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The chronically reserpinized rat as a model for cystis fibrosis: abnormal Cl- transport as the basis for reduced salivary fluid secretion

Author
RICARDO MARTINEZ, J1 ; CASSITY, N
[1] Univ. Missouri, school medicine, Columbia MO 65212, United States
Source

Pediatric research. 1985, Vol 19, Num 7, pp 711-716 ; ref : 22 ref

CODEN
PEREBL
ISSN
0031-3998
Scientific domain
Genetics; Pediatrics
Publisher
Lippincott Williams & Wilkins, Hagerstown, MD
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Appareil digestif pathologie Appareil respiratoire pathologie Chlore Elément minéral Enfant Etiopathogénie Glande sousmaxillaire Modèle animal Mucoviscidose Pancréas pathologie Rat Réserpine Salive Sécrétion Trouble métabolisme Homme Mammalia Rodentia Vertebrata
Keyword (en)
Digestive diseases Respiratory disease Chlorine Inorganic element Child Etiopathogenesis Submandibular gland Animal model Mucoviscidosis Pancreatic disease Rat Saliva Secretion Metabolic disorder Human Mammalia Rodentia Vertebrata
Keyword (es)
Aparato digestivo patologia Aparato respiratorio patologia Cloro Elemento mineral Niño Etiopatogenia Modelo animal Mucoviscidosis Pancreas patologia Rata Saliva Secrecion
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B13 Gastroenterology. Liver. Pancreas. Abdomen / 002B13C Liver. Biliary tract. Portal circulation. Exocrine pancreas / 002B13C03 Other diseases. Semiology

Discipline
Gastroenterology. Liver. Pancreas. Abdomen
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
9210826

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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