Søgeresultater - Lines, Kate E

Current and Emerging Therapies for Pancreatic Neuroendocrine Tumours in Patients with or without Multiple Endocrine Neoplasia Type 1 af Frost, Morten, Lines, Kate E, Thakker, Rajesh V

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Molecular genetic studies of pancreatic neuroendocrine tumors reveal new therapeutic approaches af Stevenson, Mark, Lines, Kate E., Thakker, Rajesh V.

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The bromodomain inhibitor JQ1+ reduces calcium-sensing receptor activity in pituitary cell lines af Lines, Kate E, Gluck, Anna K, Thongjuea, Supat, Bountra, Chas, Thakker, Rajesh V, Gorvin, Caroline M

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Multiple Endocrine Neoplasia Type 1: Latest Insights af Brandi, Maria Luisa, Agarwal, Sunita K, Perrier, Nancy D, Lines, Kate E, Valk, Gerlof D, Thakker, Rajesh V

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Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1–Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progressio... af Walls, Gerard V., Stevenson, Mark, Soukup, Benjamin S., Lines, Kate E., Grossman, Ashley B., Schmid, Herbert A., Thakker, Rajesh V.

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The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing af Stevenson, Mark, Pagnamenta, Alistair T, Mack, Heather G, Savige, Judith, Giacopuzzi, Edoardo, Lines, Kate E, Taylor, Jenny C, Thakker, Rajesh V

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OR07-06 The Roles of GNAQ and GNA11 in Calcium-Sensing Receptor (CaSR) Signalling af Gluck, Anna K, Stevenson, Mark, Falcone, Sara, Inoue, Asuka, Breitwieser, Gerda E, Gorvin, Caroline M, Lines, Kate E, Thakker, Rajesh V

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Whole genome sequence analysis identifies a PAX2 mutation to establish a correct diagnosis for a syndromic form of hyperuricemia af Stevenson, Mark, Pagnamenta, Alistair T., Reichart, Silvia, Philpott, Charlotte, Lines, Kate E., Gorvin, Caroline M., Lhotta, Karl, Taylor, Jenny C., Thakker, Rajesh V.

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Multiple Endocrine Neoplasia Type 1 (MEN1) Phenocopy Due to a Cell Cycle Division 73 (CDC73) Variant af Lines, Kate E, Nachtigall, Lisa B, Dichtel, Laura E, Cranston, Treena, Boon, Hannah, Zhang, Xun, Kooblall, Kreepa G, Stevenson, Mark, Thakker, Rajesh V

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TWO SYNCHRONOUS PITUITARY ADENOMAS CAUSING CUSHING DISEASE AND ACROMEGALY af Schorr, Melanie, Zhang, Xun, Zhao, Wenxiu, Abedi, Parisa, Lines, Kate E., Hedley-Whyte, E. Tessa, Swearingen, Brooke, Klibanski, Anne, Miller, Karen K., Thakker, Rajesh V., Nachtigall, Lisa B.

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Activating Mutations of the G-protein Subunit α (11) Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2 af Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, Glück, Anna K, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E, Hannan, Fadil M, Thakker, Rajesh V

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Clinical MEN-1 Among a Large Cohort of Patients With Acromegaly af Nachtigall, Lisa B, Guarda, Francisco J, Lines, Kate E, Ghajar, Alireza, Dichtel, Laura, Mumbach, Giselle, Zhao, Wenxiu, Zhang, Xun, Tritos, Nicholas A, Swearingen, Brooke, Miller, Karen K, Thakker, Rajesh V

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PTH infusion ameliorates seizures in autosomal dominant hypocalcemia type 1 af Sastre, Ana, Valentino, Kevin, Hannan, Fadil M., Lines, Kate E., Gluck, Anna K., Stevenson, Mark, Ryalls, Michael, Pullen, Debbie, Buck, Jackie, Sankar, Sailesh, Allgrove, Jeremy, Thakker, Rajesh V., Gevers, Evelien F.

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Genetic background influences tumour development in heterozygous Men1 knockout mice af Lines, Kate E, Javid, Mahsa, Reed, Anita A C, Walls, Gerard V, Stevenson, Mark, Simon, Michelle, Kooblall, Kreepa G, Piret, Sian E, Christie, Paul T, Newey, Paul J, Mallon, Ann-Marie, Thakker, Rajesh V

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Association of prolactin receptor (PRLR) variants with prolactinomas af Gorvin, Caroline M, Newey, Paul J, Rogers, Angela, Stokes, Victoria, Neville, Matt J, Lines, Kate E, Ntali, Georgia, Lees, Peter, Morrison, Patrick J, Singhellakis, Panagiotis N, Malandrinou, Fotini Ch, Karavitaki, Niki, Grossman, Ashley B, Karpe, Fredrik, Thakker, Rajesh V

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Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause af Zhou, Junhua, Azizan, Elena A. B., Cabrera, Claudia P., Fernandes-Rosa, Fabio L., Boulkroun, Sheerazed, Argentesi, Giulia, Cottrell, Emily, Amar, Laurence, Wu, Xilin, O’Toole, Sam, Goodchild, Emily, Marker, Alison, Senanayake, Russell, Garg, Sumedha, Åkerström, Tobias, Backman, Samuel, Jordan, Suzanne, Polubothu, Satyamaanasa, Berney, Daniel M., Gluck, Anna, Lines, Kate E., Thakker, Rajesh V., Tuthill, Antoinette, Joyce, Caroline, Kaski, Juan Pablo, Frankl, Fiona E. Karet, Metherell, Lou A., Teo, Ada E. D., Gurnell, Mark, Parvanta, Laila, Drake, William M., Wozniak, Eva, Klinzing, David, Kuan, Jyn Ling, Tiang, Zenia, Gomez Sanchez, Celso E., Hellman, Per, Foo, Roger S. Y., Mein, Charles A., Kinsler, Veronica A., Björklund, Peyman, Storr, Helen L., Zennaro, Maria-Christina, Brown, Morris J.

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