Pages that link to "Q42689580"
Jump to navigation
Jump to search
The following pages link to Vincent Schulz (Q42689580):
Displaying 50 items.
- The pattern of polymorphism in Arabidopsis thaliana (Q21146096) (← links)
- A multiprotein complex necessary for both transcription and DNA replication at the β-globin locus (Q24298193) (← links)
- Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment (Q24317106) (← links)
- Human and murine erythropoiesis (Q27023709) (← links)
- Saccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA. (Q27938991) (← links)
- Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation (Q28117414) (← links)
- Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results (Q28250059) (← links)
- Tcf7 is an important regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell line (Q28481434) (← links)
- Molecular phenotypes in triple negative breast cancer from African American patients suggest targets for therapy (Q28535227) (← links)
- Serum response factor is an essential transcription factor in megakaryocytic maturation (Q28586357) (← links)
- Identification of biologically relevant enhancers in human erythroid cells (Q30441416) (← links)
- Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo (Q30500396) (← links)
- Role for MKL1 in megakaryocytic maturation (Q33382736) (← links)
- MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation (Q33402409) (← links)
- EBNA1 regulates cellular gene expression by binding cellular promoters (Q33563969) (← links)
- MixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cells (Q33598607) (← links)
- Global transcriptome analyses of human and murine terminal erythroid differentiation (Q33697238) (← links)
- X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils (Q33734823) (← links)
- Schizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicases (Q33899410) (← links)
- Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells (Q34052591) (← links)
- Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis (Q34270548) (← links)
- Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl. (Q34383771) (← links)
- Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes. (Q34444243) (← links)
- Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration. (Q34803107) (← links)
- GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arrays (Q35087993) (← links)
- Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expression (Q35604396) (← links)
- CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells (Q36027873) (← links)
- Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis (Q36051078) (← links)
- The blood transcriptional signature of chronic hepatitis C virus is consistent with an ongoing interferon-mediated antiviral response (Q36515443) (← links)
- DNA polymerase β variant Ile260Met generates global gene expression changes related to cellular transformation (Q36727506) (← links)
- A procedure for highly specific, sensitive, and unbiased whole-genome amplification (Q36926786) (← links)
- Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes (Q37374740) (← links)
- Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia (Q37695066) (← links)
- Favorable outcome associated with an IGF-1 ligand signature in breast cancer (Q38328093) (← links)
- Estrogen Drives Cellular Transformation and Mutagenesis in Cells Expressing the Breast Cancer-Associated R438W DNA Polymerase Lambda Protein. (Q38733937) (← links)
- NFBD1/MDC1 regulates Cav1 and Cav2 independently of DNA damage and p53. (Q39546495) (← links)
- Valproic acid antagonizes the capacity of other histone deacetylase inhibitors to activate the Epstein-barr virus lytic cycle. (Q39575256) (← links)
- Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability (Q41898543) (← links)
- Nonstochastic reprogramming from a privileged somatic cell state (Q42029224) (← links)
- Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus (Q43135443) (← links)
- Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis (Q45051449) (← links)
- STAT4 and T-bet control follicular helper T cell development in viral infections. (Q47355847) (← links)
- Molecular basis of tactile specialization in the duck bill. (Q47809659) (← links)
- Distinct roles for TET family proteins in regulating human erythropoiesis (Q50216979) (← links)
- Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis. (Q50885324) (← links)
- Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype. (Q51340480) (← links)
- A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes. (Q53476832) (← links)
- Late-onset Leclercia adecarboxylata sepsis in a premature neonate (Q57250839) (← links)
- Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing (Q57250847) (← links)
- In vitro secondary structure analysis of mRNA from lacZ translation initiation mutants (Q57250866) (← links)