECEPTOR GENE, Diabetologia, 41, 1998, pp. 122-122
HETEROPLASMY OF THE MITOCHONDRIAL A3243G MUTATION AND THE PHENOTYPE OF MATERNALLY INHERITED DIABETES AND DEAFNESS
Authors: VANESSEN EHR THART LM JANSEN JJ VANDENOUWELAND JMW MAASSEN JA LEMKES HHPJ
Citation: Ehr. Vanessen et al., HETEROPLASMY OF THE MITOCHONDRIAL A3243G MUTATION AND THE PHENOTYPE OF MATERNALLY INHERITED DIABETES AND DEAFNESS, Diabetologia, 41, 1998, pp. 433-433
THE SULFONYLUREA RECEPTOR INTRON-16 GENE VARIANT ASSOCIATES WITH ELEVATED PROINSULIN TO INSULIN RATIOS AND REDUCED BLOOD-PRESSURE
Authors: THART LM RUIGE JB DEKKER JM NIJPELS G MAASSEN JA HEINE RJ
Citation: Lm. Thart et al., THE SULFONYLUREA RECEPTOR INTRON-16 GENE VARIANT ASSOCIATES WITH ELEVATED PROINSULIN TO INSULIN RATIOS AND REDUCED BLOOD-PRESSURE, Diabetes, 47, 1998, pp. 669-669
MUTATION IN MITOCHONDRIAL TRNA(LEU(UUR)) GENE ASSOCIATED WITH PROGRESSIVE KIDNEY-DISEASE
Authors: JANSEN JJ MAASSEN JA VANDERWOUDE FJ LEMMINK HAJ VANDENOUWELAND JMW THART LM SMEETS HJM BRUIJN JA LEMKES HHPJ
Citation: Jj. Jansen et al., MUTATION IN MITOCHONDRIAL TRNA(LEU(UUR)) GENE ASSOCIATED WITH PROGRESSIVE KIDNEY-DISEASE, Journal of the American Society of Nephrology, 8(7), 1997, pp. 1118-1124
DETECTION OF MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN FIBROBLASTS OFPATIENTS WITH PEARSONS-SYNDROME BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: VANDECORPUT MPC VANDENOUWELAND JMW DIRKS RW THART LM BRUINING GJ MAASSEN JA RAAP AK
Citation: Mpc. Vandecorput et al., DETECTION OF MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN FIBROBLASTS OFPATIENTS WITH PEARSONS-SYNDROME BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION, The Journal of histochemistry and cytochemistry, 45(1), 1997, pp. 55-61
MATERNALLY INHERITED DIABETES AND DEAFNESS - A DIABETIC SUBTYPE ASSOCIATED WITH A MUTATION IN MITOCHONDRIAL-DNA
Authors: MAASSEN JA VANDENOUWELAND JMW THART LM LEMKES HHPJ
Citation: Ja. Maassen et al., MATERNALLY INHERITED DIABETES AND DEAFNESS - A DIABETIC SUBTYPE ASSOCIATED WITH A MUTATION IN MITOCHONDRIAL-DNA, Hormone and Metabolic Research, 29(2), 1997, pp. 50-55
HETEROPLASMY LEVELS OF A MITOCHONDRIAL GENE MUTATION ASSOCIATED WITH DIABETES-MELLITUS DECREASE IN LEUKOCYTE DNA UPON AGING
Authors: THART LM JANSEN JJ LEMKES HHPJ DEKNIJFF P MAASSEN JA
Citation: Lm. Thart et al., HETEROPLASMY LEVELS OF A MITOCHONDRIAL GENE MUTATION ASSOCIATED WITH DIABETES-MELLITUS DECREASE IN LEUKOCYTE DNA UPON AGING, Human mutation, 7(3), 1996, pp. 193-197
THE MOLECULAR-BASIS AND CLINICAL CHARACTERISTICS OF MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD), A RECENTLY RECOGNIZED DIABETIC SUBTYPE
Authors: MAASSEN JA JANSEN JJ KADOWAKI T VANDENOUWELAND JMW THART LM LEMKES HHPJ
Citation: Ja. Maassen et al., THE MOLECULAR-BASIS AND CLINICAL CHARACTERISTICS OF MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD), A RECENTLY RECOGNIZED DIABETIC SUBTYPE, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 104(3), 1996, pp. 205-211
EVALUATION OF THE IMPORTANCE OF MATERNAL HISTORY OF DIABETES AND OF MITOCHONDRIAL VARIATION IN THE DEVELOPMENT OF NIDDM
Authors: MCCARTHY M CASSELL P TRAN T MATHIS L THART LM MAASSEN JA SNEHALATHA C RAMACHANDRAN A VISWANATHAN M HITMAN GA
Citation: M. Mccarthy et al., EVALUATION OF THE IMPORTANCE OF MATERNAL HISTORY OF DIABETES AND OF MITOCHONDRIAL VARIATION IN THE DEVELOPMENT OF NIDDM, Diabetic medicine, 13(5), 1996, pp. 420-428
AN INSULIN-RECEPTOR MUTANT (ASP(707)-]ALA), INVOLVED IN LEPRECHAUNISM, IS PROCESSED AND TRANSPORTED TO THE CELL-SURFACE BUT UNABLE TO BIND INSULIN
