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Recurrent EML4–NTRK3 fusions in infantile fibrosarcoma and congenital mesoblastic nephroma suggest a revised testing strategy
by
Skalova, Alena
, Gomez-Fernandez, Carmen R
, Perez-Atayde, Antonio R
, Dela Cruz, Filemon S
, Glade-Bender, Julia L
, Tannenbaum-Dvir, Sarah
, Kung, Andrew L
, Janeway, Katherine A
, Stahl, Joshua A
, Calicchio, Monica L
, Dillon, Deborah A
, Kozakewich, Harry P
, Haimes, Josh D
, Church, Alanna J
, Nardi, Valentina
, Harris, Marian H
, DuBois, Steven G
, Manoj, Namitha
, Pinto, Andre
in
45/91
/ 631/67/2332
/ 692/308/2056
/ Adolescent
/ Adult
/ Aged
/ Aged, 80 and over
/ Breast cancer
/ Breast carcinoma
/ Breast Neoplasms - genetics
/ Carcinoma - genetics
/ Case reports
/ Cell Cycle Proteins - genetics
/ Child, Preschool
/ Discoidin Domain Receptor 2 - genetics
/ ETS Translocation Variant 6 Protein
/ Female
/ Fibrosarcoma
/ Fibrosarcoma - diagnosis
/ Fibrosarcoma - genetics
/ Gene fusion
/ Genetic Testing
/ Humans
/ In Situ Hybridization, Fluorescence
/ Infant
/ Infant, Newborn
/ Kidney Neoplasms - congenital
/ Kidney Neoplasms - diagnosis
/ Kidney Neoplasms - genetics
/ Laboratory Medicine
/ Male
/ Medicine
/ Medicine & Public Health
/ Microtubule-Associated Proteins - genetics
/ Middle Aged
/ Neoplasm Recurrence, Local - genetics
/ Nephroma, Mesoblastic - congenital
/ Nephroma, Mesoblastic - diagnosis
/ Nephroma, Mesoblastic - genetics
/ NTRK3 gene
/ Oncogene Proteins, Fusion - genetics
/ original-article
/ Pathology
/ Proto-Oncogene Proteins c-ets - genetics
/ Repressor Proteins - genetics
/ Ribonucleic acid
/ RNA
/ Sequence Analysis, RNA
/ Serine Endopeptidases - genetics
/ Tumors
2018
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Recurrent EML4–NTRK3 fusions in infantile fibrosarcoma and congenital mesoblastic nephroma suggest a revised testing strategy
by
Skalova, Alena
, Gomez-Fernandez, Carmen R
, Perez-Atayde, Antonio R
, Dela Cruz, Filemon S
, Glade-Bender, Julia L
, Tannenbaum-Dvir, Sarah
, Kung, Andrew L
, Janeway, Katherine A
, Stahl, Joshua A
, Calicchio, Monica L
, Dillon, Deborah A
, Kozakewich, Harry P
, Haimes, Josh D
, Church, Alanna J
, Nardi, Valentina
, Harris, Marian H
, DuBois, Steven G
, Manoj, Namitha
, Pinto, Andre
in
45/91
/ 631/67/2332
/ 692/308/2056
/ Adolescent
/ Adult
/ Aged
/ Aged, 80 and over
/ Breast cancer
/ Breast carcinoma
/ Breast Neoplasms - genetics
/ Carcinoma - genetics
/ Case reports
/ Cell Cycle Proteins - genetics
/ Child, Preschool
/ Discoidin Domain Receptor 2 - genetics
/ ETS Translocation Variant 6 Protein
/ Female
/ Fibrosarcoma
/ Fibrosarcoma - diagnosis
/ Fibrosarcoma - genetics
/ Gene fusion
/ Genetic Testing
/ Humans
/ In Situ Hybridization, Fluorescence
/ Infant
/ Infant, Newborn
/ Kidney Neoplasms - congenital
/ Kidney Neoplasms - diagnosis
/ Kidney Neoplasms - genetics
/ Laboratory Medicine
/ Male
/ Medicine
/ Medicine & Public Health
/ Microtubule-Associated Proteins - genetics
/ Middle Aged
/ Neoplasm Recurrence, Local - genetics
/ Nephroma, Mesoblastic - congenital
/ Nephroma, Mesoblastic - diagnosis
/ Nephroma, Mesoblastic - genetics
/ NTRK3 gene
/ Oncogene Proteins, Fusion - genetics
/ original-article
/ Pathology
/ Proto-Oncogene Proteins c-ets - genetics
/ Repressor Proteins - genetics
/ Ribonucleic acid
/ RNA
/ Sequence Analysis, RNA
/ Serine Endopeptidases - genetics
/ Tumors
2018
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Recurrent EML4–NTRK3 fusions in infantile fibrosarcoma and congenital mesoblastic nephroma suggest a revised testing strategy
by
Skalova, Alena
, Gomez-Fernandez, Carmen R
, Perez-Atayde, Antonio R
, Dela Cruz, Filemon S
, Glade-Bender, Julia L
, Tannenbaum-Dvir, Sarah
, Kung, Andrew L
, Janeway, Katherine A
, Stahl, Joshua A
, Calicchio, Monica L
, Dillon, Deborah A
