224 results on '"Vago, Philippe"'
Search Results
52. ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis
53. A novel 2q14.1q14.3 deletion involvingGLI2andRNU4ATACgenes associated with partial corpus callosum agenesis and severe intrauterine growth retardation
54. Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30‐year French, retrospective, multicentre study
55. Mécanismes moléculaires de la surexpression de hTERT dans le cancer du sein
56. Microdélétion 17q12 et hernie diaphragmatique
57. Exploration cytogénétique des produits de fausse couche spontanée par « Prénatal BoBs™ »
58. Étude de l’organisation spatiale de territoires chromosomiques dans le noyau trisomique 21
59. An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment
60. Prenatal BoBsTM in the cytogenetic analysis of products of spontaneous miscarriage
61. Chapitre 11. Le droit à un enfant chromosomiquement parfait
62. La leucémie myéloïde chronique : du caryotype pour poser le diagnostic au séquençage haut-débit pour la théranostique
63. Prenatal Screening of 21 Microdeletion/Microduplication Syndromes and Subtelomeric Imbalances by MLPA in Fetuses with Increased Nuchal Translucency and Normal Karyotype
64. Fetal skin fibroblasts: A cell model for studying the retinoid pathway in congenital diaphragmatic hernia
65. Congenital diaphragmatic hernia may be associated with 17q12 microdeletion syndrome
66. Abstract 550: Genomic instability and telomere characteristics as predictive biomarkers of therapeutic response in triple-negative breast cancer
67. De novo 2q36.1q36.3 interstitial deletion involving thePAX3andEPHA4genes in a fetus with spina bifida and cleft palate
68. TP53 Disruption and Telomere Instability In Chronic Lymphocytic Leukemia
69. An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3
70. Early Telomere Shortening and Genomic Instability in Tubo-Ovarian Preneoplastic Lesions
71. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation.
72. A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask‐like facial syndrome
73. Laser scanning cytrometry: an alternative technique to study binding site of Bacillus thuringiensis toxins
74. Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities
75. Retinoid Pathway and Congenital Diaphragmatic Hernia: Hypothesis from the Analysis of Chromosomal Abnormalities
76. Trisomy 20q caused by interstitial duplication 20q13.2: Clinical report and literature review
77. Evaluation of Focal Adhesion Kinase Gene Expression in Leukemia and Cancer Cell Lines Using Combined Molecular Cytogenetic Investigations and Quantitative Real Time RT-PCR.
78. Cytogenetic characterization of seven human cancer cell lines by combining G- and R-banding, M-FISH, CGH and chromosome- and locus-specific FISH
79. Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first‐trimester prenatal diagnosis
80. Significance of Molecular Quantification of Minimal Residual Disease in Metastatic Neuroblastoma
81. Potentiel régénératif de l’organe de Corti après ototoxicité
82. De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.
83. An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3.
84. Sequential changes in anti-GAL-1 staining of the rat organ of Corti following amikacin exposure
85. Characterization of atypical cells in the juvenile rat organ of corti after aminoglycoside ototoxicity
86. Attempt at hair cell neodifferentiation in developing and adult amikacin intoxicated rat cochleae
87. Amikacin intoxication induces apoptosis and cell proliferation in rat organ of Corti
88. Identification of preferentially expressed cochlear genes by systematic sequencing of a rat cochlea cDNA library
89. Does the organ of coati attempt to differentiate new hair cells after antibiotic intoxication in rat pups?
90. Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins
91. Structural and ultrastructural aspects of isolated immature cochlear outer hair cells maintained in short-term culture
92. CYTOSKELETAL DEVELOPMENT OF COCHLEAR OUTER HAIR CELLS: A LASER SCANNING IMAGE CYTOMETRIC STUDY
93. OPTIMIZATION OF SPERM PREPARATION INTERNDED FOR IN VITRO FERTILIZATION USING FLOW CYTOMETRY
94. TRISOMY 8 MOSAICISM WITH ATYPICAL PHENOTYPIC FEATURES.
95. FLOW CYTOMETRIC EVALUATION OF CELL PROLIFERATION IN HYPERPARATHYROIDISMS
96. IN VITRO EFFECT OF A MYCOTOXIN: DESTRUXINE E ON HUMAN LEUKEMIC CELLS AND HUMAN LYMPHOCYTES
97. DNA STAINABILITY DEPENDS ON DNA QUANTITY AND DNA ACCESSIBILITY TO DYES
98. Flow cytometric assessment of human spermatozoa
99. Flow cytometry of DNA content as a mean of monitoring cell growth and virus DNA replication in invertebrate cell cultures
100. Laser scanning image cytometric investigation of cochlear outer hair cells during development
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.