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1. APDS patients with immune-complex vasculitis and resolution with leniolisib

2. A Clinicopathological Categorization System for Clinical Research in Coccidioidomycosis

3. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

4. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

5. Tuning immunity through tissue mechanotransduction

6. Systemic enhancement of antitumour immunity by peritumourally implanted immunomodulatory macroporous scaffolds

7. Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome (NODRS)

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

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

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

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

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

14. Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defect with accumulation of T-bet+ B cells

15. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

16. IL‐10 promotes endothelial progenitor cell infiltration and wound healing via STAT3

17. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

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

21. De novo variants in DENND5B cause a neurodevelopmental disorder

23. Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples

24. Immunomodulatory microneedle patch for periodontal tissue regeneration

25. Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

26. Biallelic PI4KA variants cause neurological, intestinal and immunological disease

27. Expanding the potential genes of inborn errors of immunity through protein interactions

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

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

31. Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors

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

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

34. When Screening for Severe Combined Immunodeficiency (SCID) with T Cell Receptor Excision Circles Is Not SCID: a Case-Based Review

35. Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers.

36. CADINS in an Adult with Chronic Sinusitis and Atopic Disease

37. Multiplexed Functional Assessment of Genetic Variants in CARD11

38. Unraveling the mechanobiology of immune cells.

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

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

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

42. Augmenting T-cell responses to tumors by in situ nanomanufacturing

43. Progressive B Cell Loss in Revertant X-SCID

44. T-cell activation is modulated by the 3D mechanical microenvironment

45. Mechanosensing through YAP controls T cell activation and metabolism

46. Disseminated Coccidioidomycosis Treated with Interferon-γ and Dupilumab

47. Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.

48. The Role of the Anti-Inflammatory Cytokine Interleukin-10 in Tissue Fibrosis

49. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

50. Differential Contributions of Actin and Myosin to the Physical Phenotypes and Invasion of Pancreatic Cancer Cells.

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