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Academic Journal

LAT1-dependent placental methionine uptake is a key player in fetal programming of metabolic disease.

  • Authors : Schroeder M; Faculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Switzerland; Swiss National Centre of Competence in Research, NCCR TransCure, University of Bern, Bern, Switzerland. Electronic address: .

Subjects: Fetal Development* ; Metabolic Diseases*/Metabolic Diseases*/Metabolic Diseases*/genetics ; Methionine*/Methionine*/Methionine*/metabolism

  • Source: Metabolism: clinical and experimental [Metabolism] 2024 Apr; Vol. 153, pp. 155793. Date of Electronic Publication: 2024 Jan 29.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0375267 Publication Model: Print-Electronic Cited

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Academic Journal

Antifibrotic Agents for the Management of CKD: A Review.

  • Authors : Ruiz-Ortega M; Molecular and Cellular Biology in Renal and Vascular Pathology, Madrid, Spain; Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid

Subjects: Idiopathic Pulmonary Fibrosis*/Idiopathic Pulmonary Fibrosis*/Idiopathic Pulmonary Fibrosis*/complications ; Renal Insufficiency, Chronic*/Renal Insufficiency, Chronic*/Renal Insufficiency, Chronic*/etiology; Adaptor Proteins, Signal Transducing

  • Source: American journal of kidney diseases : the official journal of the National Kidney Foundation [Am J Kidney Dis] 2022 Aug; Vol. 80 (2), pp. 251-263. Date of Electronic Publication: Publisher: W.B. Saunders Country of Publication: United States NLM ID: 8110075 Publication Model: Print-Electronic Cited

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Academic Journal

Autoantibodies to dense-fine-speckled 70 (DFS70) do not necessarily rule out connective tissue diseases.

  • Authors : Mockenhaupt LM; Clinic of Internal Medicine III, Department of Oncology, Hematology, Rheumatology and Clinical Immunology, University Hospital Bonn, Venusberg Campus 1, Bonn 53127, Germany. Electronic address: .; Dolscheid-Pommerich R

Subjects: Autoimmune Diseases* ; Connective Tissue Diseases*/Connective Tissue Diseases*/Connective Tissue Diseases*/diagnosis; Adaptor Proteins, Signal Transducing

  • Source: Seminars in arthritis and rheumatism [Semin Arthritis Rheum] 2022 Feb; Vol. 52, pp. 151936. Date of Electronic Publication: 2021 Dec 30.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 1306053 Publication Model: Print-Electronic Cited

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Academic Journal

Genetics of Sost/SOST in sclerosteosis and van Buchem disease animal models.

  • Authors : Sebastian A; Biology and Biotechnology Division, Lawrence Livermore National Laboratory, 7000 East Avenue, L-452, Livermore, CA 94550, USA.; Loots GG

Subjects: Bone Morphogenetic Proteins/Bone Morphogenetic Proteins/Bone Morphogenetic Proteins/*genetics ; Genetic Markers/Genetic Markers/Genetic Markers/*genetics ; Hyperostosis/Hyperostosis/Hyperostosis/*genetics Sclerosteosis

  • Source: Metabolism: clinical and experimental [Metabolism] 2018 Mar; Vol. 80, pp. 38-47. Date of Electronic Publication: 2017 Oct 25.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0375267 Publication Model: Print-Electronic Cited

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Academic Journal

Low periostin levels in adult patients with Langerhans cell histiocytosis are independently associated with the disease activity.

Subjects: Cell Adhesion Molecules/Cell Adhesion Molecules/Cell Adhesion Molecules/*blood ; Cell Adhesion Molecules/Cell Adhesion Molecules/Cell Adhesion Molecules/*deficiency ; Histiocytosis, Langerhans-Cell/Histiocytosis, Langerhans-Cell/Histiocytosis, Langerhans-Cell/*blood

  • Source: Metabolism: clinical and experimental [Metabolism] 2017 Jun; Vol. 71, pp. 198-201. Date of Electronic Publication: 2017 Apr 04.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0375267 Publication Model: Print-Electronic Cited

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Academic Journal

Relevance of serum sclerostin concentrations in critically ill patients.

  • Authors : Koch A; Department of Medicine III, RWTH-University Hospital Aachen, Aachen, Germany.; Weiskirchen R

Subjects: Intensive Care Units*; Bone Morphogenetic Proteins/Bone Morphogenetic Proteins/Bone Morphogenetic Proteins/*blood ; Sepsis/Sepsis/Sepsis/*blood

  • Source: Journal of critical care [J Crit Care] 2017 Feb; Vol. 37, pp. 38-44. Date of Electronic Publication: 2016 Aug 22.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 8610642 Publication Model: Print-Electronic Cited

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Academic Journal

Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study.

  • Authors : Alonso A; Rheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain; Department of Enginyeria de Sistemes, Automática i Informàtica Industrial, Polytechnic University of Catalonia, Barcelona, Spain.

Subjects: Antigens, CD/Antigens, CD/Antigens, CD/*genetics ; Cell Adhesion Molecules, Neuronal/Cell Adhesion Molecules, Neuronal/Cell Adhesion Molecules, Neuronal/*genetics ; Chloride Channels/Chloride Channels/Chloride Channels/*genetics

  • Source: Gastroenterology [Gastroenterology] 2015 Apr; Vol. 148 (4), pp. 794-805. Date of Electronic Publication: 2014 Dec 31.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print-Electronic Cited

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Academic Journal

Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.

Subjects: Polymorphism, Single Nucleotide*; Autoimmunity/Autoimmunity/Autoimmunity/*genetics ; Hepatitis, Autoimmune/Hepatitis, Autoimmune/Hepatitis, Autoimmune/*genetics

  • Source: Gastroenterology [Gastroenterology] 2014 Aug; Vol. 147 (2), pp. 443-52.e5. Date of Electronic Publication: 2014 Apr 23.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print-Electronic Cited

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Academic Journal

Germline mutations in oncogene-induced senescence pathways are associated with multiple sessile serrated adenomas.

Subjects: Germ-Line Mutation*; Adenomatous Polyps/Adenomatous Polyps/Adenomatous Polyps/*genetics ; Cellular Senescence/Cellular Senescence/Cellular Senescence/*genetics

  • Source: Gastroenterology [Gastroenterology] 2014 Feb; Vol. 146 (2), pp. 520-9.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print Cited Medium:

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Academic Journal

Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.

Subjects: Polymorphism, Single Nucleotide*; Cardiovascular Diseases/Cardiovascular Diseases/Cardiovascular Diseases/*genetics ; Renal Insufficiency, Chronic/Renal Insufficiency, Chronic/Renal Insufficiency, Chronic/*genetics

  • Source: American journal of kidney diseases : the official journal of the National Kidney Foundation [Am J Kidney Dis] 2013 Jun; Vol. 61 (6), pp. 889-98. Date of Electronic Publication: Publisher: W.B. Saunders Country of Publication: United States NLM ID: 8110075 Publication Model: Print-Electronic Cited

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  • 1-10 of  75 results for ""Adaptor Proteins, Signal Transducing""