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336 results on '"Ciccodicola, Alfredo"'

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51. RBPMetaDB: a comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins.

52. Complex events in the evolution of the human pseudoautosomal region 2(PAR2)

53. Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

55. Antigen delivery by filamentous bacteriophage fd displaying an anti‐ DEC ‐205 single‐chain variable fragment confers adjuvanticity by triggering a TLR 9‐mediated immune response

59. Uncovering the Complexity of Transcriptomes with RNA-Seq

60. PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues

61. SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets.

64. Investigation of gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility

67. Evidence of Bacteroides fragilis Protection from Bartonella henselae-Induced Damage

70. Massive-scale RNA-Seq experiments in human genetic diseases

73. Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21

74. Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients

75. Screening forGJB2andGJB6gene mutations in patients from Campania region with sensorineural hearing loss

79. Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

80. Experimental colitis: decreased Octn2 and Atb0+ expression in rat colonocytes induces carnitine depletion that is reversible by carnitine‐loaded liposomes

81. A Novel Peroxisome Proliferator-activated Receptor γ Isoform with Dominant Negative Activity Generated by Alternative Splicing

82. Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

85. Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

86. Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains

88. Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site

89. Human homologue of the murinebare patches/striated gene is not mutated in incontinentia pigmenti type 2

90. Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2

91. Human and mouse SYBL1 gene structure and expression

92. Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa

97. Expressed STSs and transcription of human Xq28

99. SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function

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