Terms: = Brain cancer AND PAX7, PAX7B, 5081, ENSG00000009709, P23759, HUP1
10 results:
1. Inflammatory Rhabdomyoblastic Tumor: Clinicopathologic and Molecular Analysis of 13 Cases.
Odate T; Satomi K; Kubo T; Matsushita Y; Ueno T; Kurose A; Shomori K; Nakai T; Watanabe R; Segawa K; Ohshika S; Miyake N; Kudo S; Shimoi T; Kobayashi E; Komiyama M; Yoshimoto S; Nakatani F; Kawai A; Yatabe Y; Kohsaka S; Ichimura K; Ichikawa H; Yoshida A
Mod Pathol; 2024 Jan; 37(1):100359. PubMed ID: 37871654
[TBL] [Abstract] [Full Text] [Related]
2. Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.
van den Heuvel A; Lassche S; Mul K; Greco A; San León Granado D; Heerschap A; Küsters B; Tapscott SJ; Voermans NC; van Engelen BGM; van der Maarel SM
Sci Rep; 2022 Jan; 12(1):1426. PubMed ID: 35082321
[TBL] [Abstract] [Full Text] [Related]
3. An autopsy case of prostatic rhabdomyosarcoma with DICER1 hotspot mutation.
Miyama Y; Makise N; Miyakawa J; Kume H; Fukayama M; Ushiku T
Pathol Int; 2021 Jan; 71(1):102-108. PubMed ID: 33112496
[TBL] [Abstract] [Full Text] [Related]
4. MECHANISMS IN ENDOCRINOLOGY: Pioneer transcription factors in pituitary development and tumorigenesis.
Harris J; Gouhier A; Drouin J
Eur J Endocrinol; 2021 Jan; 184(1):R1-R15. PubMed ID: 33112269
[TBL] [Abstract] [Full Text] [Related]
5. Evaluation of blood gene expression levels in facioscapulohumeral muscular dystrophy patients.
Signorelli M; Mason AG; Mul K; Evangelista T; Mei H; Voermans N; Tapscott SJ; Tsonaka R; van Engelen BGM; van der Maarel SM; Spitali P
Sci Rep; 2020 Oct; 10(1):17547. PubMed ID: 33067535
[TBL] [Abstract] [Full Text] [Related]
6. miR-206 family is important for mitochondrial and muscle function, but not essential for myogenesis in vitro.
Przanowska RK; Sobierajska E; Su Z; Jensen K; Przanowski P; Nagdas S; Kashatus JA; Kashatus DF; Bhatnagar S; Lukens JR; Dutta A
FASEB J; 2020 Jun; 34(6):7687-7702. PubMed ID: 32277852
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7. Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
Busse TM; Roth JJ; Wilmoth D; Wainwright L; Tooke L; Biegel JA
Genes Chromosomes Cancer; 2017 Oct; 56(10):730-749. PubMed ID: 28597942
[TBL] [Abstract] [Full Text] [Related]
8. PTEN deficiency reprogrammes human neural stem cells towards a glioblastoma stem cell-like phenotype.
Duan S; Yuan G; Liu X; Ren R; Li J; Zhang W; Wu J; Xu X; Fu L; Li Y; Yang J; Zhang W; Bai R; Yi F; Suzuki K; Gao H; Esteban CR; Zhang C; Izpisua Belmonte JC; Chen Z; Wang X; Jiang T; Qu J; Tang F; Liu GH
Nat Commun; 2015 Dec; 6():10068. PubMed ID: 26632666
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9. Rapidly progressive congenital rhabdomyosarcoma presenting with multiple cutaneous lesions: an uncommon diagnosis and a therapeutic challenge.
Rekhi B; Qureshi SS; Narula G; Gujral S; Kurkure P
Pathol Res Pract; 2014 May; 210(5):328-33. PubMed ID: 24635971
[TBL] [Abstract] [Full Text] [Related]
10. Bortezomib reverses a post-translational mechanism of tumorigenesis for patched1 haploinsufficiency in medulloblastoma.
Taniguchi E; Cho MJ; Arenkiel BR; Hansen MS; Rivera OJ; McCleish AT; Qualman SJ; Guttridge DC; Scott MP; Capecchi MR; Keller C
Pediatr Blood Cancer; 2009 Aug; 53(2):136-44. PubMed ID: 19213072
[TBL] [Abstract] [Full Text] [Related]
