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    1. Garcia, CK; Mues, G; Liao, YL; Hyatt, T; Patil, N; Cohen, JC; Hobbs, HH
      Sequence diversity in genes of lipid metabolism

      GENOME RESEARCH
    2. Nelson, MR; Kardia, SLR; Ferrell, RE; Sing, CF
      A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation

      GENOME RESEARCH
    3. Heath, KE; Humphries, SE; Middleton-Price, H; Boxer, M
      A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Stefanutti, C; Di Giacomo, S; Vivenzio, A; Colloridi, V; Bosco, G; Berni, A; Rabbone, I; Cerutti, F; Bertolini, S
      Low-density lipoprotein apheresis in a patient aged 3.5 years

      ACTA PAEDIATRICA
    5. Scheuner, MT
      Genetic predisposition to coronary artery disease

      CURRENT OPINION IN CARDIOLOGY
    6. Demetriou, K; H'Maltezou, E; Pierides, AM
      Familial homozygous hypercholesterolemia: Effective long-term treatment with cascade double filtration plasmapheresis

      BLOOD PURIFICATION
    7. Real, JT; Chaves, FJ; Martinez-Uso, I; Garcia-Garcia, AB; Ascaso, JF; Carmena, R
      Importance of HDL cholesterol levels and the total/HDL cholesterol ratio as a risk factor for coronary heart disease in molecularly defined heterozygous familial hypercholesterolaemia

      EUROPEAN HEART JOURNAL
    8. Cantafora, A; Blotta, I; Bruzzese, N; Calandra, S; Bertolini, S
      Rapid sizing of microsatellite alleles by gel electrophoresis on microfabricated channels: Application to the D19S394 tetranucleotide repeat for cosegregation study of familial hypercholesterolemia

      ELECTROPHORESIS
    9. Sebestjen, M; Zegura, B; Guzic-Salobir, B; Keber, I
      Fibrinolytic parameters and insulin resistance in young survivors myocardial infarction with heterozygous familial hypercholesterolemia

      WIENER KLINISCHE WOCHENSCHRIFT
    10. Real, JT; Chaves, FJ; Civera, M; Garcia-Garcia, AB; Ascaso, JF; Armengod, ME; Carmena, R
      Influence of FH Valencia 1 and 2 mutations of the LDL receptor gene on theresponse to simvastatin in subjects with molecularly defined heterozygous familial hypercholesterolemia in Spain

      MEDICINA CLINICA
    11. Pocsai, Z; Paragh, G; Adany, R
      Multiplex PCR assay for screening deletions in the low density lipoproteinreceptor gene

      CLINICA CHIMICA ACTA
    12. Eden, ER; Naoumova, RP; Burden, JJ; McCarthy, MI; Soutar, AK
      Use of homozygosity mapping to identify a region on chromosome 1 bearing adefective gene that causes autosomal recessive homozygous hypercholesterolemia in two unrelated families

      AMERICAN JOURNAL OF HUMAN GENETICS
    13. Nakajima, T; Iwaki, K; Hamakubo, T; Kodama, T; Emi, M
      Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase: comparison of exon/intron organization of sterol-sensing domains among four related genes

      JOURNAL OF HUMAN GENETICS
    14. Kang, S; Davis, RA
      Cholesterol and hepatic lipoprotein assembly and secretion

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    15. Bertolini, S; Cantafora, A; Averna, M; Cortese, C; Motti, C; Martini, S; Pes, G; Postiglione, A; Stefanutti, C; Blotta, I; Pisciotta, L; Rolleri, M; Langheim, S; Ghisellini, M; Rabbone, I; Calandra, S
      Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    16. Vuorio, AF; Gylling, H; Turtola, H; Kontula, K; Ketonen, P; Miettinen, TA
      Stanol ester margarine alone and with simvastatin lowers serum cholesterolin families with familial hypercholesterolemia caused by the FH-North Karelia mutation

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    17. Imperatore, G; Knowler, WC; Pettitt, DJ; Kobes, S; Fuller, JH; Bennett, PH; Hanson, RL
      A locus influencing total serum cholesterol on chromosome 19p - Results from an autosomal genomic scan of serum lipid concentrations in Pima Indians

