K Asselta: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

51

THE PROPHYLAXIS OF CHOLERA BY INOCULATION.

Llope, W.J., Zhou, J., Nussbaum, T., Hoffmann, G.W., Asselta, K., Brandenburg, J.D., Butterworth, J., Camarda, T., Christie, W., Crawford, H.J., Dong, X., Engelage, J., Eppley, G., Geurts, F., Hammond

Journal:

Year:

1913

Language:

english

File:

PDF, 364 KB

english, 1913

52

Effect of an Interactive Surface on the Equilibrium Contact Angles in Bilayer Polymer Films

Slep, D., Asselta, J., Rafailovich, M. H., Sokolov, J., Winesett, D. A., Smith, A. P., Ade, H., Anders, Simone

Journal:

Year:

2000

Language:

english

File:

PDF, 157 KB

english, 2000

53

Phase Separation of Polystyrene and Bromo−Polystyrene Mixtures in Equilibrium Structures in Thin Films

Slep, D., Asselta, J., Rafailovich, M. H., Sokolov, J., Winesett, D. A., Smith, A. P., Ade, H., Strzhemechny, Y., Schwarz, S. A., Sauer, B. B.

Journal:

Year:

1998

Language:

english

File:

PDF, 133 KB

english, 1998

54

Glucocerebrosidase mutations in primary parkinsonism

Asselta, Rosanna, Rimoldi, Valeria, Siri, Chiara, Cilia, Roberto, Guella, Ilaria, Tesei, Silvana, Soldà, Giulia, Pezzoli, Gianni, Duga, Stefano, Goldwurm, Stefano

Journal:

Parkinsonism & Related Disorders

Year:

2014

Language:

english

File:

PDF, 386 KB

english, 2014

55

No association of GBA mutations and multiple system atrophy

Srulijes, K., Hauser, A. -K., Guella, I., Asselta, R., Brockmann, K., Schulte, C., Soldà, G., Cilia, R., Maetzler, W., Schols, L., Wenning, G. K., Poewe, W., Barone, P., Wüllner, U., Oertel, W., Berg,

Journal:

European Journal of Neurology

Year:

2013

Language:

english

File:

PDF, 432 KB

english, 2013

56

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange

Journal:

Year:

2014

Language:

english

File:

PDF, 375 KB

english, 2014

57

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women

Biguzzi, E., Franchi, F., Acaia, B., Ossola, W., Nava, U., Paraboschi, E. M., Asselta, R., Peyvandi, F.

Journal:

Year:

2014

Language:

english

File:

PDF, 116 KB

english, 2014

58

Perspectives of a mid-rapidity dimuon program at the RHIC: a novel and compact muon telescope detector

Ruan, L, Lin, G, Xu, Z, Asselta, K, Chen, H F, Christie, W, Crawford, H J, Engelage, J, Eppley, G, Hallman, T J, Li, C, Liu, J, Llope, W J, Majka, R, Nussbaum, T, Scheblein, J, Shao, M, Soja, R, Sun,

Journal:

Journal of Physics G Nuclear and Particle Physics

Year:

2009

Language:

english

File:

PDF, 1.89 MB

english, 2009

59

A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

Solda, G., Robusto, M., Primignani, P., Castorina, P., Benzoni, E., Cesarani, A., Ambrosetti, U., Asselta, R., Duga, S.

Journal:

Human Molecular Genetics

Year:

2012

Language:

english

File:

PDF, 390 KB

english, 2012

60

Missense or splicing mutation? The case of a fibrinogen B -chain mutation causing severe hypofibrinogenemia

Journal:

Year:

2004

Language:

english

File:

PDF, 184 KB

english, 2004

61

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern

Dall'Osso, C., Guella, I., Duga, S., Locatelli, N., Paraboschi, E. M., Spreafico, M., Afrasiabi, A., Pechlaner, C., Peyvandi, F., Tenchini, M. L., Asselta, R.

Journal:

Year:

2008

Language:

english

File:

PDF, 337 KB

english, 2008

62

Association and Functional Analyses of MEF2A as a Susceptibility Gene for Premature Myocardial Infarction and Coronary Artery Disease

Guella, I., Rimoldi, V., Asselta, R., Ardissino, D., Francolini, M., Martinelli, N., Girelli, D., Peyvandi, F., Tubaro, M., Merlini, P. A., Mannucci, P. M., Duga, S.

Journal:

Circulation Cardiovascular Genetics

Year:

2009

Language:

english

File:

PDF, 852 KB

english, 2009

63

Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population

Guella, I., Asselta, R., Ardissino, D., Merlini, P. A., Peyvandi, F., Kathiresan, S., Mannucci, P. M., Tubaro, M., Duga, S.

