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2. Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia

3. Activation of the Human Homologue of the Drosophila sina Gene in Apoptosis and Tumor Suppression

8. Additional file 4: Table S4. of Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A

10. Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43

13. Continuum of overlapping clones spanning the entire human chromosome 21q

14. Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene

15. Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A

16. Combination of acamprosate and baclofen as a promising therapeutic approach for Parkinson’s disease

17. A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment

18. Combining two repurposed drugs as a promising approach for Alzheimer's disease therapy

19. An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A

20. Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 over-expression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy

21. Reading the Evolutionary History of the Woolly Mammoth in Its Mitochondrial Genome

22. A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer’s Disease.

23. Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 overexpression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy.

29. Structure and Physical Mapping of DR1, a TATA-Binding Protein-Associated Phosphoprotein Gene, to Chromosome 1p22.1 and Its Exclusion in Stargardt Disease (STGD)

31. A 1.6-Mb P1-Based Physical Map of the Down Syndrome Region on Chromosome 21

33. High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)

34. Cosmid assembly and anchoring to human chromosome 21

35. A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening

37. Cloning the Human Major Histocompatibility Complex in YACs

38. Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy

40. Mapping the whole human genome by fingerprinting yeast artificial chromosomes

41. Complete Mitochondrial Genome and Phylogeny of Pleistocene Mammoth Mammuthus primigenius.

42. A YAC contig map of the human genome.

44. Survey of CAG/CTG Repeats in Human cDNAs Representing New Genes: Candidates for Inherited Neurological Disorders.

46. Cloning of Two Genetically Transmitted Moloney Leukemia Proviral Genomes: Correlation Between Biological Activity of the Cloned DNA and Viral Genome Activation in the Animal

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