Search Results - "WAINWRIGHT, Luanne M"

Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors by Eaton, Katherine W., Tooke, Laura S., Wainwright, Luanne M., Judkins, Alexander R., Biegel, Jaclyn A.

“…Background Germline mutations and deletions of SMARCB1/INI1 in chromosome band 22q11.2 predispose patients to rhabdoid tumor and schwannomatosis. Previous…”
Get full text

Mutation of the INI1 gene in composite rhabdoid tumor of the endometrium by Donner, Ludvik R., MD, PhD, Wainwright, Luanne M., BSMT, Zhang, Fan, PhD, Biegel, Jaclyn A., PhD

“…Summary Composite rhabdoid tumors are typically adult tumors that contain a component of rhabdoid cells, which are characteristic of the aggressive childhood…”
Get full text

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors by Biegel, J A, Zhou, J Y, Rorke, L B, Stenstrom, C, Wainwright, L M, Fogelgren, B

“…We examined 18 atypical teratoid and rhabdoid tumors of the brain and 7 renal and 4 extrarenal rhabdoid tumors for mutations in the candidate rhabdoid tumor…”
Get full text

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor by JACKSON, Eric M, SHAIKH, Tamim H, GURURANGAN, Sridharan, JONES, Marilyn C, MALKIN, David, NIKKEL, Sarah M, ZUPPAN, Craig W, WAINWRIGHT, Luanne M, FAN ZHANG, BIEGEL, Jaclyn A

“…Malignant rhabdoid tumors are highly aggressive neoplasms found primarily in infants and young children. The majority of rhabdoid tumors arise as a result of…”
Get full text

ALK Expression in Rhabdomyosarcomas: Correlation with Histologic Subtype and Fusion Status by Corao, Diana A., Biegel, Jaclyn A., Coffin, Cheryl M., Barr, Frederic G., Wainwright, Luanne M., Ernst, Linda M., Choi, John K., Zhang, Paul J., Pawel, Bruce R.

“…Immunohistochemical staining for anaplastic lymphoma kinase (ALK) has been described in rhabdomyosarcomas (RMS), especially the alveolar subtype. Previous…”
Get full text

Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors by Dougherty, Margaret J, Tooke, Laura S, Sullivan, Lisa M, Hakonarson, Hakon, Wainwright, Luanne M, Biegel, Jaclyn A

“…High-resolution single nucleotide polymorphism (SNP) arrays have been effectively implemented as a first tier test in clinical cytogenetics laboratories for…”
Get full text

Atypical teratoid/rhabdoid tumor in a patient with Beckwith–Wiedemann syndrome by Jackson, Eric M., Shaikh, Tamim H., Zhang, Fan, Wainwright, Luanne M., Storm, Phillip B., Hakonarson, Hakon, Zackai, Elaine H., Biegel, Jaclyn A.

“…Beckwith–Wiedemann syndrome (BWS) is a genetic disorder associated with an increased risk of childhood tumors. Here we describe a patient with BWS who…”
Get full text

No evidence for hypermethylation of the hSNF5/INI1 promoter in pediatric rhabdoid tumors by Zhang, Fan, Tan, Lu, Wainwright, Luanne M., Bartolomei, Marisa S., Biegel, Jaclyn A.

“…The hSNF5/INI1 gene on chromosome 22 has been implicated as a tumor suppressor gene in pediatric rhabdoid tumor, an aggressive malignancy that generally occurs…”
Get full text

GermlineINI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor by Biegel, Jaclyn A., Fogelgren, Benjamin, Wainwright, Luanne M., Zhou, Jun-Ying, Bevan, Herbert, Rorke, Lucy B.

Get full text

Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor by Biegel, Jaclyn A., Fogelgren, Benjamin, Wainwright, Luanne M., Zhou, Jun-Ying, Bevan, Herbert, Rorke, Lucy B.

“…We describe a four‐month‐old child who presented with an atypical teratoid/rhabdoid tumor of the brain and subsequently developed a renal rhabdoid tumor…”
Get full text

Atypical teratoid/rhabdoid tumor in a patient with Beckwith-Wiedemann syndrome by Jackson, Eric M., Shaikh, Tamim H., Zhang, Fan, Wainwright, Luanne M., Storm, Phillip B., Hakonarson, Hakon, Zackai, Elaine H., Biegel, Jaclyn A.

Get full text