Regional localization of the human thrombomodulin gene to 20p12-cen

Familial Lymphoproliferative Disorders with Chromosomal Fragile Site Analysis.

Leukemia & lymphoma·2016

Myeloid Leukemia After Cytotoxic Therapy and Other Hematotoxins.

Hematology (Amsterdam, Netherlands)·2016

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.

Journal of thrombosis and haemostasis : JTH·2016

Appendix II: A revised classification of Von Willebrand disease*: For The Subcommittee on Von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

Linker regions and flexibility around the metalloprotease domain account for conformational activation of ADAMTS-13.

Journal of thrombosis and haemostasis : JTH·2015

Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM).

Leukemia·2015

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Genomics·2026

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

Genomics·2026

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Genomics·2026

Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

Genomics·2026

Genomic signatures of the Arctic-adapted North American gray wolf ecotype.

Genomics·2026

HIF-1 signaling contributes to lenvatinib resistance in patient-derived HCC organoids.

Genomics·2026

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Neurogenetics·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

European journal of pediatrics·2026

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Naunyn-Schmiedeberg's archives of pharmacology·2026

Related Experiment Videos

Regional localization of the human thrombomodulin gene to 20p12-cen

Related Concept Videos

Familial Lymphoproliferative Disorders with Chromosomal Fragile Site Analysis.

Myeloid Leukemia After Cytotoxic Therapy and Other Hematotoxins.

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.

Appendix II: A revised classification of Von Willebrand disease*: For The Subcommittee on Von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Linker regions and flexibility around the metalloprotease domain account for conformational activation of ADAMTS-13.

Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM).

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

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Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

Genomic signatures of the Arctic-adapted North American gray wolf ecotype.

HIF-1 signaling contributes to lenvatinib resistance in patient-derived HCC organoids.

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

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Regional localization of the human thrombomodulin gene to 20p12-cen

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