Journal:

The Journal of Lipid Research

Year:

2010

Language:

english

File:

PDF, 1008 KB

english, 2010

64

Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy

Sogno Valin, Paola, Proverbio, Maria Carla, Diceglie, Cecilia, Gessi, Alessandra, di Candia, Stefania, Mariani, Benedetta, Zamproni, Ilaria, Mangano, Eleonora, Asselta, Rosanna, Battaglia, Cristina, C

Journal:

Hormone Research in Paediatrics

Year:

2013

Language:

english

File:

PDF, 456 KB

english, 2013

65

Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation

Asselta, Rosanna, Robusto, Michela, Platé, Manuela, Santoro, Cristina, Peyvandi, Flora, Duga, Stefano

Journal:

Thrombosis Research

Year:

2015

Language:

english

File:

PDF, 741 KB

english, 2015

66

The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy

Robusto, Michela, Fang, Mingyan, Asselta, Rosanna, Castorina, Pierangela, Previtali, Stefano C, Caccia, Sonia, Benzoni, Elena, De Cristofaro, Raimondo, Yu, Cong, Cesarani, Antonio, Liu, Xuanzhu, Li, W

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.50 MB

english, 2015

67

Genetic Association and Altered Gene Expression of Mir-155 in Multiple Sclerosis Patients

Paraboschi, Elvezia Maria, Soldà, Giulia, Gemmati, Donato, Orioli, Elisa, Zeri, Giulia, Benedetti, Maria Donata, Salviati, Alessandro, Barizzone, Nadia, Leone, Maurizio, Duga, Stefano, Asselta, Rosann

Journal:

International Journal of Molecular Sciences

Year:

2011

Language:

english

File:

PDF, 486 KB

english, 2011

68

PRKCA and Multiple Sclerosis: Association in Two Independent Populations

Saarela, Janna, Kallio, Suvi P., Chen, Daniel, Montpetit, Alexandre, Jokiaho, Anne, Choi, Eva, Asselta, Rosanna, Bronnikov, Denis, Lincoln, Matthew R., Sadovnick, A. Dessa, Tienari, Pentti J., Koivist

Journal:

Year:

2006

Language:

english

File:

PDF, 586 KB

english, 2006

69

Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction

Thormaehlen, Aenne S., Schuberth, Christian, Won, Hong-Hee, Blattmann, Peter, Joggerst-Thomalla, Brigitte, Theiss, Susanne, Asselta, Rosanna, Duga, Stefano, Merlini, Pier Angelica, Ardissino, Diego, L

Journal:

Year:

2015

Language:

english

File:

PDF, 1.31 MB

english, 2015

70

Phase behavior and critical activated dynamics of limited-valence DNA nanostars

Biffi, S., Cerbino, R., Bomboi, F., Paraboschi, E. M., Asselta, R., Sciortino, F., Bellini, T.

Journal:

Proceedings of the National Academy of Sciences

Year:

2013

Language:

english

File:

PDF, 870 KB

english, 2013

71

Factor V Deficiency

Asselta, Rosanna, Peyvandi, Flora

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2009

Language:

english

File:

PDF, 199 KB

english, 2009

72

First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family

Soldà, Giulia, Caccia, Sonia, Robusto, Michela, Chiereghin, Chiara, Castorina, Pierangela, Ambrosetti, Umberto, Duga, Stefano, Asselta, Rosanna

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 807 KB

english, 2015

73

Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene

Costantino, Lucy, Rusconi, Damiana, Soldà, Giulia, Seia, Manuela, Paracchini, Valentina, Porcaro, Luigi, Asselta, Rosanna, Colombo, Carla, Duga, Stefano

Journal:

American Journal of Respiratory Cell and Molecular Biology

Year:

2013

Language:

english

File:

PDF, 1.16 MB

english, 2013

74

Understanding the differential regulation of GBA and GBAP1 expression

Rimoldi, Valeria, Rovaris, Giulia, Straniero, Letizia, Pezzoli, Gianni, Goldwurm, Stefano, Soldà, Giulia, Asselta, Rosanna, Duga, Stefano

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 55 KB

english, 2016

75

In vitro assessment of mitral valve function in cyclically pressurized porcine hearts

Vismara, Riccardo, Leopaldi, Alberto M., Piola, Marco, Asselta, Chiara, Lemma, Massimo, Antona, Carlo, Redaelli, Alberto, van de Vosse, Frans, Rutten, Marcel, Fiore, Gianfranco B.

