Inflammatory Breast Cancer
What's New
Last Posted: Nov 04, 2024
- Whole-exome profiles of inflammatory breast cancer and pathological response to neoadjuvant chemotherapy.
François Bertucci, et al. Journal of translational medicine 2024 0 (1) 969 - DNA methylation profile of inflammatory breast cancer and its impact on prognosis and outcome.
Flavia Lima Costa Faldoni, et al. Clinical epigenetics 2024 0 (1) 89 - Clinicogenomic characterization of inflammatory breast cancer.
Nolan Priedigkeit, et al. bioRxiv : the preprint server for biology 2024 0 - Mutational landscape of inflammatory breast cancer.
François Bertucci, et al. Journal of translational medicine 2024 0 (1) 374 - Rates of immune cell infiltration in patients with triple-negative breast cancer by molecular subtype.
Harano Kenichi, et al. PloS one 2018 0 (10) e0204513 - Inflammatory Breast Cancer: Clinical Implications of Genomic Alterations and Mutational Profiling.
Faldoni Flávia L C, et al. Cancers 2020 0 (10) - Whole-exome sequencing identifies somatic mutations and intratumor heterogeneity in inflammatory breast cancer.
Luo Rui, et al. NPJ breast cancer 2021 0 (1) 72 - Characteristics associated with inflammatory breast cancer (IBC): An epidemiologic study from a dedicated IBC program.
White Randie E et al. The breast journal 2020 Sep - Genetic Variants Detected Using Cell-Free DNA from Blood and Tumor Samples in Patients with Inflammatory Breast Cancer.
Winn Jennifer S, et al. International journal of molecular sciences 2020 2 (4) - BRCA mutations in women with inflammatory breast cancer.
Gutierrez Barrera Angelica M, et al. Cancer 2018 0 (3) 466-474
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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
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