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Results:
1-15
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Results: 15
Authors:
BRENN T
FRANKE U
FURTHMAYR H
Citation: T. Brenn et al., IN-VITRO FIBRILLIN ASSEMBLY AND BIOSYNTHETIC ABNORMALITIES OF FIBRILLIN IN THE MARFAN-SYNDROME, Journal of the American College of Cardiology, 29(2), 1997, pp. 41146-41146
Authors:
BRENN T
Citation: T. Brenn, ADULT FAMILY MEMBERS AND THEIR RESEMBLANCE OF CORONARY HEART-DISEASE RISK-FACTORS - THE CARDIOVASCULAR-DISEASE STUDY IN FINNMARK, European journal of epidemiology, 13(6), 1997, pp. 623-630
Authors:
THUNE I
BRENN T
LUNK E
GAARD M
Citation: I. Thune et al., PHYSICAL-ACTIVITY AND THE RISK OF BREAST-CANCER, The New England journal of medicine, 336(18), 1997, pp. 1269-1275
Authors:
NILSSEN O
LIPTON R
BRENN T
HOYER G
BOIKO E
TKATCHEV A
Citation: O. Nilssen et al., SLEEPING PROBLEMS AT 78 DEGREES NORTH - THE SVALBARD STUDY, Acta psychiatrica Scandinavica, 95(1), 1997, pp. 44-48
Authors:
LIU WG
QIAN CP
COMEAU K
BRENN T
FURTHMAYR H
FRANCKE U
Citation: Wg. Liu et al., MUTANT FIBRILLIN-1 MONOMERS LACKING EGF-LIKE DOMAINS DISRUPT MICROFIBRIL ASSEMBLY AND CAUSE SEVERE MARFAN-SYNDROME, Human molecular genetics, 5(10), 1996, pp. 1581-1587
Authors:
SCHMIDT MC
KLUES HG
VOMDAHL J
BRENN T
HUGEL W
HANRATH P
Citation: Mc. Schmidt et al., INTRACORONARY DOPPLER FLOW VELOCITY-MEASUREMENTS IN 2 PATIENTS WITH SOLITARY CORONARY OSTIUM - IS THERE TRUE OBSTRUCTION, Coronary artery disease, 7(10), 1996, pp. 761-765
Authors:
BRENN T
AOYAMA T
FRANCKE U
FURTHMAYR H
Citation: T. Brenn et al., DERMAL FIBROBLAST-CULTURE AS A MODEL SYSTEM FOR STUDIES OF FIBRILLIN ASSEMBLY AND PATHOGENETIC MECHANISMS - DEFECTS IN DISTINCT GROUPS OF INDIVIDUALS WITH MARFANS-SYNDROME, Laboratory investigation, 75(3), 1996, pp. 389-402
Authors:
HOYER G
NILSSEN O
BRENN T
SCHIRMER H
Citation: G. Hoyer et al., THE SVALBARD STUDY 1988-89 - A UNIQUE SETTING FOR VALIDATION OF SELF-REPORTED ALCOHOL-CONSUMPTION, Addiction, 90(4), 1995, pp. 539-544
Authors:
ELDADAH ZA
BRENN T
FURTHMAYR H
DIETZ HC
Citation: Za. Eldadah et al., EXPRESSION OF A MUTANT HUMAN FIBRILLIN ALLELE UPON A NORMAL HUMAN OR MURINE GENETIC BACKGROUND RECAPITULATES A MARFAN CELLULAR PHENOTYPE, The Journal of clinical investigation, 95(2), 1995, pp. 874-880
Authors:
FRANCKE U
LIU W
BRENN T
GASNER C
FURTHMAYR H
Citation: U. Francke et al., MARFAN-SYNDROME RND RELATED CONNECTIVE-TISSUE DISORDERS - EXPRESSION OF FBN1 MUTATIONS AT THE MESSENGER-RNA, PROTEIN AND PHENOTYPIC LEVELS, American journal of human genetics, 57(4), 1995, pp. 33-33
Authors:
SPINAZZOLA RM
LIU W
BRENN T
BIALER MG
FURTHMAYR H
FRANCKE U
Citation: Rm. Spinazzola et al., INFANTILE MARFAN-SYNDROME (IMS) DUE TO DE-NOVO SPLICE-SITE MUTATION IN THE FIBRILLIN GENE, American journal of human genetics, 57(4), 1995, pp. 1324-1324
Authors:
FRANCKE U
BERG MA
TYNAN K
BRENN T
LIU WG
AOYAMA T
GASNER C
MILLER DC
FURTHMAYR H
Citation: U. Francke et al., A GLY1127SER MUTATION IN AN EGF-LIKE DOMAIN OF THE FIBRILLIN-1 GENE IS A RISK FACTOR FOR ASCENDING AORTIC-ANEURYSM AND DISSECTION, American journal of human genetics, 56(6), 1995, pp. 1287-1296
Authors:
RICHARDT G
BRENN T
SEYFARTH M
HAASS M
SCHOMIG E
SCHOMIG A
Citation: G. Richardt et al., DUAL EFFECT OF NICOTINE ON CARDIAC NORADRENALINE RELEASE DURING METABOLIC BLOCKADE, Basic research in cardiology, 89(6), 1994, pp. 524-534
Authors:
BRENN T
Citation: T. Brenn, GENETIC AND ENVIRONMENTAL-EFFECTS ON CORONARY-HEART-DISEASE RISK-FACTORS IN NORTHERN NORWAY - THE CARDIOVASCULAR-DISEASE STUDY IN FINNMARK, Annals of Human Genetics, 58, 1994, pp. 369-379
Authors:
ELDADAH ZA
BRENN T
FURTHMAYR H
DIETZ HC
Citation: Za. Eldadah et al., PRODUCTION OF A MARFAN CELLULAR PHENOTYPE BY EXPRESSING A MUTANT HUMAN FIBRILLIN ALLELE ON A NORMAL HUMAN OR MURINE GENETIC BACKGROUND, American journal of human genetics, 55(3), 1994, pp. 10000004-10000004
Risultati:
1-15
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