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251. Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen

252. Interferon autoantibodies associated with AIRE-deficiency decrease the expression of IFN-stimulated genes

254. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia

257. Thymic Deletion and Regulatory T Cells Prevent Antimyeloperoxidase GN

258. Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing.

260. Autoimmune Polyendocrine Syndrome Type 1 : NALP5 in Autoimmune Polyendocrine Syndrome Type 1

261. Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis

263. Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia

264. Proteomic and Metabolomic Analyses of Mitochondrial Complex I-deficient Mouse Model Generated by Spontaneous B2 Short Interspersed Nuclear Element (SINE) Insertion into NADH Dehydrogenase (Ubiquinone) Fe-S Protein 4 (Ndufs4) Gene

266. Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature

268. ASXL1and BIMgerm line variants predict response and identify CML patients with the greatest risk of imatinib failure

269. A network-biology perspective of microRNA function and dysfunction in cancer

271. DNA methylation signatures of the AIRE promoter in thymic epithelial cells, thymomas and normal tissues

272. Mechanisms of Co-Operation of DNMT3A Mutations with JAK2 V617F Through Histone H4 Arginine 3 Provides New Insights in MPN Disease Pathogenesis

275. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

276. Aire regulates the transfer of antigen from mTECs to dendritic cells for induction of thymic tolerance

278. Autoimmune regulator (AIRE)-deficient CD8+CD28lowregulatory T lymphocytes fail to control experimental colitis

279. Tmprss3, a Transmembrane Serine Protease Deficient in Human DFNB8/10 Deafness, Is Critical for Cochlear Hair Cell Survival at the Onset of Hearing

280. Deep sequencing analysis of the developing mouse brain reveals a novel microRNA

281. DNMT3L Is a Regulator of X Chromosome Compaction and Post-Meiotic Gene Transcription

282. RUNX1 mutations are rare in chronic phase polycythaemia vera

283. Investigating the Potential Role of Genetic and Epigenetic Variation of DNA Methyltransferase Genes in Hyperplastic Polyposis Syndrome

284. Increased IL-17A secretion in response to Candida albicans in autoimmune polyendocrine syndrome type 1 and its animal model

285. GATA2 is a New Predisposition Gene for Familial Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML)

286. Detection of Low Level Nilotinib or Dasatinib Resistant BCR-ABL Mutations by Mass Spectrometry In CML Patients Who Fail Imatinib Is Highly Predictive of Their Subsequent Clonal Expansion When Treated with the Drug for Which Their Mutation Confers Resistance

290. Spatiotemporal Regulation of Multiple Overlapping Sense and Novel Natural Antisense Transcripts at the Nrgn and Camk2n1 Gene Loci during Mouse Cerebral Corticogenesis

293. Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes

294. Diversity and clonotypic composition of influenza-specific CD8+TCR repertoires remain unaltered in the absence of Aire

295. Short-term inhibition of p53 combined with keratinocyte growth factor improves thymic epithelial cell recovery and enhances T-cell reconstitution after murine bone marrow transplantation

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