Sfoglia per Titolo
X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells
2018-01-01 Ho, Bianca; Greenlaw, Keelin; Al Tuwaijri, Abeer; Moussette, Sanny; Martínez, Francisco; Giorgio, Elisa; Brusco, Alfredo; Ferrero, Giovanni Battista; Linhares, Natália D; Valadares, Eugênia R; Svartman, Marta; Kalscheuer, Vera M; Rodríguez Criado, Germán; Laprise, Catherine; Greenwood, Celia M T; Naumova, Anna K
X Cittadino
2010-01-01 Ljiljana Banjanin
X Congresso della FIEC (Québec, 23-27 Agosto 1994)
1995-01-01 E. MALASPINA
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred
1996-01-01 MacKenzie JJ; Fitzpatrick J; Babyn P; Ferrero GB; Ballabio A; Billingsley G; Bulman DE; Strasberg P; Ray PN; Costa T.
X-chromosome in Italy: A database of 29 STR markers
2011-01-01 Presciuttini S; Toni C; Alù M; Asmundo A; Baldassarri L; Barbaro A; Caenazzo L; Carnevali E; Cerri N; D’Aloia E; Di Nunzio C; Onofri V; Peloso G; Pelotti S; Piccinini A; Robino C; Turrina S; Venturi M; Domenici R
X-chromosome-wide association study for Alzheimer's disease
2024-01-01 Le Borgne, Julie; Gomez, Lissette; Heikkinen, Sami; Amin, Najaf; Ahmad, Shahzad; Choi, Seung Hoan; Bis, Joshua; Grenier-Boley, Benjamin; Rodriguez, Omar Garcia; Kleineidam, Luca; Young, Juan; Tripathi, Kumar Parijat; Wang, Lily; Varma, Achintya; Campos-Martin, Rafael; van der Lee, Sven; Damotte, Vincent; de Rojas, Itziar; Palmal, Sagnik; EADB, Rubino Elisa, GR@ACE, DEGESCO, EADI, GERAD, DemGene, FinnGen, ADGC, CHARGE; Lipton, Richard; Reiman, Eric; McKee, Ann; De Jager, Philip; Bush, William; Small, Scott; Levey, Allan; Saykin, Andrew; Foroud, Tatiana; Albert, Marilyn; Hyman, Bradley; Petersen, Ronald; Younkin, Steven; Sano, Mary; Wisniewski, Thomas; Vassar, Robert; Schneider, Julie; Henderson, Victor; Roberson, Erik; DeCarli, Charles; LaFerla, Frank; Brewer, James; Swerdlow, Russell; Van Eldik, Linda; Hamilton-Nelson, Kara; Paulson, Henry; Naj, Adam; Lopez, Oscar; Chui, Helena; Crane, Paul; Grabowski, Thomas; Kukull, Walter; Asthana, Sanjay; Craft, Suzanne; Strittmatter, Stephen; Cruchaga, Carlos; Leverenz, James; Goate, Alison; Kamboh, M Ilyas; George-Hyslop, Peter St; Valladares, Otto; Kuzma, Amanda; Cantwell, Laura; Riemenschneider, Matthias; Morris, John; Slifer, Susan; Dalmasso, Carolina; Castillo, Atahualpa; Küçükali, Fahri; Peters, Oliver; Schneider, Anja; Dichgans, Martin; Rujescu, Dan; Scherbaum, Norbert; Deckert, Jürgen; Riedel-Heller, Steffi; Hausner, Lucrezia; Molina-Porcel, Laura; Düzel, Emrah; Grimmer, Timo; Wiltfang, Jens; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Tegos, Thomas; Scarmeas, Nikolaos; Dols-Icardo, Oriol; Moreno, Fermin; Pérez-Tur, Jordi; Bullido, María J; Pastor, Pau; Sánchez-Valle, Raquel; Álvarez, Victoria; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Mir, Pablo; Real, Luis M; Piñol-Ripoll, Gerard; García-Alberca, Jose María; Royo, Jose Luís; Rodriguez-Rodriguez, Eloy; Soininen, Hilkka; de Mendonça, Alexandre; Mehrabian, Shima; Traykov, Latchezar; Hort, Jakub; Vyhnalek, Martin; Thomassen, Jesper Qvist; Pijnenburg, Yolande A L; Holstege, Henne; van Swieten, John; Ramakers, Inez; Verhey, Frans; Scheltens, Philip; Graff, Caroline; Papenberg, Goran; Giedraitis, Vilmantas; Boland, Anne; Deleuze, Jean-François; Nicolas, Gael; Dufouil, Carole; Pasquier, Florence; Hanon, Olivier; Debette, Stéphanie; Grünblatt, Edna; Popp, Julius; Ghidoni, Roberta; Galimberti, Daniela; Arosio, Beatrice; Mecocci, Patrizia; Solfrizzi, Vincenzo; Parnetti, Lucilla; Squassina, Alessio; Tremolizzo, Lucio; Borroni, Barbara; Nacmias, Benedetta; Spallazzi, Marco; Seripa, Davide; Rainero, Innocenzo; Daniele, Antonio; Bossù, Paola; Masullo, Carlo; Rossi, Giacomina; Jessen, Frank; Fernandez, Victoria; Kehoe, Patrick