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Peptidylprolyl isomerase D (cyclophilin D), also known as PPID, is an enzyme which in humans is encoded by the PPID gene on chromosome 4. As a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family, this protein catalyzes the cis-trans isomerization of proline imidic peptide bonds, which allows it to facilitate folding or repair of proteins. [5]
Pituitary pars intermedia dysfunction (PPID), or equine Cushing's disease, is an endocrine disease affecting the pituitary gland of horses. It is most commonly seen in older animals, [ 1 ] and is classically associated with the formation of a long, wavy coat ( hirsutism ) and chronic laminitis .
PPID may refer to: Peptidylprolyl isomerase D, an enzyme encoded within the PPID gene; Pituitary pars intermedia dysfunction in horses. Computer Science.
PPID: ID number of the process's parent process PRI: Priority of the process RSS: Resident set size: S or STAT: Process status code START or STIME: Time when the process started VSZ: Virtual memory usage TIME: The amount of CPU time used by the process TT or TTY: Terminal associated with the process UID or USER: Username of the process's owner ...
On the Windows family of operating systems, one can get the current process's ID using the GetCurrentProcessId() function of the Windows API, [11] and ID of other processes using GetProcessId(). [12]
Fundic gland polyposis is a medical syndrome where the fundus and the body of the stomach develop many fundic gland polyps.The condition has been described both in patients with familial adenomatous polyposis (FAP) and attenuated variants (AFAP), and in patients in whom it occurs sporadically.
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The POMC gene is located on chromosome 2p23.3. The POMC gene is expressed in both the anterior and intermediate lobes of the pituitary gland. This gene encodes a 285-amino acid polypeptide hormone precursor that undergoes extensive, tissue-specific, post-translational processing via cleavage by subtilisin-like enzymes known as prohormone convertases.