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    18. Jensen, JM; Gerdes, LU; Jensen, HK; Christiansen, TM; Brorholt-Petersen, JU; Faergeman, O
      Association of coronary heart disease with age-adjusted aortocoronary calcification in patients with familial hypercholesterolaemia

      JOURNAL OF INTERNAL MEDICINE
    19. Thiart, R; Varret, M; Lintott, CJ; Scott, RS; Loubser, O; du Plessis, L; de Villiers, JNP; Boileau, C; Kotze, MJ
      Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia

      MOLECULAR AND CELLULAR PROBES
    20. Corella, D; Guillen, M; Portoles, O; Sabater, A; Cortina, S; Folch, J; Saiz, C
      Apolipoprotein E polymorphisms and risk of hypercholesterolemia: a case-control study in a working population from Valencia, Spain

      MEDICINA CLINICA
    21. Makar, RSJ; Lipsky, PE; Cuthbert, JA
      Multiple mechanisms, independent of sterol regulatory element binding proteins, regulate low density lipoprotein gene transcription

      JOURNAL OF LIPID RESEARCH
    22. Salazar, LA; Hirata, MH; Giannini, SD; Forti, N; Diament, J; Lima, TM; Hirata, RDC
      Seven DNA polymorphisms at the candidate genes of atherosclerosis in Brazilian women with angiographically documented coronary artery disease

      CLINICA CHIMICA ACTA
    23. Knoblauch, H; Muller-Myhsok, B; Busjahn, A; Ben Avi, L; Bahring, S; Baron, H; Heath, SC; Uhlmann, R; Faulhaber, HD; Shpitzen, S; Aydin, A; Reshef, A; Rosenthal, M; Eliav, O; Muhl, A; Lowe, A; Schurr, D; Harats, D; Jeschke, E; Friedlander, Y; Schuster, H; Luft, FC; Leitersdorf, E
      A cholesterol-lowering gene maps to chromosome 13q

      AMERICAN JOURNAL OF HUMAN GENETICS
    24. Thompson, GR
      Poor responders to statins: a potential target for stanol esters

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    25. Deininger, PL; Batzer, MA
      Alu repeats and human disease

      MOLECULAR GENETICS AND METABOLISM
    26. Cheng, S; Grow, MA; Pallaud, C; Klitz, W; Erlich, HA; Visvikis, S; Chen, JJ; Pullinger, CR; Malloy, MJ; Siest, G; Kane, JP
      A multilocus genotyping assay for candidate markers of cardiovascular disease risk

      GENOME RESEARCH
    27. Bertolini, S; Cassanelli, S; Garuti, R; Ghisellini, M; Simone, ML; Rolleri, M; Masturzo, P; Calandra, S
      Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    28. Real, JT; Ascaso, JF; Chaves, FJ; Tenes, S; Priego, MA; Puig, O; Armengod, ME; Carmena, R
      Plasma Lp(a) values in familial hypercholesterolemia and its relation to coronary heart disease

      NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
    29. Ruan, XZ; Varghese, Z; Fernando, R; Powas, SH; Moorhead, JF
      LDL receptor gene expression in human mesangial cells under the influence of calcium channel blockers

      CLINICAL NEPHROLOGY
    30. Alberto, FL; Figueiredo, MS; Zago, MA; Araujo, AG; Dos-Santos, JE
      The Lebanese mutation as an important cause of familial hypercholesterolemia in Brazil

      BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
    31. Williams, RR; Hopkins, PN; Stephenson, S; Wu, L; Hunt, SC
      Primordial prevention of cardiovascular disease through applied genetics

      PREVENTIVE MEDICINE
    32. Lahoz, C; Mostaza, JM
      Familiar hypercholesterolemia. Do we also differ in this?