, Kozakewich, Harry P
, Haimes, Josh D
, Church, Alanna J
, Nardi, Valentina
, Harris, Marian H
, DuBois, Steven G
, Manoj, Namitha
, Pinto, Andre
in
45/91
/ 631/67/2332
/ 692/308/2056
/ Adolescent
/ Adult
/ Aged
/ Aged, 80 and over
/ Breast cancer
/ Breast carcinoma
/ Breast Neoplasms - genetics
/ Carcinoma - genetics
/ Case reports
/ Cell Cycle Proteins - genetics
/ Child, Preschool
/ Discoidin Domain Receptor 2 - genetics
/ ETS Translocation Variant 6 Protein
/ Female
/ Fibrosarcoma
/ Fibrosarcoma - diagnosis
/ Fibrosarcoma - genetics
/ Gene fusion
/ Genetic Testing
/ Humans
/ In Situ Hybridization, Fluorescence
/ Infant
/ Infant, Newborn
/ Kidney Neoplasms - congenital
/ Kidney Neoplasms - diagnosis
/ Kidney Neoplasms - genetics
/ Laboratory Medicine
/ Male
/ Medicine
/ Medicine & Public Health
/ Microtubule-Associated Proteins - genetics
/ Middle Aged
/ Neoplasm Recurrence, Local - genetics
/ Nephroma, Mesoblastic - congenital
/ Nephroma, Mesoblastic - diagnosis
/ Nephroma, Mesoblastic - genetics
/ NTRK3 gene
/ Oncogene Proteins, Fusion - genetics
/ original-article
/ Pathology
/ Proto-Oncogene Proteins c-ets - genetics
/ Repressor Proteins - genetics
/ Ribonucleic acid
/ RNA
/ Sequence Analysis, RNA
/ Serine Endopeptidases - genetics
/ Tumors
2018
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Recurrent EML4–NTRK3 fusions in infantile fibrosarcoma and congenital mesoblastic nephroma suggest a revised testing strategy
Journal Article
Recurrent EML4–NTRK3 fusions in infantile fibrosarcoma and congenital mesoblastic nephroma suggest a revised testing strategy
2018
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Overview
Infantile fibrosarcoma and congenital mesoblastic nephroma are tumors of infancy traditionally associated with the
ETV6–NTRK3
gene fusion. However, a number of case reports have identified variant fusions in these tumors. In order to assess the frequency of variant
NTRK3
fusions, and in particular whether the recently identified
EML4–NTRK3
fusion is recurrent, 63 archival cases of infantile fibrosarcoma, congenital mesoblastic nephroma, mammary analog secretory carcinoma and secretory breast carcinoma (tumor types that are known to carry recurrent
ETV6–NTRK3
fusions) were tested with
NTRK3
break-apart FISH,
EML4–NTRK3
dual fusion FISH, and targeted RNA sequencing. The
EML4–NTRK3
fusion was identified in two cases of infantile fibrosarcoma (one of which was previously described), and in one case of congenital mesoblastic nephroma, demonstrating that the
EML4–NTRK3
fusion is a recurrent genetic event in these related tumors. The growing spectrum of gene fusions associated with infantile fibrosarcoma and congenital mesoblastic nephroma along with the recent availability of targeted therapies directed toward inhibition of NTRK signaling argue for alternate testing strategies beyond
ETV6
break-apart FISH. The use of either
NTRK3
FISH or next-generation sequencing will expand the number of cases in which an oncogenic fusion is identified and facilitate optimal diagnosis and treatment for patients.
Publisher
Nature Publishing Group US,Elsevier Limited
Subject
/ Adult
/ Aged
/ Cell Cycle Proteins - genetics
/ Discoidin Domain Receptor 2 - genetics
/ ETS Translocation Variant 6 Protein
/ Female
/ Humans
/ In Situ Hybridization, Fluorescence
/ Infant
/ Kidney Neoplasms - congenital
/ Kidney Neoplasms - diagnosis
/ Male
/ Medicine
/ Microtubule-Associated Proteins - genetics
/ Neoplasm Recurrence, Local - genetics
/ Nephroma, Mesoblastic - congenital
/ Nephroma, Mesoblastic - diagnosis
/ Nephroma, Mesoblastic - genetics
/ Oncogene Proteins, Fusion - genetics
/ Proto-Oncogene Proteins c-ets - genetics
/ Repressor Proteins - genetics
/ RNA
/ Serine Endopeptidases - genetics
/ Tumors
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