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substance p and Cystic Fibrosis of Pancreas

substance p has been researched along with Cystic Fibrosis of Pancreas in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Choi, JY; Joo, NS; Khansaheb, M; Krouse, ME; Robbins, RC; Weill, D; Wine, JJ1
Cho, HJ; Joo, NS; Khansaheb, M; Wine, JJ1
Cho, HJ; Joo, NS; Wine, JJ1
Dreshaj, IA; Ferkol, T; Haxhiu, MA; Kelley, TJ; Martin, RJ; Mhanna, MJ; van Heeckeren, AM1
Cannon, D; Cusack, D; Powell, D; Skrabanek, P1
Brengelmann, GL; Buchan, AM; Freund, PR; Savage, MV1

Other Studies

6 other study(ies) available for substance p and Cystic Fibrosis of Pancreas

ArticleYear
Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.
    The Journal of clinical investigation, 2009, Volume: 119, Issue:5

    Topics: Age Factors; Animals; Calcium Signaling; Capsicum; Carbachol; Chelating Agents; Clotrimazole; Colforsin; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dose-Response Relationship, Drug; Drug Synergism; Egtazic Acid; Exocrine Glands; Female; Humans; In Vitro Techniques; Male; Mucus; Plant Oils; Substance P; Sus scrofa; Trachea; Vasoactive Intestinal Peptide

2009
Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.
    The Journal of clinical investigation, 2010, Volume: 120, Issue:9

    Topics: Animals; Animals, Newborn; Body Fluids; Carbachol; Colforsin; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Epithelial Cells; Exocrine Glands; Respiratory System; Substance P; Sus scrofa; Trachea

2010
Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs.
    PloS one, 2011, Volume: 6, Issue:8

    Topics: Aging; Animals; Animals, Newborn; Body Fluids; Carbachol; Colforsin; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Drug Synergism; Exocrine Glands; Mutation; Organ Size; Substance P; Sus scrofa; Trachea; Turbinates

2011
Nitric oxide deficiency contributes to impairment of airway relaxation in cystic fibrosis mice.
    American journal of respiratory cell and molecular biology, 2001, Volume: 24, Issue:5

    Topics: Animals; Arginine; Bronchoconstriction; Cystic Fibrosis; Dinoprostone; Disease Models, Animal; Electric Stimulation; Enzyme Inhibitors; Female; In Vitro Techniques; Male; Mice; Mice, Inbred CFTR; Muscle Relaxation; Nitric Oxide; Nitric Oxide Synthase; Nitroarginine; Substance P; Trachea

2001
Substance P plasma levels in pregnancy and in various clinical disorders.
    Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 1979, Volume: 11, Issue:7

    Topics: Cystic Fibrosis; Female; Humans; Intestinal Diseases; Neoplasms; Pregnancy; Radioimmunoassay; Substance P; Thyroid Diseases

1979
Cystic fibrosis, vasoactive intestinal polypeptide, and active cutaneous vasodilation.
    Journal of applied physiology (Bethesda, Md. : 1985), 1990, Volume: 69, Issue:6

    Topics: Adult; Biopsy; Blood Pressure; Body Temperature Regulation; Calcitonin Gene-Related Peptide; Cystic Fibrosis; Forearm; Hot Temperature; Humans; Male; Neuropeptide Y; Reference Values; Regional Blood Flow; Skin; Skin Temperature; Substance P; Sweating; Vasoactive Intestinal Peptide; Vasodilation

1990