Terms: = Sarcomas AND MEN1, ENSG00000133895, 4221
20 results:
1. Cancer predisposition genes in Japanese children with rhabdomyosarcoma.
Fukushima H; Suzuki R; Yamaki Y; Hosaka S; Inaba M; Morii W; Noguchi E; Takada H
J Hum Genet; 2022 Jan; 67(1):35-41. PubMed ID: 34257391
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2. Whole-genome Sequencing of Follicular Thyroid Carcinomas Reveal Recurrent Mutations in MicroRNA Processing Subunit DGCR8.
Paulsson JO; Rafati N; DiLorenzo S; Chen Y; Haglund F; Zedenius J; Juhlin CC
J Clin Endocrinol Metab; 2021 Oct; 106(11):3265-3282. PubMed ID: 34171097
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3. Integrated mutational landscape analysis of uterine leiomyosarcomas.
Choi J; Manzano A; Dong W; Bellone S; Bonazzoli E; Zammataro L; Yao X; Deshpande A; Zaidi S; Guglielmi A; Gnutti B; Nagarkatti N; Tymon-Rosario JR; Harold J; Mauricio D; Zeybek B; Menderes G; Altwerger G; Jeong K; Zhao S; Buza N; Hui P; Ravaggi A; Bignotti E; Romani C; Todeschini P; Zanotti L; Odicino F; Pecorelli S; Ardighieri L; Bilguvar K; Quick CM; Silasi DA; Huang GS; Andikyan V; Clark M; Ratner E; Azodi M; Imielinski M; Schwartz PE; Alexandrov LB; Lifton RP; Schlessinger J; Santin AD
Proc Natl Acad Sci U S A; 2021 Apr; 118(15):. PubMed ID: 33876771
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4. Risk of second primary malignancies among patients with carcinoid of the lung.
Buikhuisen WA; Steinbusch LC; Kodach LL; Tesselaar MET; Damhuis RAM
Lung Cancer; 2021 Jan; 151():5-7. PubMed ID: 33278670
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5. A novel mutation of the men1 gene in a patient with multiple endocrine neoplasia type 1 and recurrent fibromyxoid sarcoma - a case report.
Radman M; Milicevic T
BMC Med Genet; 2020 Sep; 21(1):190. PubMed ID: 32993530
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6. Reconstruction of the pelvic ring in iliac or iliosacral resections: allograft or autograft?
Khal A; Zucchini R; Sambri A; Leucuta DC; Mariotti F; Donati DM; De Paolis M
Musculoskelet Surg; 2022 Mar; 106(1):21-27. PubMed ID: 32390095
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7. Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
Mirabello L; Zhu B; Koster R; Karlins E; Dean M; Yeager M; Gianferante M; Spector LG; Morton LM; Karyadi D; Robison LL; Armstrong GT; Bhatia S; Song L; Pankratz N; Pinheiro M; Gastier-Foster JM; Gorlick R; de Toledo SRC; Petrilli AS; Patino-Garcia A; Lecanda F; Gutierrez-Jimeno M; Serra M; Hattinger C; Picci P; Scotlandi K; Flanagan AM; Tirabosco R; Amary MF; Kurucu N; Ilhan IE; Ballinger ML; Thomas DM; Barkauskas DA; Mejia-Baltodano G; Valverde P; Hicks BD; Zhu B; Wang M; Hutchinson AA; Tucker M; Sampson J; Landi MT; Freedman ND; Gapstur S; Carter B; Hoover RN; Chanock SJ; Savage SA
JAMA Oncol; 2020 May; 6(5):724-734. PubMed ID: 32191290
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8. Next-generation sequencing analysis identifies genomic alterations in pathological morphologies: A case of pulmonary carcinosarcoma harboring EGFR mutations.
Koba H; Kimura H; Nishikawa S; Sone T; Abo M; Hara J; Hosomichi K; Tajima A; Kasahara K
Lung Cancer; 2018 Aug; 122():146-150. PubMed ID: 30032823
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9. Hibernoma Mimicking Atypical Lipomatous Tumor: 64 Cases of a Morphologically Distinct Subset.
