Search Results - "Daenzer, M"

Drosophila melanogaster Models of Galactosemia by Daenzer, J M I, Fridovich-Keil, J L

“…The galactosemias are a family of autosomal recessive genetic disorders resulting from impaired function of the Leloir pathway of galactose metabolism. Type I,…”
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UDP-galactose 4'-epimerase activities toward UDP-Gal and UDP-GalNAc play different roles in the development of Drosophila melanogaster by Daenzer, Jennifer M I, Sanders, Rebecca D, Hang, Darwin, Fridovich-Keil, Judith L

“…In both humans and Drosophila melanogaster, UDP-galactose 4'-epimerase (GALE) catalyzes two distinct reactions, interconverting UDP-galactose (UDP-gal) and…”
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Acute and long-term outcomes in a Drosophila melanogaster model of classic galactosemia occur independently of galactose-1-phosphate accumulation by Daenzer, Jennifer M I, Jumbo-Lucioni, Patricia P, Hopson, Marquise L, Garza, Kerry R, Ryan, Emily L, Fridovich-Keil, Judith L

“…Classic galactosemia (CG) is a potentially lethal inborn error of metabolism that results from the profound loss of galactose-1-phosphate uridylyltransferase…”
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Restoring galactose metabolism without restoring GALT rescues both compromised survival in larvae and an adult climbing deficit in a GALT‐null D. Melanogaster model of classic galactosemia by Daenzer, Jennifer M. I., Druss, Jared J., Fridovich‐Keil, Judith L.

“…Classic galactosemia (CG) is an autosomal recessive disorder that results from profound deficiency of galactose‐1‐phosphate uridylyltransferase (GALT), the…”
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Neonatal GALT gene replacement offers metabolic and phenotypic correction through early adulthood in a rat model of classic galactosemia by Daenzer, Jennifer M. I., Rasmussen, Shauna A., Patel, Sneh, McKenna, James, Fridovich‐Keil, Judith L.

“…Classic galactosemia (CG) results from profound deficiency of galactose‐1‐P uridylyltransferase (GALT). Despite early detection by newborn screening and…”
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A pilot study of neonatal GALT gene replacement using AAV9 dramatically lowers galactose metabolites in blood, liver, and brain and minimizes cataracts in GALT‐null rat pups by Rasmussen, Shauna A., Daenzer, Jennifer M. I., Fridovich‐Keil, Judith L.

“…Classic galactosemia (CG) is a rare metabolic disorder that results from profound deficiency of galactose‐1‐P uridylyltransferase (GALT). Despite early…”
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A galactose‐1‐phosphate uridylyltransferase‐null rat model of classic galactosemia mimics relevant patient outcomes and reveals tissue‐specific and longitudinal differences in galactose metabolism by Rasmussen, Shauna A., Daenzer, Jennifer M. I., MacWilliams, Jessica A., Head, S. Taylor, Williams, Martine B., Geurts, Aron M., Schroeder, Jason P., Weinshenker, David, Fridovich‐Keil, Judith L.

“…Classic galactosemia (CG) is a potentially lethal inborn error of metabolism, if untreated, that results from profound deficiency of galactose‐1‐phosphate…”
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Prenatal high protein exposure decreases energy expenditure and increases adiposity in young rats by Daenzer, Maren, Ortmann, Sylvia, Klaus, Susanne, Metges, Cornelia C

“…Epidemiologic results suggest that protein intake in infancy and later adiposity might be related. We examined whether high dietary protein exposure in utero…”
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Whole-body nitrogen and splanchnic amino acid metabolism differ in rats fed mixed diets containing casein or its corresponding amino acid mixture by Daenzer, M, Petzke, K J, Bequette, B J, Metges, C C

“…Whole-body and splanchnic metabolism of dietary amino acids derived from casein (CAS) or the corresponding crystalline L-amino acid mixture (AA) were compared…”
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13C Gas Chromatography–Combustion Isotope Ratio Mass Spectrometry Analysis of N-Pivaloyl Amino Acid Esters of Tissue and Plasma Samples by Metges, Cornelia C., Daenzer, Maren

“…We present the analysis of the stable carbon isotope compositions of 14 individual N-pivaloyl-isopropyl (NPP) amino acid esters by gas…”
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Low-abundance plasma and urinary [15N]urea enrichments analyzed by gas chromatography/combustion/isotope ratio mass spectrometry by Metges, Cornelia C., Daenzer, Maren, Petzke, Klaus J., Elsner, Angelika

“…We report a method for determining plasma und urinary [15N]urea enrichments in an abundance range between 0.37 and 0.52 15N atom% (0–0.15 atom% excess (APE)…”
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Improved in vitro stability of serum osteocalcin by using a new commercially available antiproteolytic compound by Baumgrass, Ria, Daenzer, Maren, Felsenberg, Dieter

“…The effect of a commercially available antiproteolytic compound (OSCAstabil) on the degradation in vitro of serum osteocalcin (Oc) was investigated in serum…”
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Maid in the Market: Women's Paid Domestic Labour by Daenzer, Patricia M.

“…The broadened scope of discussions, linking conditions common to a variety of female-dominated jobs through related strands of analyses, makes the work unique…”
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The Atlanta Paradox: A Volume in the Multi-City Study of Urban Inequality by Daenzer, Patricia M.

“…"The Atlanta Paradox: A Volume in the Multi-City Study of Urban Inequality" edited by David L. Sjoquist is reviewed…”
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Social welfare in global context. James Midgley. London, Sage, 1997 by Daenzer, P. M.

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Social welfare in global context by Daenzer, P M, Midgley, James

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P1‐059: ENGULFMENT ADAPTER PTB DOMAIN CONTAINING 1 (GULP1) FORMS DIMERS IN VIVO, AND DIMERIZATION IS FURTHER PROMOTED BY AMYLOID PRECURSOR PROTEIN (APP) by Wahler, Anke, Schnack, Cathrin, Einem, Bjoern, Danzer, Karin M., Arnim, Christine A.F.

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ENGULFMENT ADAPTER PTB DOMAIN CONTAINING 1 (GULP1) FORMS DIMERS IN VIVO, AND DIMERIZATION IS FURTHER PROMOTED BY AMYLOID PRECURSOR PROTEIN (APP) by Wahler, Anke, Schnack, Cathrin, von Einem, Bjoern, Danzer, Karin M, von Arnim, Christine A.F

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UNEMPLOYMENT AND MINORITY IMMIGRANTS IN CANADA by Daenzer, Patricia

“…This paper explores the labour-market status and experience of racial minorities in Canada, and examines and criticises labour-market policy which ignores the…”
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Sjoquist, David L. (ed.). "The Atlanta Paradox: A Volume in the Multi-City Study of Urban Inequality" (Book Review) by Daenzer, Patricia M

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