48,452
edits
Difference between revisions of "SMARCB1"
Jump to navigation
Jump to search
→Negative
| (One intermediate revision by the same user not shown) | |||
| Line 17: | Line 17: | ||
'''SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily B, member 1''', commonly abbreviated '''SMARCB1''', is a diagnostic [[immunostain]], because nuclear staining is lost in some specific types of cancer shown below. | '''SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily B, member 1''', commonly abbreviated '''SMARCB1''', is a diagnostic [[immunostain]], because nuclear staining is lost in some specific types of cancer shown below. | ||
It is also known as '''INI1''' and '''BAF47'''. | It is also known as '''INI1''', '''INI-1''' and '''BAF47'''. | ||
==Negative== | ==Negative== | ||
| Line 26: | Line 26: | ||
* [[Atypical teratoid/rhabdoid tumour]].<ref>{{Cite journal | last1 = Hasselblatt | first1 = M. | last2 = Isken | first2 = S. | last3 = Linge | first3 = A. | last4 = Eikmeier | first4 = K. | last5 = Jeibmann | first5 = A. | last6 = Oyen | first6 = F. | last7 = Nagel | first7 = I. | last8 = Richter | first8 = J. | last9 = Bartelheim | first9 = K. | title = High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors. | journal = Genes Chromosomes Cancer | volume = 52 | issue = 2 | pages = 185-90 | month = Feb | year = 2013 | doi = 10.1002/gcc.22018 | PMID = 23074045 }}</ref> | * [[Atypical teratoid/rhabdoid tumour]].<ref>{{Cite journal | last1 = Hasselblatt | first1 = M. | last2 = Isken | first2 = S. | last3 = Linge | first3 = A. | last4 = Eikmeier | first4 = K. | last5 = Jeibmann | first5 = A. | last6 = Oyen | first6 = F. | last7 = Nagel | first7 = I. | last8 = Richter | first8 = J. | last9 = Bartelheim | first9 = K. | title = High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors. | journal = Genes Chromosomes Cancer | volume = 52 | issue = 2 | pages = 185-90 | month = Feb | year = 2013 | doi = 10.1002/gcc.22018 | PMID = 23074045 }}</ref> | ||
* Up to 30% of [[synovial sarcoma]].<ref>{{Cite journal | last1 = Mularz | first1 = K. | last2 = Harazin-Lechowska | first2 = A. | last3 = Ambicka | first3 = A. | last4 = Kruczak | first4 = A. | last5 = Rozmus-Piętoń | first5 = M. | last6 = Marchińska-Osika | first6 = U. | last7 = Swiątkiewicz | first7 = I. | last8 = Król | first8 = M. | last9 = Pabis | first9 = D. | title = Specificity and sensitivity of INI-1 labeling in epithelioid sarcoma. Loss of INI1 expression as a frequent immunohistochemical event in synovial sarcoma. | journal = Pol J Pathol | volume = 63 | issue = 3 | pages = 179-83 | month = Nov | year = 2012 | doi = | PMID = 23161234 }}</ref> | * Up to 30% of [[synovial sarcoma]].<ref>{{Cite journal | last1 = Mularz | first1 = K. | last2 = Harazin-Lechowska | first2 = A. | last3 = Ambicka | first3 = A. | last4 = Kruczak | first4 = A. | last5 = Rozmus-Piętoń | first5 = M. | last6 = Marchińska-Osika | first6 = U. | last7 = Swiątkiewicz | first7 = I. | last8 = Król | first8 = M. | last9 = Pabis | first9 = D. | title = Specificity and sensitivity of INI-1 labeling in epithelioid sarcoma. Loss of INI1 expression as a frequent immunohistochemical event in synovial sarcoma. | journal = Pol J Pathol | volume = 63 | issue = 3 | pages = 179-83 | month = Nov | year = 2012 | doi = | PMID = 23161234 }}</ref> | ||
* [[Renal medullary carcinoma]]. | |||
==See also== | ==See also== | ||