Ví dụ về việc sử dụng Cck trong Tiếng anh và bản dịch của chúng sang Tiếng việt
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I have following cck.
But CCK doesn't just stay in your gut.
This draft is based on CCK, OFDM, and PBCC technologies.
CCK and gastrin share the same five C-terminal amino acids.
The effects of CCK vary between individuals.
CCK also causes the release of digestive enzymes from the pancreas.
CBO fast acting, and CCK and CCL dual-element time-delay fuses.
Second, high-fat foods stimulate the release of the hormone cholecystokinin(CCK).
The release of CCK is also inhibited by somatostatin and pancreatic peptide.
It also regulates sleep, so if you feel satisfied and sleepy after a meal,you have CCK to thank.
Mg CCK boosting complex, with cha-de-bugre, apple pectin and more.
I have created a rule that when post is created in our ticket system,we have a node reference CCK field were the user can be selected; an email is sent to that user notifiying.
The existence of CCK was first suggested in 1905 by the British physiologist Joy Simcha Cohen[3][4].
This project provides D7 versions of the'node_reference' and'user_reference' field types,that were part of the CCK package in D6, at functional parity with the D6 counterparts. See….
CCK in the body cannot cross the blood-brain barrier, but certain parts of the hypothalamus and brainstem are not protected by the barrier.
For instance, the basic information about the nodes of your site are stored in the Node table,and if you use the CCK module to add fields to your nodes, the field information is stored in separate tables.
Thus, the CCK peptide hormone exists in several forms, each identified by the number of amino acids it contains, e.g., CCK58, CCK33, CCK22 and CCK8.
For example, the basic information regarding the nodes of your site are stored and kept in the node table,and if you use the CCK module to add fields to your nodes, the field information is stored in a separate table.
As a peptide hormone, CCK mediates satiety by acting on the CCK receptors distributed widely throughout the central nervous system.
Unlike the previous version which was heavily dependent on the module by Drupal community(Contributed modules),Drupal 7 has integrated these modules(eg, CCK, Cron. vv) into core part to become a strong CMS.
Levels of hormones that make us feel full- CCK, PYY, GLP-1, amylin and insulin- all increase following a meal to reach a peak about 30 to 60 minutes later.
CCK plays important physiological roles both as a neuropeptide in the central nervous system and as a peptide hormone in the gut.[8] It participates in a number of processes such as digestion, satiety and anxiety.
The mechanism for hunger suppression is thought to be a decrease in the rate of gastric emptying.[12] CCK also has stimulatory effects on the vagus nerve, effects that can be inhibited by capsaicin.[13] The stimulatory effects of CCK oppose those of ghrelin, which has been shown to inhibit the vagus nerve.
CCK is synthesized and released by enteroendocrine cells in the mucosal lining of the small intestine(mostly in the duodenum and jejunum), called I cells, neurons of the enteric nervous system, and neurons in the brain.
For example, in rats, CCK administration significantly reduces hunger in adult males, but is slightly less effective in younger subjects, and even slightly less effective in females.
CCKB receptor also binds gastrin, a gastrointestinal hormone involved in stimulating gastric acid release andgrowth of the gastric mucosa.[19][20][21] CCK has also been shown to interact with calcineurin in the pancreas.
CCK can be stimulated by a diet high in protein, or by protease inhibitors.[22] CCK has been shown to interact with orexin neurons, which control appetite and wakefulness(sleep).[23] CCK can have indirect effects on sleep regulation.
CCK is synthesized and released by enteroendocrine cells in the mucosal lining of the small intestine(mostly in the duodenum and jejunum), called I cells, neurons of the enteric nervous system, and neurons in the brain.[1] It is released rapidly into the circulation in response to a meal.
CCK is composed of varying numbers of amino acids depending on post-translational modification of the 150-amino acid precursor, preprocholecystokinin.[5] Thus, the CCK peptide hormone exists in several forms, each identified by the number of amino acids it contains, e.g., CCK58, CCK33, CCK22 and CCK8.
Most CCK peptides have a sulfate group attached to a tyrosine located seven residues from the C-terminus(see tyrosine sulfation).[5] This modification is crucial for the ability of CCK to activate the cholecystokinin A receptor. Nonsulfated CCK peptides also occur, which consequently cannot activate the CCK-A receptor, but their biological role remains unclear.