      MEDICINA CLINICA
    33. Real, JT; Chaves, JF; Ascaso, JF; Armengod, ME; Carmena, R
      Screening of familial defective apo B-100 in subjects with primary hipercholesterolemia: identification of the first affected family in Spain

      MEDICINA CLINICA
    34. Norman, D; Sun, XM; Bourbon, M; Knight, BL; Naoumova, RP; Soutar, AK
      Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia

      JOURNAL OF CLINICAL INVESTIGATION
    35. Graham, CA; McClean, E; Ward, AJM; Beattie, ED; Martin, S; O'Kane, M; Young, IS; Nicholls, DP
      Mutation screening and genotype : phenotype correlation in familial hypercholesterolaemia

      ATHEROSCLEROSIS
    36. Cenarro, A; Casao, E; Civeira, F; Jensen, HK; Faergeman, O; Pocovi, M
      Pl(A1/A2) polymorphism of platelet glycoprotein IIIa and risk of acute coronary syndromes in heterozygous familial hypercholesterolemia

      ATHEROSCLEROSIS
    37. Sun, XM; Soutar, AK
      Expression in vitro of alternatively spliced variants of the messenger RNAfor human apolipoprotein E receptor-2 identified in human tissues by ribonuclease protection assays

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    38. Jensen, HK; Jensen, LG; Holst, HU; Andreasen, PH; Hansen, PS; Larsen, ML; Kolvraa, S; Bolund, L; Gregersen, N; Faergeman, O
      Normolipidemia and hypercholesterolemia in persons heterozygous for the same 1592+5G -> A splice site mutation in the low-density lipoprotein receptor gene

      CLINICAL GENETICS
    39. Bourbon, M; Fowler, AM; Sun, XM; Soutar, AK
      Inheritance of two different alleles of the low-density lipoprotein (LDL)-receptor gene carrying the recurrent Pro664Leu mutation in a patient with homozygous familial hypercholesterolaemia

      CLINICAL GENETICS
    40. Chae, JJ; Kim, SH; Kim, UK; Han, KH; Kim, HS; Kastner, DL; Namkoong, Y; Park, YB; Lee, CC
      Three novel small deletion mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia

      CLINICAL GENETICS
    41. Szalai, C; Csaszar, A; Czinner, A; Palicz, T; Halmos, B; Romics, L
      Genetic investigation of patients with hypercholesterolemia type IIa

      CLINICAL GENETICS
    42. von Kodolitsch, Y; Pyeritz, RE; Rogan, PK
      Splice-site mutations in atherosclerosis candidate genes - Relating individual information to phenotype

      CIRCULATION
    43. Jensen, JM; Kruse, TA; Brorholt-Petersen, JU; Christiansen, TM; Jensen, HK; Kolvraa, S; Faergeman, O
      Linking genotype to aorto-coronary atherosclerosis: a model using familialhypercholesterolemia and aorto-coronary calcification

      ANNALS OF HUMAN GENETICS
    44. PANG CP
      MOLECULAR DIAGNOSTICS FOR CARDIOVASCULAR-DISEASE

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    45. WILLNOW TE
      RECEPTOR-ASSOCIATED PROTEIN (RAP) - A SPECIALIZED CHAPERONE FOR ENDOCYTIC RECEPTORS

      Biological chemistry
    46. COUTURE P; BRUN LD; SZOTS F; LELIEVRE M; GAUDET D; DESPRES JP; SIMARD J; LUPIEN PJ; GAGNE C
      ASSOCIATION OF SPECIFIC LDL RECEPTOR GENE-MUTATIONS WITH DIFFERENTIALPLASMA-LIPOPROTEIN RESPONSE TO SIMVASTATIN IN YOUNG FRENCH-CANADIANS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Arteriosclerosis, thrombosis, and vascular biology
    47. PIMSTONE SN; SUN XM; DUSOUICH C; FROHLICH JJ; HAYDEN MR; SOUTAR AK
      PHENOTYPIC VARIATION IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA - A COMPARISON OF CHINESE PATIENTS WITH THE SAME OR SIMILAR MUTATIONS INTHE LDL RECEPTOR GENE IN CHINA OR CANADA

      Arteriosclerosis, thrombosis, and vascular biology
    48. MAK YT; PANG CP; TOMLINSON B; ZHANG J; CHAN YS; MAK TWL; MASAREI JRL
      MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN CHINESE FAMILIAL HYPERCHOLESTEROLEMIA PATIENTS

