cystic vein - meaning and definition. What is cystic vein
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  3. cystic vein

What (who) is cystic vein - definition


Cystic vein         
When present the cystic vein drains the blood from the gall-bladder, and, accompanying the cystic duct, usually ends in the right branch of the portal vein. It is usually not present, and the blood drains via small veins in the gall-bladder bed directly to the parenchyma of the liver.
https://en.wikipedia.org/wiki/Cystic_vein
cystic fibrosis         
  • Health problems associated with cystic fibrosis
  • The CFTR protein is a channel protein that controls the flow of H<sub>2</sub>O and Cl<sup>−</sup> ions in and out of cells inside the lungs. When the CFTR protein is working correctly, ions freely flow in and out of the cells. However, when the CFTR protein is malfunctioning, these ions cannot flow out of the cell due to a blocked channel. This causes cystic fibrosis, characterized by the buildup of thick mucus in the lungs.
  • The location of the ''CFTR'' gene on chromosome 7
  • Respiratory infections in CF vary according to age.<br><br>Green = ''[[Pseudomonas aeruginosa]]''<br>Brown = ''[[Staphylococcus aureus]]''<br>Blue = ''[[Haemophilus influenzae]]''<br>Red = ''[[Burkholderia cepacia]]'' complex
  • [[Dorothy Hansine Andersen]] first described cystic fibrosis in 1938.
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  • Intracytoplasmic sperm injection can be used to provide fertility for men with cystic fibrosis.
AUTOSOMAL RECESSIVE DISEASE CHARACTERIZED BY THE BUILDUP OF MUCUS
Mucoviscidosis; Cistic fibrosis; Cystic Fiborsis; Cystic fibrosis allele; Cystic fibrose; Mucoviscidose; Viscoidosis; Mucuviscoidosis; Mucoviscoidosis; Mucoviscidopsis; Fibrocystic disease of the pancreas; Cystic Fibrosis; Cyctic fibrosis; Cystic Fibrosis (CF); History of Cystic fibrosis; Gene therapy for cystic fibrosis; Treatment of cystic fibrosis
Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult.
N-UNCOUNT
cystic fibrosis         
  • Health problems associated with cystic fibrosis
  • The CFTR protein is a channel protein that controls the flow of H<sub>2</sub>O and Cl<sup>−</sup> ions in and out of cells inside the lungs. When the CFTR protein is working correctly, ions freely flow in and out of the cells. However, when the CFTR protein is malfunctioning, these ions cannot flow out of the cell due to a blocked channel. This causes cystic fibrosis, characterized by the buildup of thick mucus in the lungs.
  • The location of the ''CFTR'' gene on chromosome 7
  • Respiratory infections in CF vary according to age.<br><br>Green = ''[[Pseudomonas aeruginosa]]''<br>Brown = ''[[Staphylococcus aureus]]''<br>Blue = ''[[Haemophilus influenzae]]''<br>Red = ''[[Burkholderia cepacia]]'' complex
  • [[Dorothy Hansine Andersen]] first described cystic fibrosis in 1938.
  • script]])
  • Intracytoplasmic sperm injection can be used to provide fertility for men with cystic fibrosis.
AUTOSOMAL RECESSIVE DISEASE CHARACTERIZED BY THE BUILDUP OF MUCUS
Mucoviscidosis; Cistic fibrosis; Cystic Fiborsis; Cystic fibrosis allele; Cystic fibrose; Mucoviscidose; Viscoidosis; Mucuviscoidosis; Mucoviscoidosis; Mucoviscidopsis; Fibrocystic disease of the pancreas; Cystic Fibrosis; Cyctic fibrosis; Cystic Fibrosis (CF); History of Cystic fibrosis; Gene therapy for cystic fibrosis; Treatment of cystic fibrosis
¦ noun a hereditary disorder which affects the exocrine glands and results in the production of abnormally thick mucus, leading to the blockage of the pancreatic ducts, intestines, and bronchi.
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