Gavin; Frikke-Schmidt, Ruth; Tsolaki, Magda; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Haines, Jonathan; Farrer, Lindsay; Mayeux, Richard; Wang, Li-San; Sims, Rebecca; DeStefano, Anita; Schellenberg, Gerard D; Seshadri, Sudha; Amouyel, Philippe; Williams, Julie; van der Flier, Wiesje; Ramirez, Alfredo; Pericak-Vance, Margaret; Andreassen, Ole A; Van Duijn, Cornelia; Hiltunen, Mikko; Ruiz, Agustín; Dupuis, Josée; Martin, Eden; Lambert, Jean-Charles; Kunkle, Brian; Bellenguez, Céline
X-CT Reconstruction as a Tool for Monitoring the Conservation State and Decay Processes of Works of Art and in Support of Restoration and Conservation Strategies
2025-01-01 Guidorzi, Laura; Re, Alessandro; Tansella, Francesca; Vigorelli, Luisa; Ricci, Chiara; Ryan, Joseph; Lo Giudice, Alessandro
X-Hinter
2011-01-01 A. Panisson; R. Schifanella; G. Ruffo
X-hinter: a framework for implementing social oriented recommender systems
2008-01-01 A. Panisson; G. Ruffo; R. Schifanella
X-Klaim and Klava: Programming Mobile Code
2002-01-01 Lorenzo Bettini;Rocco De Nicola;Rosario Pugliese
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
1996-01-01 RENIERI A ;BRUTTINI M ;GALLI L ;ZANELLI P ;NERI T ;ROSSETTI S ;TURCO A ;HEISKARI N ;ZHOU J ;GUSMANO R ;MASSELLA L ;BANFI G ;SCOLARI F ;SESSA A ;RIZZONI G ;TRYGGVASON K ;PIGNATTI PF ;SAVI M ;BALLABIO A ;DE MARCHI M
X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study
2003-01-01 JAIS JP; KNEBELMANN B; GIATRAS I; M. DE MARCHI; RIZZONI GF; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; DAHAN K; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ PM; SCHRDER C; SANAK M; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H AND GUBLER MC
X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.
2000-01-01 JAIS JP; KNEBELMANN B; GIATRAS I; DE MARCHI M; RIZZONI G; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; VERELLEN C; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ JM; SCHRÖDER C; SANAK M; KREJCOVA S; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H; GUBLER MC
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families.
2003-01-01 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.
[X-linked congenital hydrocephalus. Description of a case]
1978-01-01 SPADA A ;DE MARCHI M ;MELLANO G
X-linked ectodermal dysplasia. Presentation of 2 cases.
1984-01-01 Landi M; Ricca V; Oggero R; Guardamagna O; Cortelazzo MV; Sandrucci M.
X-Linked Hereditary Nephropathy in Navasota Dogs: Clinical Pathology, Morphology, and Gene Expression During Disease Progression
2016-01-01 Benali S.L; Lees G.E.; Nabity M.B.; Aricò A.; Drigo M.; Gallo E.; Giantin M.; Aresu L.
X-linked hypophosphatemic rickets: An Italian experts' opinion survey
2019-01-01 Emma F.; Cappa M.; Antoniazzi F.; Bianchi M.L.; Chiodini I.; Eller Vainicher C.; Di Iorgi N.; Maghnie M.; Cassio A.; Balsamo A.; Baronio F.; De Sanctis L.; Tessaris D.; Baroncelli G.I.; Mora S.; Brandi M.L.; Weber G.; D'Ausilio A.; Lanati E.P.
X-Linked Immunodeficient Mice With No Functional Bruton's Tyrosine Kinase Are Protected From Sepsis-Induced Multiple Organ Failure
2020-01-01 O'Riordan C.E.; Purvis G.S.D.; Collotta D.; Krieg N.; Wissuwa B.; Sheikh M.H.; Ferreira Alves G.; Mohammad S.; Callender L.A.; Coldewey S.M.; Collino M.; Greaves D.R.; Thiemermann C.