      Arteriosclerosis, thrombosis, and vascular biology
    49. MANDELSHTAM M; CHAKIR K; SHEVTSOV S; GOLUBKOV V; SKOBELEVA N; LIPOVETSKY B; KONSTANTINOV V; DENISENKO A; GAITSKHOKI V; SCHWARTZ E
      PREVALENCE OF LITHUANIAN MUTATION AMONG ST.-PETERSBURG JEWS WITH FAMILIAL HYPERCHOLESTEROLEMIA

      Human mutation
    50. NICHOLLS P; YOUNG IS; GRAHAM CA
      GENOTYPE PHENOTYPE CORRELATIONS IN FAMILIAL HYPERCHOLESTEROLEMIA/

      Current opinion in lipidology
    51. SOUTAR AK
      UPDATE ON LOW-DENSITY-LIPOPROTEIN RECEPTOR MUTATIONS

      Current opinion in lipidology
    52. TONSTAD S
      DO GENETIC DETERMINATES OF ISCHEMIC-HEART-DISEASE IMPLY THAT PREVENTION MAY BECOME MORE DIFFICULT

      Journal of internal medicine
    53. LIU SM; LEIBEL RL; CHUA SC
      PARTIAL DUPLICATION IN THE LEPR(DB-PAS) MUTATION IS A RESULT OF UNEQUAL CROSSING-OVER

      Mammalian genome
    54. RUAN XZ; VARGHESE Z; FERNANDO R; MOORHEAD JF
      CYTOKINE REGULATION OF LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE-TRANSCRIPTION IN HUMAN MESANGIAL CELLS

      Nephrology, dialysis, transplantation
    55. HANSEN PS
      FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100

      Danish medical bulletin
    56. ZERBA KE; FERRELL RE; SING CF
      GENETIC-STRUCTURE OF 5 SUSCEPTIBILITY GENE REGIONS FOR CORONARY-ARTERY DISEASE - DISEQUILIBRIA WITHIN AND AMONG REGIONS

      Human genetics
    57. LEREN TP; BAKKEN KS; HOEL V; HJERMANN I; BERG K
      SCREENING FOR MUTATIONS OF THE APOLIPOPROTEIN-B GENE CAUSING HYPOCHOLESTEROLEMIA

      Human genetics
    58. GUDNASON V; ZHOU T; THORMAR K; BAEHRING S; COOPER J; MILLER G; HUMPHRIES SE; SCHUSTER H
      DETECTION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE PVUII INTRON-15 POLYMORPHISM USING THE POLYMERASE-CHAIN-REACTION - ASSOCIATION WITH PLASMA-LIPID TRAITS IN HEALTHY-MEN AND WOMEN

      Disease markers
    59. CIVEIRA F; CASTILLO JJ; CALVO C; FERRANDO J; DEPEDRO C; MARTINEZRODES P; POCOVI M
      ACHILLES-TENDON SIZE BY HIGH-RESOLUTION SONOGRAPHY IN HEALTHY POPULATION - RELATIONSHIP WITH LIPID-LEVELS

      Medicina Clinica
    60. LIPOVETSKY BM; MANDELSHTAM MY; VASILYEVA LE; SHAKIR K; GOLUBKOV VI; SHVETSOV SP; SKOBELEVA NA; KONSTANTINOV VO; DENISENKO AD; GAITSKHOKI VS; SHVARTS EI
      PREVALENCE AND SYMPTOMS OF LITHUANIAN MUTATION IN JEWS WITH HYPERLIPIDEMIA TYPE-II AND THEIR RESPONSE TO FLUVASTATIN TREATMENT

      Kardiologia
    61. HELLEDAY T; ARNAUDEAU C; JENSSEN D
      A PARTIAL HPRT GENE DUPLICATION GENERATED BY NONHOMOLOGOUS RECOMBINATION IN V79 CHINESE-HAMSTER CELLS IS ELIMINATED BY HOMOLOGOUS RECOMBINATION