Journal:

Medical Engineering & Physics

Year:

2016

Language:

english

File:

PDF, 2.88 MB

english, 2016

76

Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE

Bonati, Maria Teresa, Asselta, Rosanna, Duga, Stefano, Ferini-Strambi, Luigi, Oldani, Alessandro, Zucconi, Marco, Malcovati, Massimo, Dalprà, Leda, Tenchini, Maria Luisa

Journal:

Year:

2000

Language:

english

File:

PDF, 154 KB

english, 2000

77

Identification of novel PD genes by whole-exome sequencing in Italian families

Straniero, Letizia, Soldà, Giulia, Asselta, Rosanna, Guella, Ilaria, Pezzoli, Gianni, Farrer, Matthew, Goldwurm, Stefano, Duga, Stefano

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 47 KB

english, 2016

78

Understanding the differential regulation of GBA and GBAP1 expression

Rimoldi, Valeria, Rovaris, Giulia, Straniero, Letizia, Pezzoli, Gianni, Goldwurm, Stefano, Soldà, Giulia, Asselta, Rosanna, Duga, Stefano

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 171 KB

english, 2016

79

Identification of novel PD genes by whole-exome sequencing in Italian families

Straniero, Letizia, Soldà, Giulia, Asselta, Rosanna, Guella, Ilaria, Pezzoli, Gianni, Farrer, Matthew, Goldwurm, Stefano, Duga, Stefano

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 53 KB

english, 2016

80

Tryptophan hydroxylase type 2 variants modulate severity and outcome of addictive behaviors in Parkinson's disease

Cilia, Roberto, Benfante, Roberta, Asselta, Rosanna, Marabini, Laura, Cereda, Emanuele, Siri, Chiara, Pezzoli, Gianni, Goldwurm, Stefano, Fornasari, Diego

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 324 KB

english, 2016

81

Molecular Genetics of Quantitative Fibrinogen Disorders

Asselta, R., Spena, S., Duga, S., Tenchini, M.

Journal:

Cardiovascular & Hematological Agents in Medicinal Chemistry (Formerly Current Medicinal Chemistry - Cardiovascular & Hematological Agents)

Year:

2007

Language:

english

File:

PDF, 674 KB

english, 2007

82

Recurrence of the ‘deep-intronic’ FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of Veneto

Platè, Manuela, Duga, Stefano, Castaman, Giancarlo, Rodeghiero, Francesco, Asselta, Rosanna

Journal:

Blood Coagulation & Fibrinolysis

Year:

2009

Language:

english

File:

PDF, 279 KB

english, 2009

83

Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module

Asselta, R., Robusto, M., Braidotti, P., Peyvandi, F., Nastasio, S., D'Antiga, L., Perisic, V. N., Maggiore, G., Caccia, S., Duga, S.

Journal:

Journal of Thrombosis and Haemostasis

Year:

2015

Language:

english

File:

PDF, 591 KB

english, 2015

84

A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family

Song, Jaewoo, Guella, Ilaria, Kwon, Ki-Yung, Cho, Hyunsoo, Park, Rojin, Asselta, Rosanna, Choi, Jong Rak

Journal:

Blood Coagulation & Fibrinolysis

Year:

2009

Language:

english

File:

PDF, 466 KB

english, 2009

85

Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis

Straniero, Letizia, Soldà, Giulia, Costantino, Lucy, Seia, Manuela, Melotti, Paola, Colombo, Carla, Asselta, Rosanna, Duga, Stefano

Journal:

Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 553 KB

english, 2016

86

Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay

Plate, M., Duga, S., Baronciani, L., La Marca, S., Rubini, V., Mannucci, P. M., Federici, A. B., Asselta, R.

Journal:

Year:

2010

Language:

english

File:

PDF, 213 KB

english, 2010

87

Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians

Zadra, G., Asselta, R., Tenchini, M. L., Castaman, G., Seligsohn, U., Mannucci, P. M., Duga, S.

Journal:

Year:

2008

Language:

english

File:

PDF, 275 KB

english, 2008

88

miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA

Paraboschi, Elvezia Maria, Cardamone, Giulia, Rimoldi, Valeria, Duga, Stefano, Soldà, Giulia, Asselta, Rosanna

Journal:

Biochimica et Biophysica Acta (BBA) - General Subjects

Year:

2017

Language:

english

File:

PDF, 894 KB

english, 2017

89

Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

Khera, Amit V., Won, Hong-Hee, Peloso, Gina M., O’Dushlaine, Colm, Liu, Dajiang, Stitziel, Nathan O., Natarajan, Pradeep, Nomura, Akihiro, Emdin, Connor A., Gupta, Namrata, Borecki, Ingrid B., Asselta

Journal:

