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1. Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature.

3. Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice

4. Structural aging of human neurons is the opposite of the changes in schizophrenia

5. Oxytocin-induced increases in cytokines and clinical effect on the core social features of autism: Analyses of RCT datasets

6. De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues

8. Structural diverseness of neurons between brain areas and between cases

9. Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

10. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

11. Three-dimensional alteration of neurites in schizophrenia

12. Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes

13. Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

14. Copy number variations in RNF216 and postsynaptic membrane–associated genes are associated with bipolar disorder: a case‐control study in the Japanese population.

16. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

19. Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature

24. Effect of intranasal oxytocin on the core social symptoms of autism spectrum disorder: a randomized clinical trial

25. Structural diverseness of neurons between brain areas and between cases

27. Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study.

29. Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility

30. ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

31. Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus

32. Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

33. Structural aging of human neurons is opposite of the changes in schizophrenia

35. The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder

40. Molecular diagnosis of 405 individuals with autism spectrum disorder

41. De novo MCM6 variants in neurodevelopmental disorders:a recognizable phenotype related to zinc binding residues

42. Molecular diagnosis of 405 individuals with autism spectrum disorder

43. Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

44. Three-dimensional alteration of neurites in schizophrenia

45. Analysis of human neuronal cells carrying ASTN2 deletion: A cross-disorder risk variant of schizophrenia, autism spectrum disorder, and bipolar disorder

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