      Journal of Molecular Biology
    62. SIJBRANDS EJG; LOMBARDI MP; WESTENDORP RGJ; LEUVEN JAG; MEINDERS AE; VANDERLAARSE A; FRANTS RR; HAVEKES LM; SMELT AHM
      SIMILAR RESPONSE TO SIMVASTATIN IN PATIENTS HETEROZYGOUS FOR FAMILIALHYPERCHOLESTEROLEMIA WITH MESSENGER-RNA NEGATIVE AND MESSENGER-RNA POSITIVE MUTATIONS

      Atherosclerosis
    63. Tonstad, S; Joakimsen, O; Stensland-Bugge, E; Ose, L; Bonaa, KH; Leren, TP
      Carotid intima-media thickness and plaque in patients with familial hypercholesterolaemia mutations and control subjects

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    64. WENHAM PR; HADDAD L; PANARELLI M; ASHBY JP; DAY INM; GILES PD; HUMPHRIES SE; PENNEY MD; RAE PWH; WALKER SW
      SIMPLIFIED DETECTION OF A MUTATION CAUSING FAMILIAL HYPERCHOLESTEROLEMIA THROUGHOUT BRITAIN - EVIDENCE FOR AN ORIGIN IN A COMMON DISTANT ANCESTOR

      Annals of clinical biochemistry
    65. MARAIS AD; FIRTH JC; BATEMAN ME; BYRNES P; MARTENS C; MOUNTNEY J
      ATORVASTATIN - AN EFFECTIVE LIPID-MODIFYING AGENT IN FAMILIAL HYPERCHOLESTEROLEMIA

      Arteriosclerosis, thrombosis, and vascular biology
    66. KOIVISTO UM; GYLLING H; MIETTINEN TA; KONTULA K
      FAMILIAL MODERATE HYPERCHOLESTEROLEMIA CAUSED BY ASP235-]GLU MUTATIONOF THE LDL RECEPTOR GENE AND COOCCURRENCE OF A DE-NOVO DELETION OF THE LDL RECEPTOR GENE IN THE SAME FAMILY

      Arteriosclerosis, thrombosis, and vascular biology
    67. HANSEN PS; DEFESCHE JC; KASTELEIN JJP; GERDES LU; FRAZA L; GERDES C; TATO F; JENSEN HK; JENSEN LG; KLAUSEN IC; FAERGEMAN O; SCHUSTER H
      PHENOTYPIC VARIATION IN PATIENTS HETEROZYGOUS FOR FAMILIAL DEFECTIVE APOLIPOPROTEIN-B (FDB) IN 3 EUROPEAN COUNTRIES

      Arteriosclerosis, thrombosis, and vascular biology
    68. SUN XM; PATEL DD; KNIGHT BL; SOUTAR AK
      COMPARISON OF THE GENETIC-DEFECT WITH LDL-RECEPTOR ACTIVITY IN CULTURED-CELLS FROM PATIENTS WITH A CLINICAL-DIAGNOSIS OF HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Arteriosclerosis, thrombosis, and vascular biology
    69. VUORIO AF; TURTOLA H; KONTULA K
      NEONATAL DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN NEWBORNS BORN TO A PARENT WITH A MOLECULARLY DEFINED HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Arteriosclerosis, thrombosis, and vascular biology
    70. CHAISOMCHIT S; TYRRELL DLJ; CHANG LJ
      DEVELOPMENT OF REPLICATIVE AND NONREPLICATIVE HEPATITIS-B VIRUS VECTORS

      Gene therapy
    71. LEREN TP; TONSTAD S; GUNDERSEN KE; BAKKEN KS; RODNINGEN OK; SUNDVOLD H; OSE L; BERG K
      MOLECULAR-GENETICS OF FAMILIAL HYPERCHOLESTEROLEMIA IN NORWAY

      Journal of internal medicine
    72. THIART R; LOUBSER O; DEVILLIERS JNP; SANTOS M; KOTZE MJ
      NOVEL STOP MUTATION CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN A COSTA-RICAN FAMILY

