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-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 situs abnormalities result from mutations in ZIC3
1997-01-01 Gebbia M; Ferrero GB; Pilia G; Bassi MT; Aylsworth A; Penman-Splitt M; Bird LM; Bamforth JS; Burn J; Schlessinger D; Nelson DL; Casey B.
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene
1995-01-01 VILLA A; NOTARANGELO L; MACCHI P; MANTUANO E; CAVAGNI G; BRUGNONI D; STRINA D; PATROSSO MC; U. RAMENGHI; SACCO MG; UGAZIO AG
X-Ray Absorption and Emission Spectroscopy for Catalysis
2016-01-01 Lamberti, Carlo; van Bokhoven, Jeroen A.
| 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-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 situs abnormalities result from mutations in ZIC3 | 1997 | Gebbia M; Ferrero GB; Pilia G; Bassi MT; Aylsworth A; Penman-Splitt M; Bird LM; Bamforth JS; Burn J; Schlessinger D; Nelson DL; Casey B. | |
| X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene | 1995 | VILLA A; NOTARANGELO L; MACCHI P; MANTUANO E; CAVAGNI G; BRUGNONI D; STRINA D; PATROSSO MC; U. RAMENGHI; SACCO MG; UGAZIO AG | |
| X-Ray Absorption and Emission Spectroscopy for Catalysis | 2016 | Lamberti, Carlo; van Bokhoven, Jeroen A. |
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