Fibrosarcoma
What's New
Last Posted: Jun 08, 2023
- Efficient Identification of Patients With NTRK Fusions Using a Supervised Tumor-Agnostic Approach.
Susana Hernandez et al. Arch Pathol Lab Med 2023 - Novel cataract-causing variant c.177dupC in c-MAF regulates the expression of crystallin genes for cell apoptosis via a mitochondria-dependent pathway.
Li Li, et al. Molecular genetics and genomics : MGG 2023 0 (2) 495-506 - Survival Outcomes in Patients With RAS Wild Type Metastatic Colorectal Cancer Classified According to Köhne Prognostic Category and BRAF Mutation Status.
Siena Salvatore, et al. Clinical colorectal cancer 2017 0 (1) 50-57.e8 - Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis.
Imani Mohammad Moslem, et al. International journal of environmental research and public health 2019 0 (15) - Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation.
Ferreira Amanda Meneses, et al. The Journal of steroid biochemistry and molecular biology 2019 0 250-255 - Broadening the genotypic and phenotypic spectrum of MAF in three Chinese Han congenital cataracts families.
Wang Qiwei, et al. American journal of medical genetics. Part A 2022 0 (10) 2888-2898 - Association of Single-Nucleotide Polymorphisms of MAFB Gene with Nonsyndromic Cleft Lip with or without Cleft Palate in Kinh Vietnamese Patients.
Phan Hoanh Duy Ba, et al. Indian journal of plastic surgery : official publication of the Association of Plastic Surgeons of India 2022 0 (1) 70-74 - BRAF V600E and previously unidentified KRAS G12C mutations in odontogenic tumors may affect MAPK activation differently depending on tumor type.
Oh Kyu-Young, et al. Genes, chromosomes & cancer 2022 0 (8) 481-490 - Breast cancer cases of female patients under 35 years of age in Togo: A series of 158 cases.
Darré Tchin, et al. Molecular and clinical oncology 2017 0 (6) 1125-1129 - Impact of phosphoinositide-3-kinase and vitamin D3 nuclear receptor single-nucleotide polymorphisms on the outcome of malignant melanoma patients.
Morgese Francesca, et al. Oncotarget 2017 11 (44) 75914-75923 - NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome.
Zhao Xiaonan et al. JCO precision oncology 2021 1 - Canadian Consensus for Biomarker Testing and Treatment of TRK Fusion Cancer in Pediatric Patients.
Perreault Sébastien et al. Current oncology (Toronto, Ont.) 2021 Jan 28(1) 346-366 - Association between MAFB rs17820943 and rs6072081 polymorphism and risk of nonsyndromic cleft lip with or without cleft palate: a meta-analysis.
Liang X, et al. The British journal of oral & maxillofacial surgery 2020 7 - Gene-gene interactions between BMP4 and ARHGAP29 among non-syndromic cleft lip only (NSCLO) trios from western Han Chinese population.
Wang Yiru, et al. International journal of clinical and experimental pathology 2020 0 (2) 295-301 - ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.
Scotto di Carlo Federica, et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2020 2 - TRK Fusion Cancers in Children: A Clinical Review and Recommendations for Screening.
Albert Catherine M et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2019 37(6) 513-524 - Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li-Fraumeni syndrome).
Petry Vanessa, et al. Familial cancer 2019 11 - 'Revolutionary' new class of cancer drugs approved
J Gallagher, BBC News, September 23, 2019 - Population-level effect of molecular testing and targeted therapy in patients with advanced pulmonary adenocarcinoma: a prospective cohort study.
Schwegler Christine, et al. Virchows Archiv : an international journal of pathology 2018 4 (4) 581-588 - A common variant of MAF/c-MAF, transcriptional factor gene in the kidney, is associated with gout susceptibility.
Higashino Toshihide, et al. Human cell 2018 1 (1) 10-13 - Clinical, histopathological, and molecular analyses of IDH-wild-type WHO grade II-III gliomas to establish genetic predictors of poor prognosis.
Kuwahara Kiyonori, et al. Brain tumor pathology 2019 7 - A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes.
Si Nuo, et al. Gene 2019 1 113-118 - Fibroblastic and myofibroblastic tumors of children: new genetic entities and new ancillary testing.
Parham David M et al. F1000Research 2018 7 - FDA approves Āprecision medicineĀ drug for different cancers with same mutation
L McGinley, Washington Post, November 26, 2018 - A rare variant at 11p13 is associated with tuberculosis susceptibility in the Han Chinese population.
Chen Cheng, et al. Scientific reports 2016 0 24016 - Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study.
Yang Qian, et al. Lipids in health and disease 2015 0 (1) 79 - Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China.
Mi Na, et al. The British journal of oral & maxillofacial surgery 2014 10 (8) 746-50 - Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias.
Sarhadi Virinder Kaur, et al. Genes, chromosomes & cancer 2014 7 (7) 579-88 - Further evidence of association of the ABCA4 gene with cleft lip/palate.
Fontoura C, et al. European journal of oral sciences 2012 12 (6) 6 - [Association between single nucleotide polymorphisms of v-maf musculoaponeurotic fibrosarcoma oncogene homolog B gene and non-syndromic cleft lip with or without cleft palate].
Cheng Hongqiu, et al. Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery 2012 7 (7) 845-8
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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
- Page last updated:May 03, 2024
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