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2. Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

4. Myelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylation

7. The Addiction-Susceptibility TaqIA/Ankk1 Controls Reward and Metabolism Through D2 Receptor-Expressing Neurons

11. CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

15. CREBBP lysine acetyltransferase domain mutations create zombie enzymes that alter chromatin loading dynamics and prevent EP300 redundancy

16. UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking

18. Crebbp loss cooperates with Bcl2 overexpression to promote lymphoma in mice

20. Intracellular Signal Modulation by Nanomaterials

26. Interplay between EGFR, E-cadherin, and PTP1B in epidermal homeostasis.

28. The addiction-susceptibility TaqIA/Ankyrin repeat and kinase domain containing 1 kinase (ANKK1) controls reward and metabolism through dopamine receptor type 2 (DR2)-expressing neurons

29. HDAC1 and PRC2 mediate combinatorial control in SPI1/PU.1-dependent gene repression in murine erythroleukaemia

32. Biochemical, Enzymatic, and Computational Characterization of Recurrent Somatic Mutations of the Human Protein Tyrosine Phosphatase PTP1B in Primary Mediastinal B Cell Lymphoma

34. A readout of metabolic efficiency in arylamine N ‐acetyltransferase‐deficient mice reveals minor energy metabolism changes

36. Systemic inflammatory syndrome in children with FARSA deficiency

39. The Benzene Hematotoxic and Reactive Metabolite 1,4-Benzoquinone Impairs the Activity of the Histone Methyltransferase (SETD2) and Causes Aberrant Histone H3K36 Trimethylation (H3K36me3)

44. The Benzene Hematotoxic and Reactive Metabolite 1,4-Benzoquinone Impairs the Activity of the Histone Methyltransferase SET Domain Containing 2 (SETD2) and Causes Aberrant Histone H3 Lysine 36 Trimethylation (H3K36me3)

48. Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus

49. Loss-of-Function Mutation in PTPN2 Causes Aberrant Activation of JAK Signaling Via STAT and Very Early Onset Intestinal Inflammation

50. Cloning and molecular characterization of three arylamine N-acetyltransferase genes from bacillus anthracis: Identification of unusual enzymatic properties and their contribution to sulfamethoxazole resistance

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