259 results on '"Moresco, Eva Marie Y."'
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2. Dynamic molecular architecture and substrate recruitment of cullin3–RING E3 ligase CRL3KBTBD2
3. OVOL2 sustains postnatal thymic epithelial cell identity
4. Trans-Golgi protein TVP23B regulates host-microbe interactions via Paneth cell homeostasis and Goblet cell glycosylation
5. De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes
6. Sulfatides are endogenous ligands for the TLR4–MD-2 complex
7. Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning
8. Viable mutations of mouse midnolin suppress B cell malignancies
9. Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesis
10. Loss of immunity-related GTPase GM4951 leads to nonalcoholic fatty liver disease without obesity
11. Disruption of the ZFP574-THAP12 complex suppresses B cell malignancies in mice.
12. Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice
13. Genetic and structural studies of RABL3 reveal an essential role in lymphoid development and function
14. Essential role of MFSD1-GLMP-GIMAP5 in lymphocyte survival and liver homeostasis
15. Essential requirement for IER3IP1 in B cell development
16. Enhanced susceptibility to chemically induced colitis caused by excessive endosomal TLR signaling in LRBA-deficient mice
17. Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex function
18. N4BP1 negatively regulates NF-κB by binding and inhibiting NEMO oligomerization
19. Syndromic immune disorder caused by a viable hypomorphic allele of spliceosome component Snrnp40
20. The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
21. Adjuvant effect of the novel TLR1/TLR2 agonist Diprovocim synergizes with anti–PD-L1 to eliminate melanoma in mice
22. ENU-induced phenovariance in mice: inferences from 587 mutations
23. Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
24. IgD class switching is initiated by microbiota and limited to mucosa-associated lymphoid tissue in mice
25. Insulin resistance and diabetes caused by genetic or diet-induced KBTBD2 deficiency in mice
26. Essential role of MFSD1-GLMP-GIMAP5 in lymphocyte survival and liver homeostasis.
27. Essential requirement for IER3IP1 in B cell development.
28. TLR4/MD-2 activation by a synthetic agonist with no similarity to LPS
29. Real-time resolution of point mutations that cause phenovariance in mice
30. MAVS, cGAS, and endogenous retroviruses in T-independent B cell responses
31. Mutation of mouse Samd4 causes leanness, myopathy, uncoupled mitochondrial respiration, and dysregulated mTORC1 signaling
32. Abl Family Kinases in Mammalian Development
33. Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing
34. Next-Generation Diprovocims with Potent Human and Murine TLR1/TLR2 Agonist Activity That Activate the Innate and Adaptive Immune Response
35. Modulation of autoimmune diabetes by N-ethyl-N-nitrosourea- induced mutations in non-obese diabetic mice
36. RNPS1 inhibits excessive tumor necrosis factor/tumor necrosis factor receptor signaling to support hematopoiesis in mice
37. Yip1 domain family, member 6 (Yipf6) mutation induces spontaneous intestinal inflammation in mice
38. Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet
39. Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype
40. Flt3 permits survival during infection by rendering dendritic cells competent to activate NK cells
41. LGP2: Positive about Viral Sensing
42. Inflammation and Autoimmunity Caused by a SHP1 Mutation Depend on IL-1, MyD88, and a Microbial Trigger
43. A Catechol-O-Methyltransferase That Is Essential for Auditory Function in Mice and Humans
44. The Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency
45. HUMORAL IMMUNITY: MAVS, cGAS, and endogenous retroviruses in T-independent B cell responses
46. SLFN2 protection of tRNAs from stress-induced cleavage is essential for T cell–mediated immunity
47. An Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence
48. Bulk segregation mapping of mutations in closely related strains of mice
49. RNPS1 inhibits excessive tumor necrosis factor/tumor necrosis factor receptor signaling to support hematopoiesis in mice.
50. De novo germline mutation in the Dual Specificity Phosphatase 10 gene accelerates autoimmune diabetes in Non-Obese Diabetic (NOD) mice
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