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Hereditary intraspinal schwannomatosis with SMARCB1 gene mutation: A case report.

• Authors : Li Y; Department of Neurosurgery, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.; Chen L

Subjects: Neurilemmoma*/Neurilemmoma*/Neurilemmoma*/diagnostic imaging ; Neurilemmoma*/Neurilemmoma*/Neurilemmoma*/genetics ; Neurilemmoma*/Neurilemmoma*/Neurilemmoma*/pathology Schwannomatosis

• Source: Journal of clinical laboratory analysis [J Clin Lab Anal] 2022 Jun; Vol. 36 (6), pp. e24448. Date of Electronic Publication: 2022 Apr 21.Publisher: Wiley Country of Publication: United States NLM ID: 8801384 Publication Model: Print-Electronic Cited Medium:

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SMARCB1(INI1)‐deficient sinonasal adenocarcinoma: Report of a case previously diagnosed as high‐grade non‐intestinal‐type sinonasal adenocarcinoma

• Authors : Min-Shu Hsieh; Yu-Ju Su; Yi-Hsuan Lee

Subjects: Pathology; medicine.medical_specialty; business.industry

• Source: Pathology International. 72:53-58

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Loss of ARID1B and SMARCB1 expression are specific for the diagnosis of dedifferentiated/undifferentiated carcinoma in tumours of the upper gynaecological tract and cervix

• Authors : Cheng-Han Lee; Máire A. Duggan; Colin J.R. Stewart

Subjects: 0301 basic medicine; Pathology; medicine.medical_specialty

• Source: Histopathology. 79:160-167

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A case of desmoplastic myxoid tumor, SMARCB1 mutant, in the pineal region

• Authors : An-Li Zhang; Hai-Bo Wu; Wenchao Zhou

Subjects: Pathology; medicine.medical_specialty; Germinoma

• Source: Neuropathology. 41:37-41

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SMARCB1/ INI1‐deficient intrathoracic neoplasm with rhabdoid/plasmacytoid cytomorphology in a patient with plasma cell myeloma: A case report

• Authors : Fujita, Kazuki; Mizuguchi, Keishi; Mori, Tatsuya

• Source: Diagnostic Cytopathology ; volume 51, issue 10 ; ISSN 8755-1039 1097-0339

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SMARCB1 ( INI1)‐deficient sinonasal carcinoma manifesting as oral lesions: A report of two cases

• Authors : Fuoco, Jessie; Huang, Michelle; Esfandiari, Najmeh

• Source: Head & Neck ; volume 46, issue 3 ; ISSN 1043-3074 1097-0347

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Switch/sucrose‐non‐fermentable ( SWI / SNF ) complex ( SMARCA4 , SMARCA2 , INI1 / SMARCB1 )‐deficient colorectal carcinomas are strongly associated with microsatellite instability: an incidence study in 4508 colorectal carcinomas

• Authors : Mahsa S Ahadi; Talia L Fuchs; Adele Clarkson

Subjects: Histology; General Medicine; Pathology and Forensic Medicine

• Source: Histopathology. 80:906-921

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Use of clinical next-generation sequencing to identify melanomas harboring SMARCB1 mutations.

• Authors : Stockman DL; Department of Pathology and Laboratory Medicine, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.; Curry JL

Subjects: Mutation*; Chromosomal Proteins, Non-Histone/Chromosomal Proteins, Non-Histone/Chromosomal Proteins, Non-Histone/*genetics ; DNA-Binding Proteins/DNA-Binding Proteins/DNA-Binding Proteins/*genetics

• Source: Journal of cutaneous pathology [J Cutan Pathol] 2015 May; Vol. 42 (5), pp. 308-17. Date of Electronic Publication: 2015 Mar 24.Publisher: Wiley Country of Publication: United States NLM ID: 0425124 Publication Model: Print-Electronic Cited Medium:

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Loss of SMARCB1 promotes autophagy and facilitates tumour progression in chordoma by transcriptionally activating ATG5

• Authors : Li, Mingxuan; Shen, Yutao; Xiong, Yujia ...

• Source: Cell Proliferation ; volume 54, issue 12 ; ISSN 0960-7722 1365-2184

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Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors

• Authors : Sabatella, Mariangela; Mantere, Tuomo; Waanders, Esmé ...

• Source: The Journal of Pathology ; volume 255, issue 2, page 202-211 ; ISSN 0022-3417 1096-9896

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