X-linked sideroblastic anaemia associated with beta thalassemia trait presenting with a peculiar chronic anaemia phenotype in a 47-years-old woman
2025-01-01 Francesco Pintus, Noemi Giordano, Carmen Maria Gaglioti, Irene Motta, Alfredo Brusco, Daniela Francesca Giachino, G.B. Ferrero, Giorgia Mandrile
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells | 2018 | Ho, Bianca; Greenlaw, Keelin; Al Tuwaijri, Abeer; Moussette, Sanny; Martínez, Francisco; Giorgio, Elisa; Brusco, Alfredo; Ferrero, Giovanni Battista; Linhares, Natália D; Valadares, Eugênia R; Svartman, Marta; Kalscheuer, Vera M; Rodríguez Criado, Germán; Laprise, Catherine; Greenwood, Celia M T; Naumova, Anna K | |
| X Cittadino | 2010 | Ljiljana Banjanin | |
| X Congresso della FIEC (Québec, 23-27 Agosto 1994) | 1995 | E. MALASPINA | |
| X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred | 1996 | MacKenzie JJ; Fitzpatrick J; Babyn P; Ferrero GB; Ballabio A; Billingsley G; Bulman DE; Strasberg P; Ray PN; Costa T. | |
| X-chromosome in Italy: A database of 29 STR markers | 2011 | Presciuttini S; Toni C; Alù M; Asmundo A; Baldassarri L; Barbaro A; Caenazzo L; Carnevali E; Cerri N; D’Aloia E; Di Nunzio C; Onofri V; Peloso G; Pelotti S; Piccinini A; Robino C; Turrina S; Venturi M; Domenici R | |
| X-chromosome-wide association study for Alzheimer's disease | 2024 | Le Borgne, Julie; Gomez, Lissette; Heikkinen, Sami; Amin, Najaf; Ahmad, Shahzad; Choi, Seung Hoan; Bis, Joshua; Grenier-Boley, Benjamin; Rodriguez, Omar Garcia; Kleineidam, Luca; Young, Juan; Tripathi, Kumar Parijat; Wang, Lily; Varma, Achintya; Campos-Martin, Rafael; van der Lee, Sven; Damotte, Vincent; de Rojas, Itziar; Palmal, Sagnik; EADB, Rubino Elisa, GR@ACE, DEGESCO, EADI, GERAD, DemGene, FinnGen, ADGC, CHARGE; Lipton, Richard; Reiman, Eric; McKee, Ann; De Jager, Philip; Bush, William; Small, Scott; Levey, Allan; Saykin, Andrew; Foroud, Tatiana; Albert, Marilyn; Hyman, Bradley; Petersen, Ronald; Younkin, Steven; Sano, Mary; Wisniewski, Thomas; Vassar, Robert; Schneider, Julie; Henderson, Victor; Roberson, Erik; DeCarli, Charles; LaFerla, Frank; Brewer, James; Swerdlow, Russell; Van Eldik, Linda; Hamilton-Nelson, Kara; Paulson, Henry; Naj, Adam; Lopez, Oscar; Chui, Helena; Crane, Paul; Grabowski, Thomas; Kukull, Walter; Asthana, Sanjay; Craft, Suzanne; Strittmatter, Stephen; Cruchaga, Carlos; Leverenz, James; Goate, Alison; Kamboh, M Ilyas; George-Hyslop, Peter St; Valladares, Otto; Kuzma, Amanda; Cantwell, Laura; Riemenschneider, Matthias; Morris, John; Slifer, Susan; Dalmasso, Carolina; Castillo, Atahualpa; Küçükali, Fahri; Peters, Oliver; Schneider, Anja; Dichgans, Martin; Rujescu, Dan; Scherbaum, Norbert; Deckert, Jürgen; Riedel-Heller, Steffi; Hausner, Lucrezia; Molina-Porcel, Laura; Düzel, Emrah; Grimmer, Timo; Wiltfang, Jens; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Tegos, Thomas; Scarmeas, Nikolaos; Dols-Icardo, Oriol; Moreno, Fermin; Pérez-Tur, Jordi; Bullido, María J; Pastor, Pau; Sánchez-Valle, Raquel; Álvarez, Victoria; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Mir, Pablo; Real, Luis M; Piñol-Ripoll, Gerard; García-Alberca, Jose María; Royo, Jose Luís; Rodriguez-Rodriguez, Eloy; Soininen, Hilkka; de Mendonça, Alexandre; Mehrabian, Shima; Traykov, Latchezar; Hort, Jakub; Vyhnalek, Martin; Thomassen, Jesper Qvist; Pijnenburg, Yolande A L; Holstege, Henne; van Swieten, John; Ramakers, Inez; Verhey, Frans; Scheltens, Philip; Graff, Caroline; Papenberg, Goran; Giedraitis, Vilmantas; Boland, Anne; Deleuze, Jean-François; Nicolas, Gael; Dufouil, Carole; Pasquier, Florence; Hanon, Olivier; Debette, Stéphanie; Grünblatt, Edna; Popp, Julius; Ghidoni, Roberta; Galimberti, Daniela; Arosio, Beatrice; Mecocci, Patrizia; Solfrizzi, Vincenzo; Parnetti, Lucilla; Squassina, Alessio; Tremolizzo, Lucio; Borroni, Barbara; Nacmias, Benedetta; Spallazzi, Marco; Seripa, Davide; Rainero, Innocenzo; Daniele, Antonio; Bossù, Paola; Masullo, Carlo; Rossi, Giacomina; Jessen, Frank; Fernandez, Victoria; Kehoe, Patrick