Gregor Johann Mendel and the beginning of genetics

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained.

Leukemia·2006

FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature.

Leukemia research·2006

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia.

British journal of haematology·2005

Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1.

Leukemia·2003

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma.

Bone marrow transplantation·2003

Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma.

Leukemia·2003

Impact of a Nationwide Remote Patient Care Hypertension Program on Clinical and Health Care Cost and Utilization Outcomes.

Mayo Clinic proceedings·2026

"You'll be Fine. Probably." Communicating Risk in Clinical Medicine.

Mayo Clinic proceedings·2026

The Optimal Timing for Patients With Acute Myocardial Infarction to Safely Undergo Elective Non-Cardiac Surgery: A Retrospective Cohort Study.

Mayo Clinic proceedings·2026

Topical Therapy for the Internist: A Practical Framework for Safer Prescribing.

Mayo Clinic proceedings·2026

Treatment of Parkinson Disease.

Mayo Clinic proceedings·2026

Navigating Protein-Losing Enteropathy: A Stepwise Approach for Primary Care Clinicians.

Mayo Clinic proceedings·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Genes·2026

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Journal of immigrant and minority health·2026

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Stem cell research·2026

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

Diseases (Basel, Switzerland)·2026

Related Experiment Videos

Gregor Johann Mendel and the beginning of genetics

Related Concept Videos

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained.

FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature.

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia.

Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1.

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma.

Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma.

Impact of a Nationwide Remote Patient Care Hypertension Program on Clinical and Health Care Cost and Utilization Outcomes.

"You'll be Fine. Probably." Communicating Risk in Clinical Medicine.

The Optimal Timing for Patients With Acute Myocardial Infarction to Safely Undergo Elective Non-Cardiac Surgery: A Retrospective Cohort Study.

Topical Therapy for the Internist: A Practical Framework for Safer Prescribing.

Treatment of Parkinson Disease.

Navigating Protein-Losing Enteropathy: A Stepwise Approach for Primary Care Clinicians.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

Related Experiment Videos

Gregor Johann Mendel and the beginning of genetics

Related Concept Videos

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