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Lipids, Single cell -- See Single cell lipids


  1
Lipids -- Spectra.   3
Lipids -- Study and teaching : Teaching innovations in lipid science / edited by Randall J. Weselake  2008 1
Lipids -- Synthesis.   6
Lipids -- Tables : Handbook of Lipid Bilayers / Derek Marsh  2013 1
Lipids -- Therapeutic use.   3
Lipids -- toxicity. : Obesity and lipotoxicity / Ayse Basak Engin, Atilla Engin, editors  2017 1
Lipidstoffwechselstörung : Adipositas, Diabetes und Fettstoffwechselstörungen im Kindesalter / Thomas Danne, Olga Kordonouri  2016 1
 

Lipiner, Sigfrido, 1856-1911 -- See Lipiner, Siegfried, 1856-1911


  1
 

Lipins -- See Lipids


  1
 

Lipitsa horse -- See Lipizzaner horse


  1
 

Lipman, Yom Ṭov, 1579-1654 -- See Heller, Yom Tov Lipmann ben Nathan ha-Levi ben Wallerstein, 1579-1654


  1
 

Lipo-sculpture -- See Liposculpture


Here are entered works on body contouring using liposuction as well as injections of fat. Works on the removal of subcutaneous fat using suction are entered under Liposuction
  1
 

Lipocaic -- See Lipotropic Agents


Endogenous factors or drugs that increase the transport and metabolism of LIPIDS including the synthesis of LIPOPROTEINS by the LIVER and their uptake by extrahepatic tissues
  1
 

Lipocephala -- See Bivalves


  1
 

Lipochromes -- See Carotenoids


  1
 

Lipofuscin -- See Lipofuscins


  1
Lipofuscin -- physiology.   2
 

Lipofuscin Storage Disease -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Lipofuscin Storage Diseases -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Lipofuscinoses, Neuronal ceroid -- See Neuronal ceroid-lipofuscinoses


  1
 

Lipofuscinosis, Neuronal Ceroid -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
Lipofuscins.   4
Lipogenesis.   2
 

Lipoglycan Receptor -- See Lipopolysaccharide Receptors


Glycolipid-anchored membrane glycoproteins expressed on cells of the myelomonocyte lineage including MONOCYTES; MACROPHAGES; and some GRANULOCYTES. They function as receptors for the complex of lipopolysaccharide (LPS) and LPS-binding protein
  1
 

Lipoglycans -- See Lipopolysaccharides


Lipid-containing polysaccharides which are endotoxins and important group-specific antigens. They are often derived from the cell wall of gram-negative bacteria and induce immunoglobulin secretion. The lipopolysaccharide molecule consists of three parts: LIPID A, core polysaccharide, and O-specific chains (O ANTIGENS). When derived from Escherichia coli, lipopolysaccharides serve as polyclonal B-cell mitogens commonly used in laboratory immunology. (From Dorland, 28th ed)
  1
 

Lipoic Acid -- See Thioctic Acid


An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS
  1
Lipoic acid. : Lipoic acid : energy production, antioxidant activity and health effects / edited by Mulchand S. Patel and Lester Packer  2008 1
Lipoic acid -- Health aspects. : Lipoic acid : energy production, antioxidant activity and health effects / edited by Mulchand S. Patel and Lester Packer  2008 1
Lipoic acid -- Physiological effect. : Lipoic acid in health and disease / edited by Jürgen Fuchs, Lester Packer, Guido Zimmer  1997 1
Lipoic acid -- Therapeutic use.   2
 

Lipoid Histiocytoses (Kerasin Type) -- 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
 

Lipoid Histiocytosis (Kerasin Type) -- 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
 

Lipoidoses, Kerasin -- 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
 

Lipoidosis -- See Lipidoses


  1
 

Lipoidosis, Kerasin -- 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
 

Lipoids -- See Lipids


  1
 

Lipolysis, Aspiration -- See Lipectomy


Removal of localized SUBCUTANEOUS FAT deposits by SUCTION CURETTAGE or blunt CANNULATION in the cosmetic correction of OBESITY and other esthetic contour defects
  1
 

Lipolysis, Suction -- See Lipectomy


Removal of localized SUBCUTANEOUS FAT deposits by SUCTION CURETTAGE or blunt CANNULATION in the cosmetic correction of OBESITY and other esthetic contour defects
  1
 

lipolyticas, Yarrowia -- See Yarrowia


A genus of ascomycetous yeast in the family Dipodascaceae, order SACCHAROMYCETALES
  1
 

Liponsaure-ratiopharm -- See Thioctic Acid


An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS
  1
 

Liponsaureratiopharm -- See Thioctic Acid


An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS
  1
 

Lipophile-hydrophile balance -- See Hydrophile-lipophile balance


  1
 

Lipophilic surfaces -- See Hydrophobic surfaces


  1
 

Lipoplasties -- See Lipectomy


Removal of localized SUBCUTANEOUS FAT deposits by SUCTION CURETTAGE or blunt CANNULATION in the cosmetic correction of OBESITY and other esthetic contour defects
  1
 

Lipoplasty -- See Lipectomy


Removal of localized SUBCUTANEOUS FAT deposits by SUCTION CURETTAGE or blunt CANNULATION in the cosmetic correction of OBESITY and other esthetic contour defects
  1
 

Lipoplasty, Suction -- See Liposuction


Here are entered works on the removal of subcutaneous fat using suction. Works on body contouring using liposuction as well as injections of fat are entered under Liposculpture
  1
Lipopolysaccharide Receptors. : CD14 in the inflammatory response / volume editor, Robert S. Jack  2000 1
Lipopolysaccharides.   2
Lipopolysaccharides -- metabolism. : The role of bacterial carbohydrates in microbe-plant interactions : Rhizobium-legume nitrogen-fixing symbiosis / Russell W. Carlson  2012 1
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