Gavin; Frikke-Schmidt, Ruth; Tsolaki, Magda; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Haines, Jonathan; Farrer, Lindsay; Mayeux, Richard; Wang, Li-San; Sims, Rebecca; DeStefano, Anita; Schellenberg, Gerard D; Seshadri, Sudha; Amouyel, Philippe; Williams, Julie; van der Flier, Wiesje; Ramirez, Alfredo; Pericak-Vance, Margaret; Andreassen, Ole A; Van Duijn, Cornelia; Hiltunen, Mikko; Ruiz, Agustín; Dupuis, Josée; Martin, Eden; Lambert, Jean-Charles; Kunkle, Brian; Bellenguez, Céline | |
| X-CT Reconstruction as a Tool for Monitoring the Conservation State and Decay Processes of Works of Art and in Support of Restoration and Conservation Strategies | 2025 | Guidorzi, Laura; Re, Alessandro; Tansella, Francesca; Vigorelli, Luisa; Ricci, Chiara; Ryan, Joseph; Lo Giudice, Alessandro | |
| X-Hinter | 2011 | A. Panisson; R. Schifanella; G. Ruffo | |
| X-hinter: a framework for implementing social oriented recommender systems | 2008 | A. Panisson; G. Ruffo; R. Schifanella | |
| X-Klaim and Klava: Programming Mobile Code | 2002 | Lorenzo Bettini;Rocco De Nicola;Rosario Pugliese | |
| X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. | 1996 | RENIERI A ;BRUTTINI M ;GALLI L ;ZANELLI P ;NERI T ;ROSSETTI S ;TURCO A ;HEISKARI N ;ZHOU J ;GUSMANO R ;MASSELLA L ;BANFI G ;SCOLARI F ;SESSA A ;RIZZONI G ;TRYGGVASON K ;PIGNATTI PF ;SAVI M ;BALLABIO A ;DE MARCHI M | |
| X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study | 2003 | JAIS JP; KNEBELMANN B; GIATRAS I; M. DE MARCHI; RIZZONI GF; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; DAHAN K; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ PM; SCHRDER C; SANAK M; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H AND GUBLER MC | |
| X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males. | 2000 | JAIS JP; KNEBELMANN B; GIATRAS I; DE MARCHI M; RIZZONI G; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; VERELLEN C; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ JM; SCHRÖDER C; SANAK M; KREJCOVA S; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H; GUBLER MC | |
| X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families. | 2003 | Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L. | |
| [X-linked congenital hydrocephalus. Description of a case] | 1978 | SPADA A ;DE MARCHI M ;MELLANO G | |
| X-linked ectodermal dysplasia. Presentation of 2 cases. | 1984 | Landi M; Ricca V; Oggero R; Guardamagna O; Cortelazzo MV; Sandrucci M. | |
| X-Linked Hereditary Nephropathy in Navasota Dogs: Clinical Pathology, Morphology, and Gene Expression During Disease Progression | 2016 | Benali S.L; Lees G.E.; Nabity M.B.; Aricò A.; Drigo M.; Gallo E.; Giantin M.; Aresu L. | |
| X-linked hypophosphatemic rickets: An Italian experts' opinion survey | 2019 | Emma F.; Cappa M.; Antoniazzi F.; Bianchi M.L.; Chiodini I.; Eller Vainicher C.; Di Iorgi N.; Maghnie M.; Cassio A.; Balsamo A.; Baronio F.; De Sanctis L.; Tessaris D.; Baroncelli G.I.; Mora S.; Brandi M.L.; Weber G.; D'Ausilio A.; Lanati E.P. | |
| X-Linked Immunodeficient Mice With No Functional Bruton's Tyrosine Kinase Are Protected From Sepsis-Induced Multiple Organ Failure | 2020 | O'Riordan C.E.; Purvis G.S.D.; Collotta D.; Krieg N.; Wissuwa B.; Sheikh M.H.; Ferreira Alves G.; Mohammad S.; Callender L.A.; Coldewey S.M.; Collino M.; Greaves D.R.; Thiemermann C. | |
| X-linked sideroblastic anaemia associated with beta thalassemia trait presenting with a peculiar chronic anaemia phenotype in a 47-years-old woman | 2025 | Francesco Pintus, Noemi Giordano, Carmen Maria Gaglioti, Irene Motta, Alfredo Brusco, Daniela Francesca Giachino, G.B. Ferrero, Giorgia Mandrile |
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