प्लाज्मिन हिंदी उपयोग और उदाहरण

वे प्लाज्मिनोजन-उत्प्रेरक का स्राव करती हैं, जो प्लाज्मिनोजन को सक्रिय करता है और उसे पपड़ी को घोलने के लिये प्लाज्मिन में बदलता है।

यूरोकिनेस, एक स्वच्छ प्रोटीज़ एंजाइम, जिसे यूरोकिनेस-टाइप प्लाज्मिनोजेन एक्टिवेटर या uPA के रूप में भी जाना जाता है।

""यूरोकिनेस, एक स्वच्छ प्रोटीज़ एंजाइम, जिसे यूरोकिनेस-टाइप प्लाज्मिनोजेन एक्टिवेटर या uPA के रूप में भी जाना जाता है।

प्लाज्मिन इसके अंग्रेजी अर्थ का उदाहरण

Tissue plasminogen activator (TPA) Activase by Genentech.

Urinary type plasminogen activator.

A single, modified TEG assay with exogenous tissue plasminogen activator (tPA) demonstrated remarkable efficiency in unmasking patients' impending risk for massive transfusion in trauma patients.

20th-century German mathematicians Aceruloplasminemia is a rare autosomal recessive disorder in which the liver can not synthesis the protein ceruloplasmin properly, which is needed to transport copper around the blood.

Aceruloplasminemia has been seen worldwide, but its overall prevalence is unknown.

Aceruloplasminemia belongs to the group of genetic disorders called neurodegeneration with brain iron accumulation (NBIA).

Patients with aceruloplasminemia develop a variety of movement problems.

Aceruloplasminemia is caused by a mutation (a five-base pair insertion in exon 7) in the CP gene, which provides instructions for making a protein called ceruloplasmin, a protein involved in iron transport and processing.

Ceruloplasmin helps move iron from the organs and tissues of the body and prepares it for incorporation into a molecule called transferrin, which transports it to red blood cells to help carry oxygen.

The CP gene mutation results in the production of ceruloplasmin protein that is unstable or nonfunctional by altering the open reading frame such that the amino acid ligands in the essential carboxyl terminal region are eliminated.

When ceruloplasmin is unavailable, transport of iron out of the body's tissues is impaired.

Diagnosis of this disorder depends on blood tests demonstrating the absence of serum ceruloplasmin, combined with low serum copper concentration, low serum iron concentration, high serum ferritin concentration, or increased [iron concentration.