266 results on '"Fanen P"'
Search Results
2. Novel Green Method for Synthesizing Plane Tree Seeds-Based Porous Carbon Used as Symmetric Supercapacitors
3. Highly Porous Carbon Materials Based on Cicada Slough for Outstanding Supercapacitor Performance
4. Assessing the role of participatory planning approach in enhancing informal settlements upgrading in low income regions
5. Threonine fuels glioblastoma through YRDC-mediated codon-biased translational reprogramming
6. N–self–doped hierarchically porous carbon materials from waste coffee grounds for symmetric supercapacitor
7. Lysine catabolism reprograms tumour immunity through histone crotonylation
8. Identification and validation of a novel prognostic signature based on mitochondria and oxidative stress related genes for glioblastoma
9. Les amyloses cardiaques : état des lieux en 2022
10. The dual role of p62 in ferroptosis of glioblastoma according to p53 status
11. HSP27 protects against ferroptosis of glioblastoma cells
12. Surfactant protein B deficiency: the RespiRare cohort
13. Use of circulating tumor cells and microemboli to predict diagnosis and prognosis in diffuse glioma.
14. TGF-β induces GBM mesenchymal transition through upregulation of CLDN4 and nuclear translocation to activate TNF-α/NF-κB signal pathway
15. Extracardiac soft tissue uptake, evidenced on early 99mTc-HMDP SPECT/CT, helps typing cardiac amyloidosis and demonstrates high prognostic value
16. mTORC1 activity regulates post-translational modifications of glycine decarboxylase to modulate glycine metabolism and tumorigenesis
17. Amylo-AFFECT-QOL, a self-reported questionnaire to assess health-related quality of life and to determine the prognosis in cardiac amyloidosis
18. Corrélations phénotype-génotype des patients pédiatriques porteurs de mutations bi-alléliques du gène lié au surfactant ABCA3
19. Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosis
20. Real-life evaluation of an algorithm for the diagnosis of cardiac amyloidosis
21. Prévalence du cancer du poumon dans une cohorte de patients porteurs d’une mutation d’un gène lié au surfactant
22. Homozygote and heterozygote transthyretin p.Val142Ile (V122I) genetic variant: Comparison of cardiac involvement, extracardiac manifestations and outcomes
23. The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy
24. Changes in amyloidosis phenotype over 11 years in a cardiac amyloidosis referral centre cohort in France.
25. Identification of glioblastoma gene prognosis modules based on weighted gene co-expression network analysis
26. Vulnerability and adaptation of rice value chains in Benue State, Nigeria
27. Single Remote Sensing Image Super-Resolution via a Generative Adversarial Network With Stratified Dense Sampling and Chain Training
28. A Downscaling Framework for Urban Nighttime Light Based on Multifactor Geographically Neural Network Weighted Regression
29. High Prevalence and impact of lung cancer in Surfactant related gene mutation carriers
30. Pathologies respiratoires de l’enfant associées à des anomalies héréditaires du métabolisme du surfactant
31. Pathologies génétiques du surfactant
32. P013 Peptide modulation of COMMD1: corrector and anti-inflammatory effect in cystic fibrosis context?
33. The Impact of Air Pollution on the Course of Cystic Fibrosis: A Review. Front. Physiol
34. Prevalence and determinant of iron deficiency in the three main types of cardiac amyloidosis
35. Pathologie du surfactant : diagnostic, présentation initiale, évolution et prise en charge des enfants porteurs d’une mutation SFTPC
36. A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotype
37. Natural history and impact of treatment with tafamidis on major cardiovascular outcome-free survival time in a cohort of patients with transthyretin amyloidosis
38. Prevalence and type of first amyloid extracardiac symptoms and cardiac disorders history and time from their occurrence to diagnosis between Al and transthyretin cardiac amyloidosis
39. WS21.3 Overview of shared benefits from the 6-year long collaboration between the French Cystic Fibrosis Registry and the CFTR-France genetics database
40. S05.4 HspB5 is a phospho-regulated corrector of F508del-CFTR
41. Dose-response effect of serum butyrylcholinesterase activity after clinical doses of pancuronium
42. IDENTIFICATION OF CFTR EXONIC SEQUENCE VARIATIONS AFFECTING EXON 3, 4 AND 5 SPLICING: 228
43. Three point mutations in the CFTR gene in French cystic fibrosis patients: Identification by denaturing gradient gel electrophoresis
44. CFTRgene variants: a predisposition factor to aquagenic palmoplantar keratoderma
45. P017 Update of CFTR-France: toward a more relevant dataset for predicting the impact of rare CFTR variants
46. P019 Variants in the CFTR gene: a predisposition factor to aquagenic palmoplantar keratoderma
47. Études structure-fonction de mutants d’ABCA3 dans le cadre de pathologie héréditaire du surfactant pulmonaire
48. Le syndrome 48, XXYY : une nouvelle étiologie génétique d’hyperplasie neuroendocrine du nourrisson
49. Study of congenital heart defects among neonates in Jos, Nigeria: prevalence and spectrum.
50. Short-term outcomes and predictors of post-surgical seizures in patients with supratentorial low-grade gliomas.
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