Monoclonal Gammopathy Of Undetermined Significance
What's New
Last Posted: Aug 30, 2024
- FCGR3A F158V alleles frequency differs in multiple myeloma patients from healthy population.
Michaël Constantinides, et al. Oncoimmunology 2024 0 (1) 2388306 - Clinical Implications of Genomic Profile in Waldenström Macroglobulinemia.
David F Moreno, et al. Hematology/oncology clinics of North America 2023 0 - Mutational Profile in 75 Patients With Anti-Myelin-Associated Glycoprotein Neuropathy: Clinical and Hematologic Therapy Response and Hints on New Therapeutic Targets.
Francesca Castellani, et al. Neurology(R) neuroimmunology & neuroinflammation 2023 0 (4) - Detection of complex genomic signatures associated with risk in plasma cell disorders.
Berry Nadine K, et al. Cancer genetics 2017 0 1-9 - Detection of MYD88 L265P mutation by next-generation deep sequencing in peripheral blood mononuclear cells of Waldenström's macroglobulinemia and IgM monoclonal gammopathy of undetermined significance.
Nakamura Ayako, et al. PloS one 2019 0 (9) e0221941 - A risk-stratification model based on the initial concentration of the serum monoclonal protein and MYD88 mutation status identifies a subset of patients with IgM monoclonal gammopathy of undetermined significance at high risk of progression to Waldenström macroglobulinaemia or other lymphoproliferative disorders.
Varettoni Marzia, et al. British journal of haematology 2019 0 (4) 441-446 - Genomic Profiling of Smoldering Multiple Myeloma Identifies Patients at a High Risk of Disease Progression.
Bustoros Mark, et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2020 0 (21) 2380-2389 - Telomere Architecture Correlates with Aggressiveness in Multiple Myeloma.
Rangel-Pozzo Aline, et al. Cancers 2021 0 (8) - Artificial intelligence-enabled screening strategy for drug repurposing in monoclonal gammopathy of undetermined significance.
Alexander J Ryu et al. Blood cancer journal 2023 13(1) 28 - Flow cytometry detection of CD138 expression continuum between monotypic B and plasma cells is associated with both high IgM peak levels and MYD88 mutation and contributes to diagnosis of Waldenström macroglobulinemia.
Gayet Mylene, et al. Cytometry. Part B, Clinical cytometry 2021 0 (1) 62-69
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: