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3. G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy

4. Label-free quantitative proteomics and SAINT analysis enable interactome mapping for the human Ser/Thr protein phosphatase 5

5. Influence of hormones and hormone metabolites on the growth of schwann cells derived from embryonic stem cells and on tumor cell lines expressing variable levels of neurofibromin This article was accepted for inclusion in the Special Focus on Stem Cells??? Developmental Dynamics 236 #12 .

6. Tumor necrosis factor–Α contributes to below-level neuropathic pain after spinal cord injury

7. Identification of genes within the Krd deletion on mouse Chromosome 19

8. Gene transfer of glutamic acid decarboxylase reduces neuropathic pain

9. Increased Cell-Substrate Adhesion Accompanies Conditional Reversion to the Normal Phenotype in Ras-Oncogene-Transformed NIH-3T3 Cells

10. Smooth Muscle Myosin Heavy Chain Locus (MYH11) Maps to 16p13.13-p13.12 and Establishes a New Region of Conserved Synteny between Human 16p and Mouse 16

11. Molecular Genetics of Lactase Deficiencies

12. Fullerene and ruthenium dual end-functionalized thermosensitive polymers: synthesis, characterization, electrochemical properties, and self-assemblyElectronic supplementary information (ESI) available: Additional figures; experimental methods. See DOI: 10.1039/b805449e

14. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

15. Guidelines for the use and interpretation of assays for monitoring autophagy.

16. Guidelines for the use and interpretation of assays for monitoring autophagy.

17. Guidelines for the use and interpretation of assays for monitoring autophagy.

20. Interplay between SUMOylation and NEDDylation regulates RPL11 localization and function

21. BioTIME: A database of biodiversity time series for the Anthropocene

22. Elevated Level of DNA Damage and Impaired Repair of Oxidative DNA Damage in Patients with Recurrent Depressive Disorder

23. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

24. Erratum

25. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

26. PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia

27. The phage tail tape measure protein, an inner membrane protein and a periplasmic chaperone play connected roles in the genome injection process of E. coli phage HK97

28. Analysis of the genome and transcriptome of [i]Cryptococcus neoformans[/i] var.[i] grubii[/i] reveals complex RNA expression and microevolution leading to virulence attenuation

30. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

31. The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

32. Individual common variants exert weak effects on the risk for autism spectrum disorderspi

33. Epidemiology and Evolution of Fungal Pathogens in Plants and Animals

34. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

35. A 2022 τ-Herculids meteor cluster

36. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

37. Sertoli cell Dicer is essential for spermatogenesis in mice

38. Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates

39. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

43. Ion channel profiling of the Lymnaea stagnalis ganglia via transcriptome analysis

46. Global Proximity Interactome of the Human Macroautophagy Pathway

47. SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

48. Glial contribution to cyclodextrin-mediated reversal of cholesterol accumulation in murine NPC1-deficient neurons in vivo

49. Salmonella effector sopd promotes plasma membrane scission by inhibiting rab10

50. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder

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