14478 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

in 16.69 milliseconds.

• CD3 bispecific antibody-induced cytokine release is dispensable for cytotoxic T cell activity

  Study EGAS00001003734

• DAC Committee for the "PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma" study

  Dac EGAC00001002371

• Microbiome confounders and quantitative profiling challenge established microbial targets in colorectal cancer developmental stages

  Study EGAS00001007413

• Genomic validation of the revised Bethesda criteria in terms of pathogenesis and oncologic significance

  Study EGAS00001003959

• RNA sequencing of lung fibroblasts

  RNA sequencing of lung fibroblasts

  Study EGAS00001007857

• CAGEKID: Cancer Genomics of the Kidney

  Study EGAS00001000083

• Accurate mutation detection in leukemia by re-sequencing a cancer gene set

  Study EGAS00001000268

• Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia

  Study EGAS00001000296

• Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing

  Study EGAS00001000850

• Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH

  Study EGAS00001002618

• Activation of IL7RA signalling in human B-lymphoid precursors induces pre-leukemia

  Study EGAS00001003979

• Extreme intratumor heterogeneity and driver evolution in mismatch repair deficient gastro-esophageal cancer

  Study EGAS00001003434

• PBMC gene expression profiles in diet treated celiac disease upon oral gluten challenge

  Study EGAS00001004860

• Biological and Therapeutic Implications of a Unique Subtype of NPM1 Mutated AML

  Study EGAS00001004872

• Inherited CD28 deficiency in otherwise healthy patients with disseminated warts and giant horns

  Study EGAS00001004837

• Single cell RNA sequencing of 33 primary colorectal cancer

  Study EGAS00001003779

• CRISPR-based adenine editors correct nonsense mutations in a cystic fibrosis organoid biobank.

  Study EGAS00001003951

• The whole genome landscape of Burkitt lymphoma subtypes

  Study EGAS00001003778

• Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia'

  Study EGAS00001005171

• Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma

  Study EGAS00001004288

• Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia

  Study EGAS00001005820

• Longitudinal Single Cell Atlas of COVID-19 Identifies an Early, Transient Prognostic Signature

  Study EGAS00001005545

• Minor intron splicing efficiency increases with the development of lethal prostate cancer

  Study EGAS00001005546

• Absolute copy number fitting from shallow whole genome sequencing data

  Study EGAS00001005601

• WGS of iPSC from TOF patients with/without DG and healthy control

  Study EGAS00001006035

• A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome

  Study EGAS00001006280

• CDK4 phosphorylation predicts high sensitivity of malignant pleural mesotheliomas to CDK4/6 inhibition

  Study EGAS00001006117

• miRNA regulation of monocyte expressed inflammatory genes in patients with inflammatory bowel disease

  Study EGAS00001006157

• Serum Proteome Profiling Identifies Early Markers of Therapeutic Response to Neoadjuvant Chemotherapy of Breast Cancer

  Study EGAS00001006228

• Genomics characterization of BRAF-V600E colorectal cancer patients treated with anti-BRAF/EGFR

  Study EGAS00001006247

• Genetic Determinants of Mannose-binding Lectin Activity Predispose to Thromboembolic Complications in Critical COVID-19

  Study EGAS00001006266

• Comprehensive Whole-Genome Sequence Annotation to Resolve the Genetic Architecture of Cerebral Palsy

  Study EGAS00001006724

• Tertiary lymphoid structure signatures are associated with immune checkpoint inhibitor related acute interstitial nephritis

  Study EGAS00001006781

• The genome-wide mutational consequences of DNA hypomethylation

  Study EGAS00001006845

• Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells

  Study EGAS00001007026

• Gene expression of neutrophils in response to Mtb infection in persons living with HIV

  Study EGAS00001007262

• Healthy human B-lymphopoiesis RNA-Seq reference using FACS sorted bone marrow aspirates

  Study EGAS00001007305

• Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans

  Study EGAS00001007423

• Single-cell dissection of the immune response after a myocardial infarction

  Study EGAS00001007021

• Induction Failure in Childhood and Young Adult T-cell Acute Lymphoblastic Leukemia

  Study EGAS00001006411

• Accessibility Over Transposable Elements Reveals Genetic Determinants of Stemness Properties in Normal and Leukemic Hematopoiesis

  Study EGAS00001007191

• Disturbed trophoblast transition links early fetal to maternal syndrome progression in pre-eclampsia

  Study EGAS00001005681

• APL nanopore sequencing

  Nanopore sequencing for an APL patient

  Study EGAS00001005618

• Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS

  Study EGAS00001006800

• HCA_Heart_Adult_Wellcome_DNA

  Human Cell Atlas - WGS Adult Heart

  Study EGAS00001006359

• Epigenomic profile of diverse cancer

  Epigenomic profile of diverse cancer.

  Study EGAS00001004352

• Paediatric Tumour Profiling

  Paediatric Tumour Profiling

  Study EGAS00001003437

• Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq

  Study EGAS00001006802

• Genome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome

  Study EGAS00001006371

• Genetic landscape of pediatric Retinoblastoma

  Study EGAS00001000346