JAMA The Journal of the American Medical Association

Year:

2017

Language:

english

File:

PDF, 328 KB

english, 2017

90

Exploring the global landscape of genetic variation in coagulation factor XI deficiency

Asselta, Rosanna, Paraboschi, Elvezia Maria, Rimoldi, Valeria, Menegatti, Marzia, Peyvandi, Flora, Salomon, Ophira, Duga, Stefano

Journal:

Year:

2017

Language:

english

File:

PDF, 128 KB

english, 2017

91

Opioid K receptor variant is associated with a delayed onset of dyskinesias in Parkinson’s disease

Cilia, Roberto, Asselta, Rosanna, Cereda, Emanuele, Benfante, Roberta, Barbella, Giuseppina, Vallauri, Davide, Marabini, Laura, Fornasari, Diego, Goldwurm, Stefano, Pezzoli, Gianni

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2017

Language:

english

File:

PDF, 435 KB

english, 2017

92

DNAJC12 and dopa-responsive non-progressive Parkinsonism

Straniero, Letizia, Guella, Ilaria, Cilia, Roberto, Parkkinen, Laura, Rimoldi, Valeria, Young, Alexander, Asselta, Rosanna, Soldà, Giulia, Sossi, Vesna, Stoessl, A. Jon, Priori, Alberto, Nishioka, Ken

Journal:

Annals of Neurology

Year:

2017

Language:

english

File:

PDF, 1.56 MB

english, 2017

93

The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p

Straniero, Letizia, Rimoldi, Valeria, Samarani, Maura, Goldwurm, Stefano, Di Fonzo, Alessio, Krüger, Rejko, Deleidi, Michela, Aureli, Massimo, Soldà, Giulia, Duga, Stefano, Asselta, Rosanna

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 2.56 MB

english, 2017

94

Molecular investigation of 41 patients affected by coagulation factor XI deficiency

Rimoldi, V., Paraboschi, E. M., Menegatti, M., Peyvandi, F., Salomon, O., Duga, S., Asselta, R.

Journal:

Year:

2017

Language:

english

File:

PDF, 504 KB

english, 2017

95

Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency

Asselta, Rosanna, Platè, Manuela, Robusto, Michela, Borhany, Munira, Guella, Ilaria, Soldà, Giulia, Afrasiabi, Abdolreza, Menegatti, Marzia, Tahir, Shamsi, Peyvandi, Flora, Duga, Stefano

Journal:

Thrombosis and Haemostasis

Year:

2015

Language:

english

File:

PDF, 648 KB

english, 2015

96

Newtonian to non-Newtonian fluid transition of a model transient network

Nava, Giovanni, Tie, Yang, Vitali, Valerio, Minzioni, Paolo, Cristiani, Ilaria, Bragheri, Francesca, Osellame, Roberto, Bethge, Lucas, Klussmann, Sven, Paraboschi, Elvezia Maria, Asselta, Rosanna, Bel

Journal:

Year:

2018

Language:

english

File:

PDF, 704 KB

english, 2018

97

Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript

Rimoldi, Valeria, Soldà, Giulia, Asselta, Rosanna, Spena, Silvia, Stuani, Cristiana, Buratti, Emanuele, Duga, Stefano, Bardoni, Barbara

Journal:

Year:

2013

Language:

english

File:

PDF, 1.20 MB

english, 2013

98

Whole Genome SNP Genotyping and Exome Sequencing Reveal Novel Genetic Variants and Putative Causative Genes in Congenital Hyperinsulinism

Proverbio, Maria Carla, Mangano, Eleonora, Gessi, Alessandra, Bordoni, Roberta, Spinelli, Roberta, Asselta, Rosanna, Valin, Paola Sogno, Di Candia, Stefania, Zamproni, Ilaria, Diceglie, Cecilia, Mora,

Journal:

Year:

2013

Language:

english

File:

PDF, 153 KB

english, 2013

99

Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis

Chiereghin, Chiara, Robusto, Michela, Mastrangelo, Antonio, Castorina, Pierangela, Montini, Giovanni, Giani, Marisa, Duga, Stefano, Asselta, Rosanna, Soldà, Giulia, Buratti, Emanuele

Journal:

Year:

2017

Language:

english

File:

PDF, 3.05 MB

english, 2017

100

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes

Paraboschi, Elvezia, Cardamone, Giulia, Rimoldi, Valeria, Gemmati, Donato, Spreafico, Marta, Duga, Stefano, Soldà, Giulia, Asselta, Rosanna

Journal:

International Journal of Molecular Sciences

Year:

2015

Language:

english

File:

PDF, 1.03 MB

english, 2015