Al Hmada Y; Schaefer IM; Fletcher CDM
Am J Surg Pathol; 2018 Jul; 42(7):951-957. PubMed ID: 29629919
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10. Loss of the tumour suppressor gene AIP mediates the browning of human brown fat tumours.
Magnusson L; Hansen N; Saba KH; Nilsson J; Fioretos T; Rissler P; Nord KH
J Pathol; 2017 Oct; 243(2):160-164. PubMed ID: 28722204
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11. Genome-Wide Analysis Identifies men1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST.
Pantaleo MA; Urbini M; Indio V; Ravegnini G; Nannini M; De Luca M; Tarantino G; Angelini S; Gronchi A; Vincenzi B; Grignani G; Colombo C; Fumagalli E; Gatto L; Saponara M; Ianni M; Paterini P; Santini D; Pirini MG; Ceccarelli C; Altimari A; Gruppioni E; Renne SL; Collini P; Stacchiotti S; Brandi G; Casali PG; Pinna AD; Astolfi A; Biasco G
Mol Cancer Res; 2017 May; 15(5):553-562. PubMed ID: 28130400
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12. Somatic IDH1 mutation in a pituitary adenoma of a patient with Maffucci syndrome.
Hao S; Hong CS; Feng J; Yang C; Chittiboina P; Zhang J; Zhuang Z
J Neurosurg; 2016 Jun; 124(6):1562-7. PubMed ID: 26473790
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13. MicroRNA-142-3p, a novel target of tumor suppressor menin, inhibits osteosarcoma cell proliferation by down-regulation of FASN.
Yang YQ; Qi J; Xu JQ; Hao P
Tumour Biol; 2014 Oct; 35(10):10287-93. PubMed ID: 25034529
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14. Somatostatin receptors: from signaling to clinical practice.
Theodoropoulou M; Stalla GK
Front Neuroendocrinol; 2013 Aug; 34(3):228-52. PubMed ID: 23872332
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15. A genome-wide approach to comparative oncology: high-resolution oligonucleotide aCGH of canine and human osteosarcoma pinpoints shared microaberrations.
Angstadt AY; Thayanithy V; Subramanian S; Modiano JF; Breen M
Cancer Genet; 2012 Nov; 205(11):572-87. PubMed ID: 23137772
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16. Multiple endocrine neoplasia type 1 with unusual concomitance of various neoplastic disorders.
Nishimura Y; Yamashita K; Yumita W; Yamazaki M; Katai M; Sakurai A; Hashizume K
Endocr J; 2004 Feb; 51(1):75-81. PubMed ID: 15004412
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17. Sinonasal smooth muscle cell tumors: a clinicopathologic and immunohistochemical analysis of 12 cases with emphasis on the low-grade end of the spectrum.
Huang HY; Antonescu CR
Arch Pathol Lab Med; 2003 Mar; 127(3):297-304. PubMed ID: 12653572
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18. Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics.
Gisselsson D; Domanski HA; Höglund M; Carlén B; Mertens F; Willén H; Mandahl N
Am J Surg Pathol; 1999 Oct; 23(10):1300-4. PubMed ID: 10524534
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19. Assignment of the human FAU gene to a subregion of chromosome 11q13.
Kas K; Schoenmakers E; van de Ven W; Weber G; Nordenskjöld M; Michiels L; Merregaert J; Larsson C
Genomics; 1993 Aug; 17(2):387-92. PubMed ID: 8406491
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20. Exclusion of FAU as the multiple endocrine neoplasia type 1 (men1) gene.
Kas K; Weber G; Merregaert J; Michiels L; Sandelin K; Skogseid B; Thompson N; Nordenskjöld M; Larsson C; Friedman E
Hum Mol Genet; 1993 Apr; 2(4):349-53. PubMed ID: 8099302
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