Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: PDPK1[original query] |
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Mutational and immunohistochemical study of the PI3K/Akt pathway in papillary thyroid carcinoma in Greece. Endocrine pathology 2010 Jun 21 (2): 90-100. Sozopoulos Elias, Litsiou Helen, Voutsinas Gerassimos, Mitsiades Nikolaos, Anagnostakis Nikolaos, Tseva Thomais, Patsouris Efstratios, Tseleni-Balafouta Sof |
Roles of genetic variants in the PI3K and RAS/RAF pathways in susceptibility to endometrial cancer and clinical outcomes. Journal of cancer research and clinical oncology 2012 Mar 138 (3): 377-85. Wang Li-E, Ma Hongxia, Hale Katherine S, Yin Ming, Meyer Larissa A, Liu Hongliang, Li Jie, Lu Karen H, Hennessy Bryan T, Li Xuesong, Spitz Margaret R, Wei Qingyi, Mills Gordon |
Loss of PTEN expression is associated with poor prognosis in patients with intraductal papillary mucinous neoplasms of the pancreas. Clinical cancer research : an official journal of the American Association for Cancer Research 2013 Dec 19 (24): 6830-41. Garcia-Carracedo Dario, Turk Andrew T, Fine Stuart A, Akhavan Nathan, Tweel Benjamin C, Parsons Ramon, Chabot John A, Allendorf John D, Genkinger Jeanine M, Remotti Helen E, Su Gloria |
Alterations of INPP4B, PIK3CA and pAkt of the PI3K pathway are associated with squamous cell carcinoma of the lung. Cancer medicine 2014 Apr 3 (2): 337-48. Stjernström Annika, Karlsson Christina, Fernandez Oswaldo J, Söderkvist Peter, Karlsson Mats G, Thunell Lena |
Copy number variation of genes involved in the hepatitis C virus-human interactome. Scientific reports 2016 6 31340. Budzko Lucyna, Marcinkowska-Swojak Malgorzata, Jackowiak Paulina, Kozlowski Piotr, Figlerowicz Mar |
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Sep . Mucha Bettina E, Banka Siddharth, Ajeawung Norbert Fonya, Molidperee Sirinart, Chen Gary G, Koenig Mary Kay, Adejumo Rhamat B, Till Marianne, Harbord Michael, Perrier Renee, Lemyre Emmanuelle, Boucher Renee-Myriam, Skotko Brian G, Waxler Jessica L, Thomas Mary Ann, Hodge Jennelle C, Gecz Jozef, Nicholl Jillian, McGregor Lesley, Linden Tobias, Sisodiya Sanjay M, Sanlaville Damien, Cheung Sau W, Ernst Carl, Campeau Philippe |
Clinical and Genetic Investigation of Premature Ovarian Insufficiency Cases from Turkey. Journal of gynecology obstetrics and human reproduction 2019 Apr . Oral Engin, Toksoy Guven, Sofiyeva Nigar, Celik Hale Goksever, Karaman Birsen, Basaran Seher, Azami Asli, Uyguner Zehra O |
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