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

4. OXR1 maintains the retromer to delay brain aging under dietary restriction

7. Promoting validation and cross-phylogenetic integration in model organism research

8. Regulation of Drosophila oviduct muscle contractility by octopamine

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

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

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

14. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

15. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

16. Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma

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

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

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

21. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

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

25. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development

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

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

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

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

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

31. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

32. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

34. Drosophila Voltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains

35. Novel role of dynamin‐related‐protein 1 in dynamics of ER‐lipid droplets in adipose tissue

36. Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly

38. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

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

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

42. Alzheimer’s disease risk allele of PICALM causes detrimental lipid droplets in microglia

44. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

45. De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects

46. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis

47. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.

48. IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells

49. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

50. Interactions between the Ig-Superfamily Proteins DIP-α and Dpr6/10 Regulate Assembly of Neural Circuits

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