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STK11 Adnexal Tumor in an Adolescent Female: Diagnostic Pitfalls of a Recently Described Entity.
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- Pediatric & Developmental Pathology, 2023, v. 26, n. 5, p. 486, doi. 10.1177/10935266231176681
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- Article
Targeted genomic analysis of Müllerian adenosarcoma.
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- Journal of Pathology, 2015, v. 235, n. 1, p. 37, doi. 10.1002/path.4442
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- Article
Does the introduction of new technology change population demographics? Minimally invasive technologies and endometrial polyps.
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- 2002
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- Publication type:
- journal article
A spatially and temporally restricted mouse model of soft tissue sarcoma.
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- Nature Medicine, 2007, v. 13, n. 8, p. 992, doi. 10.1038/nm1602
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- Publication type:
- Article
Role of K-ras and Pten in the development of mouse models of endometriosis and endometrioid ovarian cancer.
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- Nature Medicine, 2005, v. 11, n. 1, p. 63, doi. 10.1038/nm1173
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- Article
Secretory cell outgrowth, PAX2 and serous carcinogenesis in the Fallopian tube.
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- Journal of Pathology, 2010, v. 222, n. 1, p. 110, doi. 10.1002/path.2739
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- Publication type:
- Article
The Li-Fraumeni syndrome (LFS): a model for the initiation of p53 signatures in the distal Fallopian tube.
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- Journal of Pathology, 2010, v. 220, n. 1, p. 17, doi. 10.1002/path.2624
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- Publication type:
- Article
The Role of CD10 Staining in Distinguishing Invasive Endometrial Adenocarcinoma from Adenocarcinoma Involving Adenomyosis.
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- Modern Pathology, 2003, v. 16, n. 1, p. 22, doi. 10.1097/01.MP.0000043523.03519.FC
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- Article
Intravenous Leiomyomatosis: Molecular and Cytogenetic Analysis of a Case.
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- Modern Pathology, 2002, v. 15, n. 3, p. 351, doi. 10.1038/modpathol.3880529
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- Publication type:
- Article
Expanding the spectrum of translocations in sclerosing epitheloid fibrosarcoma: A new case with EWSR1‐CREB3L3 fusion.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 675, doi. 10.1002/gcc.22677
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- Publication type:
- Article
Prenatal sonography in trisomy 9.
- Published in:
- 1992
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- Publication type:
- journal article
Peritoneal Dissemination Complicating Morcellation of Uterine Mesenchymal Neoplasms.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050058
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- Publication type:
- Article
Meningeal carcinomatosis from transitional cell carcinoma of the bladder.
- Published in:
- 1993
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- Publication type:
- journal article
Granulocyte Macrophage Colony-Stimulating Factor in Adenomyosis and Autologous Endometrium.
- Published in:
- Reproductive Sciences, 2002, v. 9, n. 2, p. 93, doi. 10.1177/107155760200900208
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- Publication type:
- Article
Dedifferentiated leiomyosarcoma of the uterus: a clinicopathologic and immunohistochemical analysis of 23 cases.
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- Histopathology, 2023, v. 82, n. 6, p. 812, doi. 10.1111/his.14870
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- Publication type:
- Article
Predictors of adverse outcome in uterine smooth muscle tumours of uncertain malignant potential (STUMP): a clinicopathological analysis of 22 cases with a proposal for the inclusion of additional histological parameters.
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- Histopathology, 2018, v. 73, n. 2, p. 284, doi. 10.1111/his.13515
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- Publication type:
- Article
Abnormal p53 and p16 staining patterns distinguish uterine leiomyosarcoma from inflammatory myofibroblastic tumour.
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- Histopathology, 2017, v. 70, n. 7, p. 1138, doi. 10.1111/his.13176
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- Publication type:
- Article
Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profiling of the t(12;14) and evidence in support of predisposing genetic heterogeneity.
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- Human Molecular Genetics, 2012, v. 21, n. 10, p. 2312, doi. 10.1093/hmg/dds051
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- Publication type:
- Article
Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 12, p. 1152, doi. 10.1002/gcc.20824
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- Publication type:
- Article
Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis.
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- Genes, Chromosomes & Cancer, 2009, v. 48, n. 10, p. 865, doi. 10.1002/gcc.20692
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- Publication type:
- Article
Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 3, p. 304, doi. 10.1002/gcc.20291
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- Publication type:
- Article
Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 2, p. 97, doi. 10.1002/gcc.20018
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- Publication type:
- Article
Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24).
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- Genes, Chromosomes & Cancer, 2003, v. 36, n. 2, p. 205, doi. 10.1002/gcc.10159
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- Publication type:
- Article
Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva.
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- Genes, Chromosomes & Cancer, 2001, v. 32, n. 2, p. 172, doi. 10.1002/gcc.1179
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- Publication type:
- Article
Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 209, doi. 10.1002/(SICI)1098-2264(200002)27:2<209::AID-GCC14>3.0.CO;2-U
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- Article
Primary Parauterine Leiomyoma With a t(6;14).
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 385, doi. 10.1002/(SICI)1098-2264(199912)26:4<385::AID-GCC15>3.0.CO;2-G
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- Publication type:
- Article
HMGIC expression in human adult and fetal tissues and in uterine leiomyomata.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 4, p. 316, doi. 10.1002/(SICI)1098-2264(199908)25:4<316::AID-GCC2>3.0.CO;2-0
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- Publication type:
- Article
Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 4, p. 361, doi. 10.1002/(SICI)1098-2264(199812)23:4<361::AID-GCC12>3.0.CO;2-4
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- Publication type:
- Article
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-40037-4
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- Publication type:
- Article
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-40037-4
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- Publication type:
- Article