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6. Deep Learning for Automatic Detection and Facial Recognition in Japanese Macaques: Illuminating Social Networks

7. A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins.

15. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

19. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

20. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

23. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

24. Improving access to exome sequencing in a medically underserved population through the Texome Project

29. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

30. De novo variants in DENND5B cause a neurodevelopmental disorder

31. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

32. Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling

34. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

35. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

42. Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies

45. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

46. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

47. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

48. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

50. Differences among epitopes recognized by neutralizing antibodies induced by SARS-CoV-2 infection or COVID-19 vaccination

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