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Lipid-lowering drugs -- See Antilipemic agents


  1
 

Lipid membranes -- See Also the narrower term Bilayer lipid membranes


  1
Lipid membranes.   9
Lipid membranes -- Biotechnology. : The giant vesicle book / edited by Rumiana Dimova, Carlos M. Marques  2020 1
 

Lipid metabolism -- See Lipids Metabolism


  1
Lipid Metabolism   63
 

Lipid Metabolism Disorder -- See Lipid Metabolism Disorders


Pathological conditions resulting from abnormal anabolism or catabolism of lipids in the body
  1
 

Lipid metabolism disorders -- See Lipids Metabolism Disorders


  1
Lipid Metabolism Disorders   5
Lipid Metabolism Disorders -- therapy : Evidence-based management of lipid disorders / Maud N. Vissers, John J.P. Kastelein, Erik S. Stroes, [editors]  2010 1
Lipid Metabolism -- genetics : Cardioskeletal myopathies in children and young adults / edited by John Lynn Jefferies, Burns C. Blaxall, Jeffrey Robbins, Jeffrey A. Towbin  2017 1
Lipid Metabolism, Inborn Errors : Therapeutic lipidology / edited by Michael H. Davidson, Peter P. Toth, Kevin C. Maki ; foreword by Antonio M. Gotto Jr  2007 1
Lipid Metabolism -- physiology   2
Lipid oxidation   3
Lipid Peroxidation : Reactive oxygen species : methods and protocols / edited by Jesús Espada  2021 1
Lipid Peroxidation -- physiology : Oxidants, antioxidants, and free radicals / edited by Steven I. Baskin and Harry Salem  1997 1
 

Lipid Peroxidations -- See Lipid Peroxidation


Peroxidase catalyzed oxidation of lipids using hydrogen peroxide as an electron acceptor
  1
Lipid Peroxides : Lipid hydroperoxide-derived modification of biomolecules / Yoji Kato, editor  2014 1
 

Lipid research -- See Lipids Research


  1
 

Lipid storage diseases -- See Lipidoses


  1
 

Lipid storage disorders -- See Lipidoses


  1
 

Lipid synthesis -- See Lipids Synthesis


  1
Lipide   8
lipide insecte : Insect lipids : chemistry, biochemistry, and biology / edited by David W. Stanley-Samuelson and Dennis R. Nelson  1993 1
 

Lipidemia -- See Hyperlipidemias


Conditions with excess LIPIDS in the blood
  1
 

Lipidemias -- See Hyperlipidemias


Conditions with excess LIPIDS in the blood
  1
Lipiden.   4
Lipídeos.   2
Lipídeos (análise;fisiologia;metabolismo) : Membrane microdomain signaling : lipid rafts in biology and medicine / edited by Mark P. Mattson  2005 1
 

Lipides -- See Lipids


  1
Lipides.   2
Lipides -- Analyse. : Lipid analysis / F.W. Hemming, J.N. Hawthorne  1996 1
Lipides des membranes. : Lipid signaling protocols / Banafshé Larijani, editor ; Rudiger Woscholski, editor ; Colin A. Rosser, editor  2009 1
Lipides membranaires. : Protein-lipid interactions : new approaches and emerging concepts / C. Reyes Mateo [and others] (eds.)  2006 1
Lipides -- Métabolisme. : Lipids and the kidney / volume editors, W.F. Keane, W. Hörl, B.L. Kasiske  1997 1
Lipidios.   3
Lipidios (metabolismo) : Brain development : relationship to dietary lipid and lipid metabolism / Jacqueline Jumpsen and Michael T. Clandinin  1995 1
Lipidmembran : Generic and specific roles of saccharides at cell and bacteria surfaces : revealed by specular and off-specular x-ray and neutron scattering / Emanuel Schneck  2011 1
 

Lipidoses -- See Also the narrower term Sphingolipidoses


  1
Lipidoses.   2
 

Lipidoses, Glucosyl Cerebroside -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Lipidoses, Glucosylceramide -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
Lipidoses -- metabolism : Lipids and the kidney / volume editors, W.F. Keane, W. Hörl, B.L. Kasiske  1997 1
 

Lipidosis -- See Lipidoses


  1
 

Lipidosis, Glucosyl Cerebroside -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Lipidosis, Glucosylceramide -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Lipidosis, Hereditary Dystopic -- See Fabry Disease


An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders
  1
 

Lipidosis Syndrome, Cerebroside -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Lipidosis Syndromes, Cerebroside -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
  Lipids -- 18 Related Subjects   18
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