      Molecular and cellular probes
    73. VARRET M; RABES JP; BOILEAU C
      FAMILIAL HYPERCHOLESTEROLEMIA 25 YEARS AF TER .1. LDL RECEPTOR DEFECTS

      MS. Medecine sciences
    74. FERNIE BA; HOBART MJ
      AN UNUSUAL COMBINED INSERTION DELETION POLYMORPHISM IN INTRON-10 OF THE HUMAN-COMPLEMENT C6 GENE/

      Human genetics
    75. GOEL R; SINGH J; KAUL D
      RECEPTOR-C-K DEPENDENT SIGNALING REGULATES THE LDL-RECEPTOR GENE-TRANSCRIPTION

      Molecular and cellular biochemistry
    76. WINDER AF; RICHMOND W; VALLANCE DT
      INVESTIGATION OF DYSLIPIDAEMIAS

      Journal of Clinical Pathology
    77. RAINWATER DL; KAMMERER CM; VANDEBERG JL; HIXSON JE
      CHARACTERIZATION OF THE GENETIC ELEMENTS CONTROLLING LIPOPROTEIN(A) CONCENTRATIONS IN MEXICAN-AMERICANS - EVIDENCE FOR AT LEAST 3 CONTROLLING ELEMENTS LINKED TO LPA, THE LOCUS ENCODING APOLIPOPROTEIN(A)

      Atherosclerosis
    78. VOHL MC; GAUDET D; MOORJANI S; TREMBLAY G; PERRON P; GAGNE C; LESIEGE D; BERGERON J; LUPIEN PJ; DESPRES JP
      COMPARISON OF THE EFFECT OF 2 LOW-DENSITY-LIPOPROTEIN RECEPTOR CLASS MUTATIONS ON CORONARY-HEART-DISEASE AMONG FRENCH-CANADIAN PATIENTS HETEROZYGOUS FOR FAMILIAL HYPERCHOLESTEROLEMIA

      European journal of clinical investigation
    79. VUORIO AF; TURTOLA H; KONTULA K
      A NOVEL POINT MUTATION (PRO84-]SER) OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN A FAMILY WITH MODERATE HYPERCHOLESTEROLEMIA

      Clinical genetics
    80. HUMPHRIES SE; GUDNASON V; WHITTALL R; DAY INM
      SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS WITH HIGH-THROUGHPUTMODIFICATIONS, AND ITS USE IN MUTATION DETECTION IN FAMILIAL HYPERCHOLESTEROLEMIA

      Clinical chemistry
    81. GALTON DJ
      GENETIC-DETERMINANTS OF ATHEROSCLEROSIS-RELATED DYSLIPIDEMIAS AND THEIR CLINICAL IMPLICATIONS

      Clinica chimica acta
    82. TONSTAD S; REFSUM H; UELAND PM
      ASSOCIATION BETWEEN PLASMA TOTAL HOMOCYSTEINE AND PARENTAL HISTORY OFCARDIOVASCULAR-DISEASE IN CHILDREN WITH FAMILIAL HYPERCHOLESTEROLEMIA

      Circulation
    83. ANDERSEN LK; JENSEN HK; JUUL S; FAERGEMAN O
      PATIENTS ATTITUDES TOWARD DETECTION OF HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

      Archives of internal medicine
    84. HADDAD L; DAY LB; ATTWOOD J; POVEY S; HUMPHRIES SE; DAY INM
      DEVELOPMENT OF A MICROSATELLITE-BASED APPROACH TO CO-SEGREGATION ANALYSIS OF FAMILIAL HYPERCHOLESTEROLEMIC KINDREDS

      Annals of Human Genetics
    85. TONSTAD S; SIVERTSEN M
      DIETARY ADHERENCE IN CHILDREN WITH FAMILIAL HYPERCHOLESTEROLEMIA

      The American journal of clinical nutrition
    86. WIERZBICKI AS
      DIAGNOSIS AND MANAGEMENT OF HYPERLIPIDEMIA

