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509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II
509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II
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509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II
509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II
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Conferences and Meetings
Short name:
updated-509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II-2023
Course start date:
01/12/2026
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509. Bone Marrow Failure and Cancer Predisposition Syndromes: Congenital: Poster II
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Loss of EFL1 Which Causes a Shwachman-Diamond Syndrome Reduces Cell Proliferation and Alters Transcriptional Profiling during Neutrophil Differentiati
1 activities
Loss of EFL1 Which Causes a Shwachman-Diamond Syndrome Reduces Cell Proliferation and Alters Transcriptional Profiling during Neutrophil Differentiati
Polygenic Modifiers of Expressivity in Telomere Biology Disorders
1 activities
Polygenic Modifiers of Expressivity in Telomere Biology Disorders
Targeting Nucleotide Biosynthesis Ameliorates Neutropenia in a Zebrafish Model of Dnajc21-Mutant Shwachman-Diamond Syndrome
1 activities
Targeting Nucleotide Biosynthesis Ameliorates Neutropenia in a Zebrafish Model of Dnajc21-Mutant Shwachman-Diamond Syndrome
Impact of Dkc1 Deficiency on BM Niche Function during Hematopoietic Stem Cell Transplantation in a Conditional Murine Model of X-Linked Dyskeratosis C
1 activities
Impact of Dkc1 Deficiency on BM Niche Function during Hematopoietic Stem Cell Transplantation in a Conditional Murine Model of X-Linked Dyskeratosis C
Metabolomic Profiling Confirms the Key Role of Oxidative Stress in the Pathophysiology of Diamond-Blackfan Anemia
1 activities
Metabolomic Profiling Confirms the Key Role of Oxidative Stress in the Pathophysiology of Diamond-Blackfan Anemia
RUNX1 Germline Mutations of Autosomal-Dominant Familial Platelet Disorder Are More Common Than Expected in Adult Myeloid Leukemias Indicating Highly V
1 activities
RUNX1 Germline Mutations of Autosomal-Dominant Familial Platelet Disorder Are More Common Than Expected in Adult Myeloid Leukemias Indicating Highly V
A Zebrafish Model of Parn-Deficiency Reveals Conserved Mechanisms Underlying Marrow Failure and Opportunities for Therapeutic Amelioration of Hematopo
1 activities
A Zebrafish Model of Parn-Deficiency Reveals Conserved Mechanisms Underlying Marrow Failure and Opportunities for Therapeutic Amelioration of Hematopo
Genetic Profile of Myeloid Neoplasms Developed with Fanconi Anemia and Aldehyde Degradation Deficiency Syndrome
1 activities
Genetic Profile of Myeloid Neoplasms Developed with Fanconi Anemia and Aldehyde Degradation Deficiency Syndrome
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