Robert M. Tanguay – författare
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7 produkter
Big Book on Small Heat Shock Proteins
Av Robert M. Tanguay, Lawrence E. Hightower
Inbunden, 2015
2253 kr
Lägg i varukorg
Based upon a workshop entitled “The Small HSP World” held in Québec 2-5 October 2014. Twenty-five scientists provided chapters for the book. The chapters are from the best scientists currently working in this field. These colleagues include Arrigo, Benesch, Benjamin, Buchner-Haslbeck-Weinkauf, …
Big Book on Small Heat Shock Proteins
Av Lawrence E. Hightower, Robert M. Tanguay
E-bok, 2015
2174 kr
Lägg i varukorg
Based upon a workshop entitled “The Small HSP World” held in Québec 2-5 October 2014. Twenty-five scientists provided chapters for the book. The chapters are from the best scientists currently working in this field. These colleagues include Arrigo, Benesch, Benjamin, Buchner-Haslbeck-Weinkauf, …
Big Book on Small Heat Shock Proteins
Av Robert M. Tanguay, Lawrence E. Hightower
Häftad, 2016
1687 kr
Lägg i varukorg
Based upon a workshop entitled “The Small HSP World” held in Québec 2-5 October 2014. Twenty-five scientists provided chapters for the book. The chapters are from the best scientists currently working in this field. These colleagues include Arrigo, Benesch, Benjamin, Buchner-Haslbeck-Weinkauf, …
Hereditary Tyrosinemia
Pathogenesis, Screening and Management
Inbunden, 2017
1861 kr
Lägg i varukorg
Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH). The worldwide frequency of HT1 is one per 100,000 births, but some regions have a significantly higher incidence (1:1,800). The FAH …
Hereditary Tyrosinemia
Pathogenesis, Screening and Management
E-bok, 2017
2437 kr
Lägg i varukorg
Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH). The worldwide frequency of HT1 is one per 100,000 births, but some regions have a significantly higher incidence (1:1,800). The FAH …
Hereditary Tyrosinemia
Pathogenesis, Screening and Management
Häftad, 2018
1766 kr
Lägg i varukorg
Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH). The worldwide frequency of HT1 is one per 100,000 births, but some regions have a significantly higher incidence (1:1,800). The FAH …
Aging, Cancer and Age-related Disease
Common Mechanisms?, Volume 1197
Häftad, 2010
1122 kr
Tillfälligt slut
This volume recognizes the rapidly expanding research linking aging, age-related diseases, and the delicate balance between neurodegeneration and cancer. Wide perspectives on aging are covered, ranging from metabolic and cellular interventions in aging, oxidative stress resistance, protein folding …
