Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Patrick Bogard"'
Autor:
Tyler Landrith, Samantha Smith, Jennifer Chan, Mari Christensen, Yu Chuan Tai, Megan Gonzales, William Yee, Nicolas Newton, Wouter Pattje, Patrick Bogard, Wei Yang
Publikováno v:
Cancer Research. 83:6162-6162
The measurement of HER2 (ERBB2) gene amplification guides both the prognosis and treatment of breast cancer, as amplification correlates with worse outcomes and the recommendation for anti-HER2 treatment. Digital PCR (dPCR) can serve as a useful tool
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a6a33a5d7989ca0cb43945937e13595
https://doi.org/10.1158/1538-7445.am2023-6162
https://doi.org/10.1158/1538-7445.am2023-6162
Autor:
Renee P Stokowski, Ehsan Tabari, Patrick Bogard, Coleen Hacker, Olga K Kameneva, Tieming Ji, Li Teng, Vladislava Melnikova, Ron McCord, Elizabeth A Punnoose, Robert Loberg, Junaid Shabbeer
Publikováno v:
Blood. 140:9257-9258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c8857ac9d013ecff29d80736f277419
https://doi.org/10.1182/blood-2022-162814
https://doi.org/10.1182/blood-2022-162814
Autor:
Wei Yang, Mari Christensen, Jennifer K. Chan, Julie Tsai, Nancy Patten, Ha B. Tran, Grant R. Hillman, Yu Chuan Tai, Patrick Bogard, Claudia M. Litterst, Victoria H. Brophy, Nick Newton, Christopher D. Nelson, Wouter J. Pattje
Publikováno v:
Cancer Research. 82:5156-5156
Non-small cell lung cancer (NSCLC) patients harboring activating mutations in epidermal growth factor receptor (EGFR) are benefited from Tyrosine Kinase Inhibitor (TKI) targeted therapy. However, more than 50% of patients receiving the first or secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1df76bd403e928248f8c31dde0f7c5a
https://doi.org/10.1158/1538-7445.am2022-5156
https://doi.org/10.1158/1538-7445.am2022-5156
Publikováno v:
American Journal of Clinical Pathology. 83:236-240
The clinical and histologic features of a benign cystic teratoma with histologic evidence of almost full gastrointestinal tract development are discussed. The literature has previously described only bowel epithelium, segments of bowel, appendix, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91705218d4d0ccf37f79d0d57ed18c5
https://doi.org/10.1093/ajcp/83.2.236
https://doi.org/10.1093/ajcp/83.2.236
Publikováno v:
Cancer Genetics and Cytogenetics. 16:13-19
Von Hippel-Lindau disease is inherited by an autosomal dominant gene that may show marked expressive variability of cancer phenotype in certain patients/families. We describe a patient with a strongly positive family history of this disease who, at a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bb4ff70bc79940ca8262bdf45db06de
https://doi.org/10.1016/0165-4608(85)90073-1
https://doi.org/10.1016/0165-4608(85)90073-1
Publikováno v:
Chest. 95(2)
Primary neurogenic tumors of the lung are rare. Often, their histologic behavior presents a treatment dilemma. We present a case of benign endobronchial neurilemmoma managed by means of YAG laser resection together with a brief discussion of the mana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73a33caf4c663d4bfc097808a7ed04b
https://pubmed.ncbi.nlm.nih.gov/2914500
https://pubmed.ncbi.nlm.nih.gov/2914500
Publikováno v:
Archives of dermatology. 120(11)
Subcutaneous fat necrosis of the newborn (SFNN) usually occurs during the first few weeks of life. 1 It is characterized by necrosis of the subcutaneous fat with needle-shaped crystal formations within the fat cells. This process initiates a localize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::304a87e56a48f50f1917674f77de1a16
https://pubmed.ncbi.nlm.nih.gov/6497421
https://pubmed.ncbi.nlm.nih.gov/6497421
Autor:
Patrick Bogard, Cindy A. Wagner, Henry T. Lynch, Jane F. Lynch, Gerard J. Voorhees, David Katz
Publikováno v:
The American journal of medicine. 78(5)
Familial testicular cancer is rare. This report describes a family with an unusual cancer spectrum that included the infantile form of embryonal carcinoma of the testis in the son of a cancer-free but putative obligate gene carrier mother, and the ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::756728570d2f45cfd59b2536c69cc496
https://pubmed.ncbi.nlm.nih.gov/3993670
https://pubmed.ncbi.nlm.nih.gov/3993670
Publikováno v:
American journal of diseases of children (1960). 139(2)
• We studied two children who had rhabdomyosarcoma and glioblastoma and who were from a family with a hereditary cancer syndrome that was characterized by sarcoma, breast cancer, brain tumors, lung cancer, laryngeal carcinoma, leukemia, and adrenoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00103376f9cc91bb2ccd35efc2073b81
https://pubmed.ncbi.nlm.nih.gov/3976585
https://pubmed.ncbi.nlm.nih.gov/3976585
Publikováno v:
American journal of obstetrics and gynecology. 148(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0c138aee14bc68563edb7e7297b2e6
https://pubmed.ncbi.nlm.nih.gov/6695982
https://pubmed.ncbi.nlm.nih.gov/6695982