ACNP - Italian Periodicals Catalogue

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Results: 1-25 | 26-41 |

Results: 26-41/41

PHOSPHORYLATION OF THREONINE-558 IN THE CARBOXYL-TERMINAL ACTIN-BINDING DOMAIN OF MOESIN BY THROMBIN ACTIVATION OF HUMAN PLATELETS

Authors: NAKAMURA F AMIEVA MR FURTHMAYR H

Citation: F. Nakamura et al., PHOSPHORYLATION OF THREONINE-558 IN THE CARBOXYL-TERMINAL ACTIN-BINDING DOMAIN OF MOESIN BY THROMBIN ACTIVATION OF HUMAN PLATELETS, The Journal of biological chemistry, 270(52), 1995, pp. 31377-31385

SUBCELLULAR-LOCALIZATION OF MOESIN IN DYNAMIC FILOPODIA, RETRACTION FIBERS, AND OTHER STRUCTURES INVOLVED IN SUBSTRATE EXPLORATION, ATTACHMENT, AND CELL-CELL CONTACTS

Authors: AMIEVA MR FURTHMAYR H

Citation: Mr. Amieva et H. Furthmayr, SUBCELLULAR-LOCALIZATION OF MOESIN IN DYNAMIC FILOPODIA, RETRACTION FIBERS, AND OTHER STRUCTURES INVOLVED IN SUBSTRATE EXPLORATION, ATTACHMENT, AND CELL-CELL CONTACTS, Experimental cell research, 219(1), 1995, pp. 180-196

MARFAN-SYNDROME RND RELATED CONNECTIVE-TISSUE DISORDERS - EXPRESSION OF FBN1 MUTATIONS AT THE MESSENGER-RNA, PROTEIN AND PHENOTYPIC LEVELS

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

INFANTILE MARFAN-SYNDROME (IMS) DUE TO DE-NOVO SPLICE-SITE MUTATION IN THE FIBRILLIN GENE

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

A GLY1127SER MUTATION IN AN EGF-LIKE DOMAIN OF THE FIBRILLIN-1 GENE IS A RISK FACTOR FOR ASCENDING AORTIC-ANEURYSM AND DISSECTION

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

MOESIN AND RADIXIN - CYTOSKELETAL PROTEINS ASSOCIATED WITH MESANGIAL CELL ACTIVATION AND MIGRATION IN-VITRO AND IN DISEASE

Authors: HUGO HC PICHLER R GORDON K HUGO CL FURTHMAYR H JOHNSON RJ

Citation: Hc. Hugo et al., MOESIN AND RADIXIN - CYTOSKELETAL PROTEINS ASSOCIATED WITH MESANGIAL CELL ACTIVATION AND MIGRATION IN-VITRO AND IN DISEASE, Journal of the American Society of Nephrology, 5(3), 1994, pp. 782-782

STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN)

Authors: WILGENBUS KK HSIEH CL LANKES WT MILATOVICH A FRANCKE U FURTHMAYR H

Citation: Kk. Wilgenbus et al., STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN), Genomics, 19(2), 1994, pp. 326-333

MARFANS-SYNDROME AND OTHER DISORDERS OF FIBRILLIN

Authors: FRANCKE U FURTHMAYR H

Citation: U. Francke et H. Furthmayr, MARFANS-SYNDROME AND OTHER DISORDERS OF FIBRILLIN, The New England journal of medicine, 330(19), 1994, pp. 1384-1385

QUANTITATIVE DIFFERENCES IN BIOSYNTHESIS AND EXTRACELLULAR DEPOSITIONOF FIBRILLIN IN CULTURED FIBROBLASTS DISTINGUISH 5 GROUPS OF MARFAN-SYNDROME PATIENTS AND SUGGEST DISTINCT PATHOGENETIC MECHANISMS

Authors: AOYAMA T FRANCKE U DIETZ HC FURTHMAYR H

Citation: T. Aoyama et al., QUANTITATIVE DIFFERENCES IN BIOSYNTHESIS AND EXTRACELLULAR DEPOSITIONOF FIBRILLIN IN CULTURED FIBROBLASTS DISTINGUISH 5 GROUPS OF MARFAN-SYNDROME PATIENTS AND SUGGEST DISTINCT PATHOGENETIC MECHANISMS, The Journal of clinical investigation, 94(1), 1994, pp. 130-137

RADIXIN IS A COMPONENT OF HEPATOCYTE MICROVILLI IN-SITU

Authors: AMIEVA MR WILGENBUS KK FURTHMAYR H

Citation: Mr. Amieva et al., RADIXIN IS A COMPONENT OF HEPATOCYTE MICROVILLI IN-SITU, Experimental cell research, 210(1), 1994, pp. 140-144

QUANTITATIVE DIFFERENCES IN BIOSYNTHESIS AND EXTRACELLULAR DEPOSITIONOF FIBRILLIN IN CULTURED FIBROBLASTS DISTINGUISH 5 GROUPS OF MARFAN-SYNDROME PATIENTS

Authors: AOYAMA T FRANCKE U DIETZ HC FURTHMAYR H

QUANTITATIVE DIFFERENCES IN BIOSYNTHESIS AND EXTRACELLULAR DEPOSITIONOF FIBRILLIN IN CULTURED FIBROBLASTS DISTINGUISH 5 GROUPS OF MARFAN-SYNDROME PATIENTS

Authors: AOYAMA T FRANCKE U DIETZ HC FURTHMAYR H

PRODUCTION OF A MARFAN CELLULAR PHENOTYPE BY EXPRESSING A MUTANT HUMAN FIBRILLIN ALLELE ON A NORMAL HUMAN OR MURINE GENETIC BACKGROUND

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

MISSENSE MUTATIONS IMPAIR INTRACELLULAR PROCESSING OF FIBRILLIN AND MICROFIBRIL ASSEMBLY IN MARFAN-SYNDROME

Authors: AOYAMA T TYNAN K DIETZ HC FRANCKE U FURTHMAYR H

Citation: T. Aoyama et al., MISSENSE MUTATIONS IMPAIR INTRACELLULAR PROCESSING OF FIBRILLIN AND MICROFIBRIL ASSEMBLY IN MARFAN-SYNDROME, Human molecular genetics, 2(12), 1993, pp. 2135-2140

CLONING AND SEQUENCING OF PORCINE MOESIN AND RADIXIN CDNA AND IDENTIFICATION OF HIGHLY CONSERVED DOMAINS

Authors: LANKES WT SCHWARTZALBIEZ R FURTHMAYR H

Citation: Wt. Lankes et al., CLONING AND SEQUENCING OF PORCINE MOESIN AND RADIXIN CDNA AND IDENTIFICATION OF HIGHLY CONSERVED DOMAINS, Biochimica et biophysica acta, 1216(3), 1993, pp. 479-482

AORTIC-ANEURYSM IN A FAMILY WITH A GLYCINE-TO-SERINE SUBSTITUTION IN THE FBN-1 GENE

Authors: BERG MA TYNAN K AOYAMA T GASNER C COMEAU K PEARSON M LEVITT D ALCORN D MILLER C FURTHMAYR H FRANCKE U

Citation: Ma. Berg et al., AORTIC-ANEURYSM IN A FAMILY WITH A GLYCINE-TO-SERINE SUBSTITUTION IN THE FBN-1 GENE, American journal of human genetics, 53(3), 1993, pp. 151-151

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