61 results on '"A, Lombès"'
Search Results
2. Homoplasmic mitochondrial tRNAPro mutation causing exercise-induced muscle swelling and fatigue
3. Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome
4. Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation
5. Human diseases caused by mitochondrial DNA mutations: from diagnosis to pathophysiology: 5.12
6. Prevalence of cardiac involvement in mitochondrial diseases: 2.34
7. Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases
8. Aldosterone-Signaling Defect Exacerbates Sodium Wasting in Very Preterm Neonates: The Premaldo Study
9. Lipoprotein-Free Mitotane Exerts High Cytotoxic Activity in Adrenocortical Carcinoma
10. A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity
11. Salsalate Activates Brown Adipose Tissue in Mice
12. The neuronal mineralocorticoid receptor: From cell survival to neurogenesis
13. Switch in FGFR3 and -4 Expression Profile During Human Renal Development May Account for Transient Hypercalcemia in Patients With Sotos Syndrome due to 5q35 Microdeletions
14. Growth Hormone, Insulin-Like Growth Factor-1, and the Kidney: Pathophysiological and Clinical Implications
15. Metformin Lowers Plasma Triglycerides by Promoting VLDL-Triglyceride Clearance by Brown Adipose Tissue in Mice
16. Hibernoma: A Clinical Model for Exploring the Role of Brown Adipose Tissue in the Regulation of Body Weight?
17. Probenecid potentiates MPTP/MPP+ toxicity by interference with cellular energy metabolism
18. Molecular Screening for a Personalized Treatment Approach in Advanced Adrenocortical Cancer
19. A New Strategy for Selective Targeting of Progesterone Receptor With Passive Antagonists
20. NR5A1 (SF-1) Mutations Are Not a Major Cause of Primary Ovarian Insufficiency
21. Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome
22. What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?
23. Pathophysiology of Renal Calcium Handling in Acromegaly: What Lies behind Hypercalciuria?
24. Mineralocorticoid Receptor Overexpression Facilitates Differentiation and Promotes Survival of Embryonic Stem Cell-Derived Neurons
25. p38 and p42/44 MAPKs Differentially Regulate Progesterone Receptor A and B Isoform Stabilization
26. Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria
27. Body Fluid Expansion in Acromegaly Is Related to Enhanced Epithelial Sodium Channel (ENaC) Activity
28. Aldosterone Postnatally, but not at Birth, Is Required for Optimal Induction of Renal Mineralocorticoid Receptor Expression and Sodium Reabsorption
29. Ligand-Dependent Degradation of SRC-1 Is Pivotal for Progesterone Receptor Transcriptional Activity
30. Mineralocorticoid receptor overexpression in embryonic stem cell-derived cardiomyocytes increases their beating frequency
31. Regulation of Mineralocorticoid Receptor Expression during Neuronal Differentiation of Murine Embryonic Stem Cells
32. Osmotic Stress Regulates Mineralocorticoid Receptor Expression in a Novel Aldosterone-Sensitive Cortical Collecting Duct Cell Line
33. Natural lipophilic inhibitors of mitochondrial complex I are candidate toxins for sporadic neurodegenerative tau pathologies
34. Low Renal Mineralocorticoid Receptor Expression at Birth Contributes to Partial Aldosterone Resistance in Neonates
35. Isolated Familial Hypogonadotropic Hypogonadism and a GNRH1 Mutation
36. Lack of Androgen Receptor Expression in Sertoli Cells Accounts for the Absence of Anti-Mullerian Hormone Repression during Early Human Testis Development
37. Liver damage underlying unexplained transaminase elevation in human immunodeficiency virus-1 mono-infected patients on antiretroviral therapy#
38. Epithelial Sodium Channel Is a Key Mediator of Growth Hormone-Induced Sodium Retention in Acromegaly
39. Human fetal testis: source of estrogen and target of estrogen action
40. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?
41. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
42. Ligand-Controlled Interaction of Histone Acetyltransferase Binding to ORC-1 (HBO1) with the N-Terminal Transactivating Domain of Progesterone Receptor Induces Steroid Receptor Coactivator 1-Dependent Coactivation of Transcription
43. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation
44. The Mineralocorticoid Receptor: A Journey Exploring Its Diversity and Specificity of Action
45. FoxO3 Mediates Antagonistic Effects of Glucocorticoids and Interleukin-2 on Glucocorticoid-Induced Leucine Zipper Expression
46. The Elongation Factor ELL (Eleven-Nineteen Lysine-Rich Leukemia) Is a Selective Coregulator for Steroid Receptor Functions
47. Adult-onset chorea and mitochondrial cytopathy
48. The HIV-1 nucleoside reverse transcriptase inhibitors stavudine and zidovudine alter adipocyte functions in vitro
49. New Naturally Occurring Missense Mutations of the Human Mineralocorticoid Receptor Disclose Important Residues Involved in Dynamic Interactions with Deoxyribonucleic Acid, Intracellular Trafficking, and Ligand Binding
50. Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.