Authors: THART LM LINDHOUT D VANDERZON GCM KAYSERILLI H APAK MY KLEIJER WJ VANDERVORM ER MAASSEN JA
Citation: Lm. Thart et al., AN INSULIN-RECEPTOR MUTANT (ASP(707)-]ALA), INVOLVED IN LEPRECHAUNISM, IS PROCESSED AND TRANSPORTED TO THE CELL-SURFACE BUT UNABLE TO BIND INSULIN, The Journal of biological chemistry, 271(31), 1996, pp. 18719-18724
A NATURALLY-OCCURRING INSULIN-RECEPTOR MUTANT (ASP707ALA) IS UNABLE TO BIND INSULIN - TRITON X100 RESTORES INSULIN BINDING AND SIGNALING
Authors: MAASSEN JA THART LM KAYSERILI H LINDHOUT D VANDERZON GCM
Citation: Ja. Maassen et al., A NATURALLY-OCCURRING INSULIN-RECEPTOR MUTANT (ASP707ALA) IS UNABLE TO BIND INSULIN - TRITON X100 RESTORES INSULIN BINDING AND SIGNALING, Diabetes, 45, 1996, pp. 1270-1270
ASSOCIATION OF THE INSULIN-RECEPTOR VARIANT MET-985 WITH HYPERGLYCEMIA AND NON-INSULIN-DEPENDENT DIABETES-MELLITUS IN THE NETHERLANDS - A POPULATION-BASED STUDY
Authors: THART LM STOLK RP HEINE RJ GROBBEE DE VANDERDOES FEE MAASSEN JA
Citation: Lm. Thart et al., ASSOCIATION OF THE INSULIN-RECEPTOR VARIANT MET-985 WITH HYPERGLYCEMIA AND NON-INSULIN-DEPENDENT DIABETES-MELLITUS IN THE NETHERLANDS - A POPULATION-BASED STUDY, American journal of human genetics, 59(5), 1996, pp. 1119-1125
ABSENCE OF THE GLY(40)-SER MUTATION IN THE GLUCAGON RECEPTOR AMONG DIABETIC-PATIENTS IN THE NETHERLANDS
Authors: THART LM STOLK RP JANSEN JJ GROBBEE DE LEMKES HHPJ MAASSEN JA
Citation: Lm. Thart et al., ABSENCE OF THE GLY(40)-SER MUTATION IN THE GLUCAGON RECEPTOR AMONG DIABETIC-PATIENTS IN THE NETHERLANDS, Diabetes care, 18(10), 1995, pp. 1400-1401
CLINICAL PRESENTATION OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL-DNAMUTATION
Authors: JANSEN JJ RUTTEN CFA THART LM MAASSEN JA LEMKES HHPJ
Citation: Jj. Jansen et al., CLINICAL PRESENTATION OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL-DNAMUTATION, Diabetologia, 38, 1995, pp. 75-75
AN INCREASED FREQUENCY OF MET985 INSULIN-RECEPTOR VARIANT IN TYPE-II DIABETIC-PATIENTS
Authors: MAASSEN JA THART LM HEINE RJ STOLK RP FESKENS EJM JANSSEN JJ LEMKES HHPJ
Citation: Ja. Maassen et al., AN INCREASED FREQUENCY OF MET985 INSULIN-RECEPTOR VARIANT IN TYPE-II DIABETIC-PATIENTS, Diabetologia, 38, 1995, pp. 77-77
NATURAL COURSE OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS)
Authors: RASKER SP JANSEN JJ VANDENOUWELAND JMW THART LM MAASSSEN JA LEMKES HHPJ
Citation: Sp. Rasker et al., NATURAL COURSE OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS), Diabetologia, 38, 1995, pp. 78-78
MUTATION IN MITOCHONDRIAL TRANSFER-RNA(LEU(UUR)) GENE ASSOCIATED WITHDIABETES AND SEVERE NONDIABETIC KIDNEY-DISEASE
Authors: LEMKES HHPJ JANSEN JJ VANDENOUWELAND JMW VANDERWOUDE FJ THART LM BRUYN JA MAASSEN JA
Citation: Hhpj. Lemkes et al., MUTATION IN MITOCHONDRIAL TRANSFER-RNA(LEU(UUR)) GENE ASSOCIATED WITHDIABETES AND SEVERE NONDIABETIC KIDNEY-DISEASE, Diabetologia, 38, 1995, pp. 229-229
CLINICAL PRESENTATION OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS)
Authors: LEMKES HHPJ JANSEN NJ RASKER SP THART LM VANDENOUWELAND JMW MAASSEN TA
Citation: Hhpj. Lemkes et al., CLINICAL PRESENTATION OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS), Diabetes, 44, 1995, pp. 233-233
PREVALENCE OF MATERNALLY INHERITED DIABETES AND DEAFNESS IN DIABETIC POPULATIONS IN THE NETHERLANDS
Authors: THART LM LEMKES HHPJ HEINE RJ STOLK RP FESKENS EJM JANSEN JJ VANDERDOES FEE GROBBEE DE KROMHOUT D VANDENOUWELAND JMW MAASSEN JA
Citation: Lm. Thart et al., PREVALENCE OF MATERNALLY INHERITED DIABETES AND DEAFNESS IN DIABETIC POPULATIONS IN THE NETHERLANDS, Diabetologia, 37(11), 1994, pp. 1169-1170
Risultati: 1-19 |