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Mark   Year Entries
Cyrus, the Great, King of Persia, -530 B.C. or 529 B.C. -- Juvenile literature. : Cyrus the Great ; and, Alexander the Great  1926 1
Cyrus, the Younger, approximately 423 B.C.-401 B.C.   9
 

Cyrus, the Younger's Expedition, 401 B.C -- See Greece History Expedition of Cyrus, 401 B.C


  1
Cysner, Joseph, 1912-1961. : Philippine sanctuary : a Holocaust odyssey / Bonnie M. Harris  2020 1
Cyst Fluid -- cytology. : Cytopathology of the head and neck : ultrasound guided FNAC / author: Gabrijela Kocjan ; contributor: Simon Morley  2017 1
 

Cyst, Hydatid -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation
  1
 

Cyst, Mediastinal -- See Mediastinal Cyst


Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus
  1
Cyst nematodes.   2
Cyst nematodes -- Classification. : Systematics of cyst nematodes (nematoda: heteroderinae). 8B / Sergei A. Subbotin, Manuel Mundo-Ocampo and James G. Baldwin  2010 1
Cyst nematodes -- Cytology : Cell biology of plant nematode parasitism / R. Howard Berg, Christopher G. Taylor, editors  2009 1
 

Cyst, Neurenteric -- See Neural Tube Defects


Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41)
  1
 

Cyst, Neuroenteric -- See Neural Tube Defects


Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41)
  1
 

Cyst, Pericardial -- See Mediastinal Cyst


Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus
  1
 

Cyst, Thoracic -- See Mediastinal Cyst


Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus
  1
 

Cyst, Thymic -- See Mediastinal Cyst


Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus
  1
 

Cyst, Tracheal -- See Mediastinal Cyst


Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus
  1
 

Cystadane -- See Betaine


  1
 

Cystatin-Related Proteins -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
  Cystatin superfamily -- 2 Related Subjects   2
Cystatins. : Cystatins : protease inhibitors, biomarkers, and immunomodulators / John B. Cohen and Linda P. Ryseck, editors  2011 1
 

Cystatins, Type 1 -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystatins, Type 2 -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystatins, Type 3 -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystatins, Type I -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystatins, Type II -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystatins, Type III -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Cystectomies -- See Cystectomy


Used for excision of the urinary bladder
  1
 

Cystectomy -- See Also Urinary Diversion


Temporary or permanent diversion of the flow of urine through the ureter away from the URINARY BLADDER in the presence of a bladder disease or after cystectomy. There is a variety of techniques: direct anastomosis of ureter and bowel, cutaneous ureterostomy, ileal, jejunal or colon conduit, ureterosigmoidostomy, etc. (From Campbell's Urology, 6th ed, p2654)
  1
Cystectomy : Keys to successful orthotopic bladder substitution / Urs E. Studer, editor  2015 1
Cystectomy -- methods : Endourological management of urogenital carcinoma / S. Naito, Y. Hirao, T. Terachi (eds.)  2006 1
Cysteine Endopeptidases   2
Cysteine Proteases -- chemistry : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine Proteases -- immunology : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine Proteinase Inhibitors : Design of caspase inhibitors as potential clinical agents / edited by Tom O'Brien, Steven D. Linton  2009 1
 

Cysteine proteinases -- See Also the narrower term Calpain


  1
Cysteine proteinases.   2
 

Cysteine proteinases Inhibitors -- See Also the narrower term Cystatins


  1
Cysteine proteinases -- Inhibitors.   3
Cysteine proteinases -- Pathophysiology : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine -- Therapeutic use : The therapeutic use of N-Acetylcysteine (NAC) in medicine / Richard Eugene Frye, Michael Berk, editors  2019 1
 

Cystic disease of the kidney -- See Kidney, Cystic


  1
 

Cystic Echinocccoses -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation
  1
 

Cystic Echinocccosis -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation
  1
 

Cystic Fibrosis -- See Also Cystic Fibrosis Transmembrane Conductance Regulator


A chloride channel that regulates secretion in many exocrine tissues. Abnormalities in the CFTR gene have been shown to cause cystic fibrosis. (Hum Genet 1994;93(4):364-8)
  1
Cystic fibrosis.   39
Cystic Fibrosis Association of Victoria. / http://id.loc.gov/authorities/names/n00138148 : Cystic fibrosis handbook / Teresa Bennington ... [and others]  1998 1
Cystic fibrosis -- Australia -- Victoria. : Cystic fibrosis care : quality of care guidelines / recommendations of the Victorian Clinical Standards Advisory Group on Cystic Fibrosis  1999 1
Cystic Fibrosis -- complications   2
Cystic fibrosis -- Congresses. : Current problems and new trends in cystic fibrosis : 10th meeting of the European Working Group for Cystic Fibrosis, Bern, September 22-23, 1981 / volume editors: M. Schoni and R. Kraemer  1981 1
Cystic fibrosis -- Diagnosis. : Cystic fibrosis in primary care : an essential guide to a complex, multi-system disease / Douglas Lewis, editor  2020 1
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