      International journal of clinical practice
    87. TONSTAD S; JOAKIMSEN O; STENSLANDBUGGE E; LEREN TP; OSE L; RUSSELL D; BONAA KH
      RISK-FACTORS RELATED TO CAROTID INTIMA-MEDIA THICKNESS AND PLAQUE IN CHILDREN WITH FAMILIAL HYPERCHOLESTEROLEMIA AND CONTROL SUBJECTS

      Arteriosclerosis, thrombosis, and vascular biology
    88. BENLIAN P; DEGENNES JL; DAIROU F; HERMELIN B; GINON I; VILLAIN E; LAGARDE JP; FEDERSPIEL MC; BERTRAND V; BERNARD C; BEREZIAT G
      PHENOTYPIC-EXPRESSION IN DOUBLE HETEROZYGOTES FOR FAMILIAL HYPERCHOLESTEROLEMIA AND FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100

      Human mutation
    89. WEBB JC; PATEL DD; SHOULDERS CC; KNIGHT BL; SOUTAR AK
      GENETIC-VARIATION AT A SPLICING BRANCH POINT IN INTRON-9 OF THE LOW-DENSITY-LIPOPROTEIN (LDL)-RECEPTOR GENE - A RARE MUTATION THAT DISRUPTSMESSENGER-RNA SPLICING IN A PATIENT WITH FAMILIAL HYPERCHOLESTEROLEMIA AND A COMMON POLYMORPHISM

      Human molecular genetics
    90. MOREL DW; LIN CY
      CELLULAR BIOCHEMISTRY OF OXYSTEROLS DERIVED FROM THE DIET OR OXIDATION IN-VIVO

      Journal of nutritional biochemistry
    91. TONSTAD S; OSE L
      COLESTIPOL TABLETS IN ADOLESCENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA

      Acta paediatrica
    92. TONSTAD S
      FAMILIAL HYPERCHOLESTEROLEMIA - A PILOT-STUDY OF PARENTS AND CHILDRENS CONCERNS

      Acta paediatrica
    93. FRIEDLANDER Y; LEITERSDORF E
      INFLUENCE OF APOLIPOPROTEIN-E GENOTYPES ON PLASMA-LIPID AND LIPOPROTEIN CONCENTRATIONS - RESULTS FROM A SEGREGATION ANALYSIS IN PEDIGREES WITH MOLECULARLY DEFINED FAMILIAR HYPERCHOLESTEROLEMIA

      Genetic epidemiology
    94. RESHEF A; NISSEN H; TRIGER L; HENSEN TS; ELIAV O; SCHURR D; SAFADI R; GARE M; LEITERSDORF E
      MOLECULAR-GENETICS OF FAMILIAL HYPERCHOLESTEROLEMIA IN ISRAEL

      Human genetics
    95. GOEL R; VARMA S; KAUL D
      STEROL DEPENDENT LDL-RECEPTOR GENE-TRANSCRIPTION IN LYMPHOCYTES FROM NORMAL AND CML PATIENTS

      Cancer letters
    96. GUEDDARI N; FAVRE G; MARMOUGET C; SOULA G; LEGAILLARD F
      INVOLVEMENT OF TYROSINE KINASE-ACTIVITY IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR EXPRESSION IN HUMAN LUNG ADENOCARCINOMA CELL-LINE A549

      Biochimie
    97. LOPEZCANOVAS L; PEREZ GP; HIGGINSON D; GONZALEZQUEVEDO A; FERNANDEZ R; RIVERON AM
      PVU-II RFLPS OF LDL RECEPTOR GENE IN NORMOLIPIDEMIC SUBJECTS FROM HAVANA-CITY

      Archives of medical research
    98. FEUSSNER G; DOBMEYER J; NISSEN H; HANSEN TS
      UNUSUAL XANTHOMAS IN A YOUNG PATIENT WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA AND TYPE-III HYPERLIPOPROTEINEMIA

      American journal of medical genetics
    99. GOEL R; KAUL D; VARMA S
      LYMPHOCYTES FROM CML PATIENTS LACK A 47 KDA FACTOR HAVING AFFINITY FOR A GENOMIC STEROL REGULATORY SEQUENCE

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/10/20 alle ore 14:48:15