Zobrazeno 1 - 10
of 35
pro vyhledávání: '"A Delgado-Verdugo"'
Autor:
Tobias Åkerström, Joakim Crona, Alberto Delgado Verdugo, Lee F Starker, Kenko Cupisti, Holger S Willenberg, Wolfram T Knoefel, Wolfgang Saeger, Alfred Feller, Julian Ip, Patsy Soon, Martin Anlauf, Pier F Alesina, Kurt W Schmid, Myriam Decaussin, Pierre Levillain, Bo Wängberg, Jean-Louis Peix, Bruce Robinson, Jan Zedenius, Martin Bäckdahl, Stefano Caramuta, K Alexander Iwen, Johan Botling, Peter Stålberg, Jean-Louis Kraimps, Henning Dralle, Per Hellman, Stan Sidhu, Gunnar Westin, Hendrik Lehnert, Martin K Walz, Göran Åkerström, Tobias Carling, Murim Choi, Richard P Lifton, Peyman Björklund
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41926 (2012)
Aldosterone producing lesions are a common cause of hypertension, but genetic alterations for tumorigenesis have been unclear. Recently, either of two recurrent somatic missense mutations (G151R or L168R) was found in the potassium channel KCNJ5 gene
Externí odkaz:
https://doaj.org/article/8e3599de100c4ef9802dce0a7af360fa
Autor:
Peyman Björklund, Per Hellman, A. Delgado Verdugo, Gunnar Westin, Rajani Maharjan, Joakim Crona
Publikováno v:
Hormone and Metabolic Research. 47:452-455
The genetic background in small intestinal neuroendocrine tumors is poorly understood, but several studies have revealed numerical imbalances. Loss of one copy of chromosome 18 is the most frequent genetic aberration in this tumor type, which indirec
Autor:
Monica Sandberg, Örjan Källskog, A. Erik G. Persson, Alberto Delgado Verdugo, Ulrika Pettersson, Leif Jansson, Per-Ola Carlsson, Birgitta Bodin, En Yin Lai
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 307:E653-E663
Pancreatic islet blood perfusion varies according to the needs for insulin secretion. We examined the effects of blood lipids on pancreatic islet blood flow in anesthetized rats. Acute administration of Intralipid to anesthetized rats increased both
Autor:
Alberto Delgado Verdugo, Joakim Crona, Dan Granberg, Per Hellman, Peter Stålberg, Peyman Björklund, Rajani Maharjan
Publikováno v:
Familial Cancer. 13:121-125
Pheochromocytoma (PCC) and Paraganglioma are rare tumours originating from neuroendocrine cells. Up to 60 % of cases have either germline or somatic mutation in one of eleven described susceptibility loci, SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, EPAS1,
Autor:
Robert Udelsman, William D. Long, Alberto Delgado-Verdugo, Lee F. Starker, Patricia Donovan, Richard P. Lifton, Tobias Carling, Tobias Åkerström
Publikováno v:
Hormones and Cancer. 3:44-51
Familial primary hyperparathyroidism (FPHPT) may occur due to an underlying germ-line mutation in the MEN1, CASR, or HRPT2/CDC73 genes. The disease may be undiagnosed in the absence of a history suggestive of FHPT. Young PHPT patients (≤45 years of
Publikováno v:
Endocrine. 38:397-401
To investigate the SDHAF2 gene and its effect on primary hyperparathyroidism. Parathyroid tumors causing primary hyperparathyroidism (pHPT) are one of the more common endocrine neoplasias. Loss of heterozygosity at chromosome 11q13 is the most common
Autor:
Enyin, Lai, Ulrika, Pettersson, Alberto Delgado, Verdugo, Per-Ola, Carlsson, Birgitta, Bodin, Örjan, Källskog, A Erik G, Persson, Monica, Sandberg, Leif, Jansson
Publikováno v:
American journal of physiology. Endocrinology and metabolism. 307(8)
Pancreatic islet blood perfusion varies according to the needs for insulin secretion. We examined the effects of blood lipids on pancreatic islet blood flow in anesthetized rats. Acute administration of Intralipid to anesthetized rats increased both
Autor:
Delgado Verdugo, Alberto
Endocrine tumors arise from endocrine glands. Most endocrine tumors are benign but malignant variants exist. Several endocrine neoplasms display loss of parts of chromosome 11 or 18, produce hormones and responds poorly to conventional chemotherapeut
Externí odkaz:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-224111
Autor:
Göran Åkerström, Joakim Crona, Gunnar Westin, Alberto Delgado Verdugo, Peyman Björklund, Peter Stålberg, Lee F. Starker, Per Hellman
Publikováno v:
Endocrine-related cancer. 21(1)
Endocrine tumors arise from endocrine glands. Most endocrine tumors are benign but malignant variants exist. Several endocrine neoplasms display loss of parts of chromosome 11 or 18, produce hormones and responds poorly to conventional chemotherapeut
Autor:
Dan Granberg, Rajani Maharjan, Joakim Crona, Peyman Björklund, Per Hellman, Alberto Delgado Verdugo, Peter Stålberg
Publikováno v:
The Journal of clinical endocrinology and metabolism. 98(7)
Context: Up to 60% of pheochromocytoma (PCC) and paraganglioma (PGL) are associated with either somatic or germline mutations in established PCC and PGL susceptibility loci. Most unexplained cases are characterized by an increased activity of the RAS