Results 21 to 30 of about 39,719 (247)

Ca2+ binding to Chromaffin Vesicle Matrix Proteins [PDF]

open access: yes, 1986
Recently we found that Ca2+ within chromaffin vesicles is largely bound [Bulenda, D., & Gratzl, M. (1985) Biochemistry 24, 7760-77651. In order to explore the nature of these bonds, we analyzed the binding of Ca2+ to the vesicle matrix proteins as well ...
Gratzl, Manfred, Reiffen, F. U.
core   +1 more source

Neuroendocrine Carcinoma of the Stomach-A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Neuroendocrine carcinomas of stomach have been considered a rare neoplasm. The present case concerns with a 69 year old male, who presented with vague abdominal discomfort and history of malena.
Poorana Priya P.   +2 more
doaj   +1 more source

Unusual Presentation of Primary Ovarian Carcinoid Tumours with Low-toModerate Proliferative Potential [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
Primary Ovarian Carcinoid Tumour (OCT) are rare benign neuroendocrine neoplasms. Herewith, two cases of ovarian tumour has been described. In case 1, patient was a 63-year-old postmenopausal woman with vague abdominal pain.
Supriya Mehrotra   +4 more
doaj   +1 more source

Chromogranin A and chromogranin B in pancreatic neuroendocrine tumors

open access: yesMedical alphabet, 2020
For the first time in Russia a comparative study of chromogranin A (CgA) and chromogranin B (CgB) in neuroendocrine tumors (NETs) of the pancreas was performed. We examined 50 primary patients with pancreatic NETs and 42 healthy people. The determination of CgA and CgB was performed in blood serum using standard enzyme-linked immunoassay test-systems ...
N. V. Lyubimova   +3 more
openaire   +2 more sources

FGFR2 amplification in colorectal adenocarcinoma [PDF]

open access: yes, 2017
FGFR2 is recurrently amplified in 5% of gastric cancers and 1%–4% of breast cancers; however, this molecular alteration has never been reported in a primary colorectal cancer specimen.
Carter, Jamal H   +6 more
core   +2 more sources

Hepatic progenitor cells from adult human livers for cell transplantation. [PDF]

open access: yes, 2008
Objective: Liver regeneration is mainly based on cellular self-renewal including progenitor cells. Efforts have been made to harness this potential for cell transplantation, but shortage of hepatocytes and premature differentiated progenitor cells ...
Aurich, H.   +10 more
core   +1 more source

Neoadjuvant chemotherapy with capecitabine and temozolomide for unresectable pancreatic neuroendocrine tumor. [PDF]

open access: yes, 2012
Pancreatic neuroendocrine tumors (PNETs) are relatively rare tumors that arise in the endocrine cells of the pancreas. Historically, somatostatin analogues have been used in this disease primarily for symptom control and, to a limited extent, disease ...
Devata, Sumana, Kim, Edward J
core   +2 more sources

An unusual case of proton pump inhibitor induced hyperchromograninemia

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2019
Objective: To describe an unusual case of symptomatic hyperchromograninemia associated with proton pump inhibitor (PPI) use. Case Summary: A 55-year-old man with stage 1 follicular lymphoma and GERD on omeprazole presented with symptoms suggesting ...
Kwabena Oware Adu-Gyamfi   +2 more
doaj   +1 more source

bak deletion stimulates gastric epithelial proliferation and enhances Helicobacter felis-induced gastric atrophy and dysplasia in mice [PDF]

open access: yes, 2015
Helicobacter infection causes a chronic superficial gastritis that in some cases progresses via atrophic gastritis to adenocarcinoma. Proapoptotic bak has been shown to regulate radiation-induced apoptosis in the stomach and colon and also susceptibility
Abuderman, A A   +5 more
core   +2 more sources

Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family [PDF]

open access: yes, 2020
Head and neck paragangliomas are the most common clinical features of familial paraganglioma syndrome type 1 caused by succinate dehydrogenase complex subunit D (SDHD) mutation. The clinical management of this syndrome is still unclear.
Cantisani, Vito   +12 more
core   +1 more source

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