Targeting of cholecystokinin receptor expressing malignancies such as medullary thyroid carcinoma is currently limited by low in vivo stability of radioligands. To increase the stability, we have developed and preclinically evaluated two cyclic 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-minigastrin analogs radiolabeled with (111)In and (68)Ga
Cholecystokinin subtype 2 receptors (CCK2R) are overexpressed in several human cancers, including me...
The high overexpression of cholecystokinin-2 receptors (CCK2R) in tumors, such as medullary thyroid ...
The cholecystokinin-2 receptor (CCK2R) is an attractive target in nuclear medicine due to its overex...
PURPOSE: Targeting of cholecystokinin receptor expressing malignancies such as medullary thyroid car...
Different attempts have been made in the past two decades to develop radiolabeled peptide conjugates...
Item does not contain fulltextCholecystokinin-2 (CCK-2) receptors, overexpressed in cancer types suc...
The new minigastrin analog DOTA-MGS5 is a promising new candidate for targeting cholecystokinin-2 re...
Introduction A variety of radiolabelled minigastrin analogues targeting the cholecystokinin 2 (CCK2)...
The development of suitable radioligands for targeting CCK-2 receptor expressing tumours, such as me...
Two cyclized minigastrin analogues for gastrin receptor scintigraphy were synthesized and derivatize...
The development of metabolically stable radiolabeled gastrin analogues with suitable pharmacokinetic...
In comparison to somatostatin receptor scintigraphy, gastrin receptor scintigraphy using 111In-DTPA-...
In comparison to somatostatin receptor scintigraphy, gastrin receptor scintigraphy using 111In-DTPA-...
PURPOSE: Diethylenetriamine-pentaacetic acid (DTPA)-coupled minigastrins are unsuitable for therapeu...
Medullary thyroid carcinoma (MTC) expresses CCK-2 receptors. (111)In-labeled DOTA-DGlu-Ala-Tyr-Gly-T...
Cholecystokinin subtype 2 receptors (CCK2R) are overexpressed in several human cancers, including me...
The high overexpression of cholecystokinin-2 receptors (CCK2R) in tumors, such as medullary thyroid ...
The cholecystokinin-2 receptor (CCK2R) is an attractive target in nuclear medicine due to its overex...
PURPOSE: Targeting of cholecystokinin receptor expressing malignancies such as medullary thyroid car...
Different attempts have been made in the past two decades to develop radiolabeled peptide conjugates...
Item does not contain fulltextCholecystokinin-2 (CCK-2) receptors, overexpressed in cancer types suc...
The new minigastrin analog DOTA-MGS5 is a promising new candidate for targeting cholecystokinin-2 re...
Introduction A variety of radiolabelled minigastrin analogues targeting the cholecystokinin 2 (CCK2)...
The development of suitable radioligands for targeting CCK-2 receptor expressing tumours, such as me...
Two cyclized minigastrin analogues for gastrin receptor scintigraphy were synthesized and derivatize...
The development of metabolically stable radiolabeled gastrin analogues with suitable pharmacokinetic...
In comparison to somatostatin receptor scintigraphy, gastrin receptor scintigraphy using 111In-DTPA-...
In comparison to somatostatin receptor scintigraphy, gastrin receptor scintigraphy using 111In-DTPA-...
PURPOSE: Diethylenetriamine-pentaacetic acid (DTPA)-coupled minigastrins are unsuitable for therapeu...
Medullary thyroid carcinoma (MTC) expresses CCK-2 receptors. (111)In-labeled DOTA-DGlu-Ala-Tyr-Gly-T...
Cholecystokinin subtype 2 receptors (CCK2R) are overexpressed in several human cancers, including me...
The high overexpression of cholecystokinin-2 receptors (CCK2R) in tumors, such as medullary thyroid ...
The cholecystokinin-2 receptor (CCK2R) is an attractive target in nuclear medicine due to its overex...