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Histopathology, ISSN 0309-0167, 09/2018, Volume 73, Issue 3, pp. 438 - 443
The most common BRAF mutation in ovarian low-grade serous neoplasms (LGSNs) involves substitution of valine by glutamic acid at position 600 (V600E). Small... 
low‐grade serous carcinoma | mutation | ovary | 1 immunohistochemistry | 600E | BRAF | serous borderline tumour | Immunohistochemistry | Monoclonal antibodies | Genetic aspects | Metastasis | Gene mutations | Glutamate | Proteins | Glutamic acid | Carcinoma | Valine | Mutation | Paraffin | Metastases | Tumors | VE1 immunohistochemistry | BRAFV600E mutation | low-grade serous carcinoma
Journal Article
Human Pathology, ISSN 0046-8177, 06/2019, Volume 88, pp. 87 - 91
As immune checkpoint inhibitors are rapidly developing into the standard of care for patients with advanced melanoma, the value of diagnostic metrics to... 
PD-L1 | PD-L2 | 9p24.1 amplification | JAK2 | Immunotherapy | Melanoma | LYMPHOMA | PATHOLOGY | NIVOLUMAB | BLOCKADE | EXPRESSION | Metastasis | Drug therapy | Genes | Genomes | FDA approval | Patients | Proteins | Lymphocytes | Response rates | Biomarkers | Ligands | Lymphomas | Mutation | Signatures | Tumors
Journal Article
by Zehir, Ahmet and Benayed, Ryma and Shah, Ronak H and Syed, Aijazuddin and Middha, Sumit and Kim, Hyunjae R and Srinivasan, Preethi and Gao, Jianjiong and Chakravarty, Debyani and Devlin, Sean M and Hellmann, Matthew D and Barron, David A and Schram, Alison M and Hameed, Meera and Dogan, Snjezana and Ross, Dara S and Hechtman, Jaclyn F and DeLair, Deborah F and Yao, JinJuan and Mandelker, Diana L and Cheng, Donavan T and Chandramohan, Raghu and Mohanty, Abhinita S and Ptashkin, Ryan N and Jayakumaran, Gowtham and Prasad, Meera and Syed, Mustafa H and Rema, Anoop Balakrishnan and Liu, Zhen Y and Nafa, Khedoudja and Borsu, Laetitia and Sadowska, Justyna and Casanova, Jacklyn and Bacares, Ruben and Kiecka, Iwona J and Razumova, Anna and Son, Julie B and Stewart, Lisa and Baldi, Tessara and Mullaney, Kerry A and Al-Ahmadie, Hikmat and Vakiani, Efsevia and Abeshouse, Adam A and Penson, Alexander V and Jonsson, Philip and Camacho, Niedzica and Chang, Matthew T and Won, Helen H and Gross, Benjamin E and Kundra, Ritika and Heins, Zachary J and Chen, Hsiao-Wei and Phillips, Sarah and Zhang, Hongxin and Wang, Jiaojiao and Ochoa, Angelica and Wills, Jonathan and Eubank, Michael and Thomas, Stacy B and Gardos, Stuart M and Reales, Dalicia N and Galle, Jesse and Durany, Robert and Cambria, Roy and Abida, Wassim and Cercek, Andrea and Feldman, Darren R and Gounder, Mrinal M and Hakimi, A. Ari and Harding, James J and Iyer, Gopa and Janjigian, Yelena Y and Jordan, Emmet J and Kelly, Ciara M and Lowery, Maeve A and Morris, Luc G. T and Omuro, Antonio M and Raj, Nitya and Razavi, Pedram and Shoushtari, Alexander N and Shukla, Neerav and Soumerai, Tara E and Varghese, Anna M and Yaeger, Rona and Coleman, Jonathan and Bochner, Bernard and Riely, Gregory J and Saltz, Leonard B and Scher, Howard I and Sabbatini, Paul J and Robson, Mark E and Klimstra, David S and Taylor, Barry S and Baselga, Jose and Schultz, Nikolaus and Hyman, David M and Arcila, Maria E and Solit, David B and Ladanyi, Marc and Berger, Michael F
Nature Medicine, ISSN 1078-8956, 06/2017, Volume 23, Issue 6, pp. 703 - 713
Journal Article
Surgical Pathology Clinics, ISSN 1875-9181, 06/2016, Volume 9, Issue 2, pp. 269 - 287
This review covers gynecologic manifestations that may occur in rare hereditary syndromes. Recent advances in disorders, such as hereditary leiomyomatosis,... 
Cowden syndrome | Maffucci syndrome | Hereditary leiomyomatosis renal cell carcinoma syndrome | Tuberous sclerosis | Von Hippel-Lindau | Ollier disease | Carney complex | Nevoid basal cell carcinoma syndrome | Neoplastic Syndromes, Hereditary - pathology | Prognosis | Uterine Neoplasms - pathology | Humans | Lymphangioleiomyomatosis - pathology | Carney Complex - pathology | von Hippel-Lindau Disease - diagnosis | Genital Neoplasms, Female - diagnosis | Tuberous Sclerosis - pathology | Basal Cell Nevus Syndrome - pathology | von Hippel-Lindau Disease - pathology | Leiomyomatosis - diagnosis | Skin Neoplasms - diagnosis | Carney Complex - genetics | Leiomyomatosis - pathology | Female | Neoplastic Syndromes, Hereditary - genetics | Tuberous Sclerosis - diagnosis | Uterine Neoplasms - diagnosis | Carney Complex - diagnosis | Genital Neoplasms, Female - genetics | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Diagnosis, Differential | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Basal Cell Nevus Syndrome - diagnosis | Neoplastic Syndromes, Hereditary - diagnosis | von Hippel-Lindau Disease - genetics | Enchondromatosis - diagnosis | Tuberous Sclerosis - genetics | Perivascular Epithelioid Cell Neoplasms - pathology | Hamartoma Syndrome, Multiple - diagnosis | Perivascular Epithelioid Cell Neoplasms - genetics | Skin Neoplasms - genetics | Basal Cell Nevus Syndrome - genetics | Enchondromatosis - pathology | Leiomyomatosis - genetics | Perivascular Epithelioid Cell Neoplasms - diagnosis | Genital Neoplasms, Female - pathology | Enchondromatosis - genetics | Lymphangioleiomyomatosis - diagnosis | Lymphangioleiomyomatosis - genetics
Journal Article
The Journal of Pathology, ISSN 0022-3417, 10/2017, Volume 243, Issue 2, pp. 230 - 241
Journal Article
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 01/2017, Volume 41, Issue 1, pp. 12 - 24
Journal Article
Histopathology, ISSN 0309-0167, 09/2018, Volume 73, Issue 3, pp. 438 - 443
Journal Article
Journal Article
JNCCN Journal of the National Comprehensive Cancer Network, ISSN 1540-1405, 02/2018, Volume 16, Issue 2, pp. 201 - 209
Endometrial cancers are the most common gynecologic malignancies. The staging of endometrial cancer has evolved from a clinical-based system to a comprehensive... 
FIGO GRADE | REPAIR PROTEIN EXPRESSION | RISK-FACTORS | ONCOLOGY | IMMUNOHISTOCHEMICAL ANALYSIS | MICROSATELLITE INSTABILITY | TUMOR MORPHOLOGY | UTERINE CORPUS | LOW-GRADE | UNDIFFERENTIATED CARCINOMA | CLINICOPATHOLOGICAL ANALYSIS
Journal Article
The Journal of Pathology, ISSN 0022-3417, 10/2017, Volume 243, Issue 2, pp. 230 - 241
Journal Article