20 results on '"Cau, Pierre"'
Search Results
2. Identification of CD146 as a novel molecular actor involved in systemic sclerosis
3. UMD-DYSF, A Novel Locus Specific Database for the Compilation and Interactive Analysis of Mutations in the Dysferlin Gene†
4. High prevalence of laminopathies among patients with metabolic syndrome
5. LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome
6. Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
7. Molecular bases of progeroid syndromes
8. Epilepsy and Deletions at Chromosome 2q24
9. SRPX2 mutations in disorders of language cortex and cognition
10. Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex
11. Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors
12. Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy
13. Complete Loss of the Cytoplasmic Carboxyl Terminus of the KCNQ2 Potassium Channel: A Novel Mutation in a Large Czech Pedigree with Benign Neonatal Convulsions or Other Epileptic Phenotypes
14. Talc for Pleurodesis: Hero or Villain?
15. Lamin A Truncation in Hutchinson-Gilford Progeria
16. Distribution of Calibrated Talc After Intrapleural Administration*: An Experimental Study in Rats
17. Absence of hepatitis C genome in semen of infected men by polymerase chain reaction, branched DNA and in situ hybridization
18. Early Detection of Airway Involvement in Obliterative Bronchiolitis after Lung Transplantation: Functional and Bronchoalveolar Lavage Cell Findings
19. HUMAN MESOTHELIOMA. CYTOLOGICAL AND IMMUNOCYTOCHEMICAL DIAGNOSIS IN PLEURAL EFFUSIONS. TRANSMISSION, SCANNING ELECTRON MICROSCOPY AND X-RAY MICROANALYSIS OF ISOLATED CELLS AND OF PARIETAL HUMAN PLEURA
20. NHE-3 isoform of the Na+/H+ exchanger in human gallbladder: Localization of specific mRNA by in situ hybridization
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