193 results on '"Saudek, Vladimir"'
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2. Obesity-associated gene TMEM18 has a role in the central control of appetite and body weight regulation
3. Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy
4. BIR-1, a Caenorhabditis elegans Homologue of Survivin, Regulates Transcription and Development
5. SKIP is an Indispensable Factor for Caenorhabditis elegans Development
6. FTO is necessary for the induction of leptin resistance by high-fat feeding
7. Perilipins 2 and 3 lack a carboxy-terminal domain present in perilipin 1 involved in sequestering ABHD5 and suppressing basal lipolysis
8. Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease
9. Endoplasmic reticulum stress-induced transcription factor, CHOP, is crucial for dendritic cell IL-23 expression
10. The Direct Determination of Protein Structure from Multidimensional NMR Spectra without Assignment : An Evaluation of the Concept
11. The Obesity-Associated FTO Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase
12. Correction: Conserved amphipathic helices mediate lipid droplet targeting of perilipins 1–3
13. Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution
14. Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance
15. Identification of rare loss of function variation regulating body fat distribution
16. Clinical and Molecular Characterization of a Novel PLIN1 Frameshift Mutation Identified in Patients With Familial Partial Lipodystrophy
17. Correlation between biochemical findings, structural and enzymatic abnormalities in mutated HMBS identified in six Israeli families with acute intermittent porphyria
18. Phenotypic characterization of Adig null mice suggests roles for adipogenin in the regulation of fat mass accrual and leptin secretion
19. Structure activity relationship by NMR and by computer: a comparative study
20. GDF15: A Hormone Conveying Somatic Distress to the Brain
21. Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals
22. Partial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in CIDEC
23. Acute intermittent porphyria – impact of mutations found in the hydroxymethylbilane synthase gene on biochemical and enzymatic protein properties
24. Dual binding motifs underpin the hierarchical association of perilipins1–3 with lipid droplets
25. Gradient-tailored excitation for single-quantum NMR spectroscopy of aqueous solutions
26. Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution
27. PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress
28. Conformational studies of the RGD containing peptide echistatin
29. The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
30. Genome-wide scan and fine-mapping of rare nonsynonymous associations implicates intracellular lipolysis genes in fat distribution and cardio-metabolic risk
31. PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress
32. Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
33. Conserved Amphipathic Helices Mediate Lipid Droplet Targeting of Perilipins 1–3
34. Potential dual function of PQ-loop proteins such as cystinosin
35. Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
36. Loss and gain of function experiments implicate TMEM18 as a mediator of the strong association between genetic variants at human Chromosome 2p25.3 and obesity
37. Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
38. FICD acts bifunctionally to AMPylate and de-AMPylate the endoplasmic reticulum chaperone BiP
39. The human lipodystrophy protein seipin is an ER membrane adaptor for the adipogenic PA phosphatase lipin 1
40. FICD acts bi-functionally to AMPylate and de-AMPylate the endoplasmic reticulum chaperone BiP
41. Lichen sclerosus et atrophicus-like skin lesions in a patient carrying a novel hydroxymethylbilane synthase mutation
42. Clinical and Molecular Characterization of a Novel PLIN1 Frameshift Mutation Identified in Patients With Familial Partial Lipodystrophy
43. Cystinosin, MPDU1, SWEETs and KDELR Belong to a Well-Defined Protein Family with Putative Function of Cargo Receptors Involved in Vesicle Trafficking
44. FICD acts bifunctionally to AMPylate and de-AMPylate the endoplasmic reticulum chaperone BiP
45. Human Frame Shift Mutations Affecting the Carboxyl Terminus of Perilipin Increase Lipolysis by Failing to Sequester the Adipose Triglyceride Lipase (ATGL) Coactivator AB-hydrolase-containing 5 (ABHD5)
46. Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals
47. Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations
48. Solution conformation of Endothelin-1 by 1H NMR, CD, and molecular modeling
49. The Obesity-AssociatedFTOGene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase
50. Sequence Identification and Characterization of Human Carnosinase and a Closely Related Non-specific Dipeptidase
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