An Xp11.2 translocation renal cell carcinoma with SMARCB1 (INI1) inactivation in adult end-stage renal disease: a case report

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An Xp11.2 translocation renal cell carcinoma with SMARCB1 (INI1) inactivation in adult end-stage renal disease: a case report

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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An Xp11.2 translocation renal ...... e renal disease: a case report

@en

An Xp11.2 translocation renal cell carcinoma with SMARCB1

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label

An Xp11.2 translocation renal ...... e renal disease: a case report

@en

An Xp11.2 translocation renal cell carcinoma with SMARCB1

@nl

prefLabel

An Xp11.2 translocation renal ...... e renal disease: a case report

@en

An Xp11.2 translocation renal cell carcinoma with SMARCB1

@nl

P1476

An Xp11.2 translocation renal ...... e renal disease: a case report

@en

P2093

Guoping Wang

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Jun Li

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Lu Yu

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Mariajose Navia Miranda

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Sanpeng Xu

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Yaqi Duan

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P2860

Therapeutically targeting cyclin D1 in primary tumors arising from loss of Ini1.

SMARCB1(INI1)-deficient sinonasal basaloid carcinoma: a novel member of the expanding family of SMARCB1-deficient neoplasms.

Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma.

Loss of INI1 expression defines a unique subset of pediatric undifferentiated soft tissue sarcomas.

The role of SMARCB1/INI1 in development of rhabdoid tumor.

The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia.

The expanding family of SMARCB1(INI1)-deficient neoplasia: implications of phenotypic, biological, and molecular heterogeneity.

Immunohistochemical analysis of SMARCB1/INI-1 expression in collecting duct carcinoma.

PSF/SFPQ is a very common gene fusion partner in TFE3 rearrangement-associated perivascular epithelioid cell tumors (PEComas) and melanotic Xp11 translocation renal cancers: clinicopathologic, immunohistochemical, and molecular characteristics sugge

Epithelioid malignant peripheral nerve sheath tumor: clinicopathologic analysis of 63 cases.

P2888

s13000-016-0551-x

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scholarly article

case report

P356

10.1186/S13000-016-0551-X

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P478

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2016-10-12T00:00:00Z

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1001061653

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27733182

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5062893

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