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Peroxisomal diseases -- See Peroxisomal disorders


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Peroxisomal Disorder -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
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Peroxisomal disorders   2
Peroxisomal Disorders -- genetics : Peroxisome biology : experimental models, peroxisomal disorders and neurological diseases / Gérard Lizard, editor  2020 1
Peroxisomal disorders -- Periodicals : PPAR research (Online)  2006- 1
 

Peroxisomal Dysfunction, General -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
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Peroxisomal Dysfunction, Multiple -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
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Peroxisomal Dysfunction, Single -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
  1
 

Peroxisomal Dysfunctions, General -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
  1
 

Peroxisomal Dysfunctions, Multiple -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
  1
 

Peroxisomal Dysfunctions, Single -- See Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
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Peroxisome -- See Peroxisomes


Microbodies which occur in animal and plant cells and in certain fungi and protozoa. They contain peroxidase, catalase, and allied enzymes. (From Singleton and Sainsbury, Dictionary of Microbiology and Molecular Biology, 2nd ed)
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Peroxisome Proliferator-Activated Receptors   2
Peroxisome Proliferator-Activated Receptors -- therapeutic use : Inflammation in heart failure / edited by Matthijs Blankesteijn and Raffaele Altara  2015 1
  Peroxisome Proliferators -- 2 Related Subjects   2
 

Peroxisomes -- See Also Peroxisomal Disorders


A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
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Peroxisomes.   8
 

Peroxisomes Diseases -- See Peroxisomal disorders


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Peroxisomes -- Laboratory manuals   3
Peroxisomes -- Periodicals : PPAR research (Online)  2006- 1
Peroxisomes -- Receptors : Peroxisome proliferator-activated receptors : discovery and recent advances / Jihan A. Youssef, Mostafa Z. Badr  2013 1
 

Peroxonitrite -- See Peroxynitrite


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Peroxy compounds -- See Peroxides


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Peroxynitrate -- See Peroxynitrite


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Peroxynitrite. : Peroxynitrite detection in biological media : challenges and advances / editors: Serban Peteu, Sabine Szunerits, Mekki Bayachou  2015 1
 

Peroxynitrosyl -- See Peroxynitrite


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Peroxynitrous acid -- See Peroxynitrite


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Peroxynitrous Acid : Peroxynitrite detection in biological media : challenges and advances / editors: Serban Peteu, Sabine Szunerits, Mekki Bayachou  2015 1
 

Peroxysoma -- See Peroxisomes


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Peroxysomal disorders -- See Peroxisomal disorders


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Peroxysomen. : Peroxisomes : biology and importance in toxicology and medicine / edited by Gordon Gibson and Brian Lake  1993 1
Perón, Eva, 1919-1952 : Evita [documentary] / written and directed by Eduardo Montes-Bradley ; produced by Soledad Liendo  2013 1
Perpendicular angles and Supplementary angles : Schaum's Geometry Supplementary Problem 1.10 / David Rader  c2012 1
Perpendicular Bisectors : Schaum's Calculus Supplementary Problem 3.21 Video Solution / David Rader  c2011 1
 

Perpendicular gardening -- See Vertical gardening


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Perpetua, Saint, -203.   7
 

Perpetual almanacs -- See Perpetual calendars


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Perpetual calendars. : Dewitt's 200 year calendar and book of horoscopes  1999 1
Perpetual motion. : Retouches / Director: Schwizgebel, Georges  2009 1
Perpetual motion -- History.   2
Perpetual Trustees Australia -- Periodicals : Annual report / Perpetual Trustees Australia Limited  1964- 1
 

Perpetually frozen ground -- See Permafrost


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Perpétue, Saint, -203 -- See Perpetua, Saint, -203


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  Perpetuities -- 2 Related Subjects   2
Perpetuities   24
[Perpetuities Act 1984 (NSW)] Australia : The Perpetuities Act 1984 / by C.M. Sappideen and P.J. Butt  1986 1
Perpetuities -- Australia -- New South Wales. : The Perpetuities Act 1984 / by C.M. Sappideen and P.J. Butt  1986 1
Perpetuities -- Great Britain   9
Perpetuities -- Great Britain -- Early works to 1800 : The law concerning estates taile : and remainders and reversions expectant thereupon, illustrated. The Statute De Donis Conditionalibus, and what Estates of Inheritance may be Intailed, and what may not be Intailed: With the Conveniencies and Inconveniencies arising thereby, Explained and Demonstrated. The doctrine of perpetuities fully cleared. And the Nature, Operation, and Use of Fines, in destroying of Estates Taile, and of Recoveries in Barring Remainders and Reversions, Approved. With Variety of Authentick Precedents, and Select Cases proper to each Particular, and General Cases Applicable to the whole / by H. Curson of the Inner Temple  1703 1
Perpetuities -- India : The law of perpetuities in British India / by Asutosh Mukhopadhyay  1902 1
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