Cary O. Hard: search on Z-Library

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1

State-of-the-Art 2019 on Gene therapy for Phenylketonuria

Grisch-Chan, Hiu Man, Schwank, Gerald, Harding, Cary O, Thony, Beat

Journal:

Human Gene Therapy

Year:

2019

Language:

english

File:

PDF, 386 KB

english, 2019

2

Aluminum Toxicity

Gilbert-Barness, Enid, Barness, Lewis A., Wolff, Jon, Harding, Cary

Journal:

Archives of Pediatrics and Adolescent Medicine

Year:

1998

Language:

english

File:

PDF, 146 KB

english, 1998

3

Tetrahydrobiopterin treatment reduces brain L-Phe but only partially improves serotonin in hyperphenylalaninemic ENU1/2 mice

Scherer, Tanja, Allegri, Gabriella, Sarkissian, Christineh N., Ying, Ming, Grisch-Chan, Hiu Man, Rassi, Anahita, Winn, Shelley R., Harding, Cary O., Martinez, Aurora, Thöny, Beat

Journal:

Journal of Inherited Metabolic Disease

Year:

2018

Language:

english

File:

PDF, 815 KB

english, 2018

4

Functional methionine synthase deficiency due to cblG disorder: A report of two patients and a review

Harding, Cary O., Arnold, Georgianne, Barness, Lewis A., Wolff, Jon A., Rosenblatt, David S.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 71 KB

english, 1997

5

Advances and challenges in phenylketonuria

Cary O. Harding, Nenad Blau

Journal:

Journal of Inherited Metabolic Disease

Year:

2010

Language:

english

File:

PDF, 101 KB

english, 2010

6

Normal vitamin D levels and bone mineral density among children with inborn errors of metabolism consuming medical food–based diets

Geiger, Katie E., Koeller, David M., Harding, Cary O., Huntington, Kathleen L., Gillingham, Melanie B.

Journal:

Nutrition Research

Year:

2016

Language:

english

File:

PDF, 482 KB

english, 2016

7

Long-term survival in typical thanatophoric dysplasia type 1

Baker, Kristin M., Olson, David S., Harding, Cary O., Pauli, Richard M.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 2.07 MB

english, 1997

8

Prevalence and Distribution of the c.1436C→T Sequence Variant of Carnitine Palmitoyltransferase 1A among Alaska Native Infants

Bradford D. Gessner, Melanie B. Gillingham, Monique A. Johnson, C. Sue Richards, William E. Lambert, David Sesser, Leanne C. Rien, Cheryl A. Hermerath, Michael R. Skeels, Stephanie Birch, Cary O. Hard

Journal:

The Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 546 KB

english, 2011

9

Undergraduate course in environmental design and manufacturing

Andrew S. Borchers, Trevor Harding, Terri Lynch-Caris, Benjamin Redekop, Craig Hof, Jackie El-Sayed, Daryl Doyle

Journal:

Journal of Manufacturing Systems

Year:

2005

Language:

english

File:

PDF, 633 KB

english, 2005

10

Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency

Melanie B. Gillingham, Richard G. Weleber, Martha Neuringer, William E. Connor, Monte Mills, Sandy van Calcar, James ver Hoeve, Jon Wolff, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 354 KB

english, 2005

11

Molecular Basis of Two-Exon Skipping (Exons 12 and 13) by c.1248+5g>a in OXCT1 Gene: Study on Intermediates of OXCT1 Transcripts in Fibroblasts

Hori, Tomohiro, Fukao, Toshiyuki, Murase, Keiko, Sakaguchi, Naomi, Harding, Cary O., Kondo, Naomi

Journal:

Year:

2013

Language:

english

File:

PDF, 443 KB

english, 2013

12

In Vivo Selection of Transplanted Hepatocytes by Pharmacological Inhibition of Fumarylacetoacetate Hydrolase in Wild-type Mice

Paulk, Nicole K, Wursthorn, Karsten, Haft, Annelise, Pelz, Carl, Clarke, Gregory, Newell, Amy H, Olson, Susan B, Harding, Cary O, Finegold, Milton J, Bateman, Raymond L, Witte, John F, McClard, Ronald

Journal:

Molecular Therapy

Year:

2012

Language:

english

File:

PDF, 1.72 MB

english, 2012

13

sar: A Genetic Mouse Model for Human Sarcosinemia Generated by Ethylnitrosourea Mutagenesis

Cary O. Harding, Phillip Williams, Denise M. Pflanzer, Robert E. Colwell, Paul W. Lyne and Jon A. Wolff

Journal:

Proceedings of the National Academy of Sciences

Year:

1992

Language:

english

File:

PDF, 1010 KB

english, 1992

14

Spectrum of ocular manifestations in cobalamin C and cobalamin A types of methylmalonic acidemia

Ku, Cristy A., Ng, Jacqueline K., Karr, Daniel J., Reznick, Leah, Harding, Cary O., Weleber, Richard G., Pennesi, Mark E.

Journal:

Ophthalmic Genetics

Year:

2016

Language:

english

File:

PDF, 1.32 MB

english, 2016

15

355. Minicircles Show Improved Hepatic Expression of Their Transgene from a Natural Endogenous Promoter and Are Lost Upon Partial Hepatectomy Due to the Episomal Nature of the Vector

Viecelli, Hiu-Man, Schlegel, Andrea, Scherer, Tanja, Allegri, Gabirella, Schleef, Martin, Harding, Cary O, Häberle, Johannes, Thöny, Beat

Journal:

Molecular Therapy

Year:

2016

Language:

english

File:

PDF, 328 KB

english, 2016

16

Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene

Paul J. Isackson, Heather Bujnicki, Cary O. Harding, Georgirene D. Vladutiu

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 255 KB

english, 2005

17

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

Georgianne L. Arnold, Johan Van Hove, Debra Freedenberg, Arnold Strauss, Nicola Longo, Barbara Burton, Cheryl Garganta, Can Ficicioglu, Stephen Cederbaum, Cary Harding, Richard G. Boles, Dietrich Mate

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 171 KB

english, 2009

18

Comparison of Adeno-Associated Virus Pseudotype 1, 2, and 8 Vectors Administered by Intramuscular Injection in the Treatment of Murine Phenylketonuria

Rebuffat, Alexandre, Harding, Cary O., Ding, Zhaobing, Thöny, Beat

Journal:

Human Gene Therapy

Year:

2010

Language:

english

File:

PDF, 2.15 MB

english, 2010

19

Pegvaliase for the treatment of phenylketonuria: A pivotal, double-blind randomized discontinuation Phase 3 clinical trial

Harding, Cary O., Stephen Amato, R., Stuy, Mary, Longo, Nicola, Burton, Barbara K., Posner, John, Weng, Haoling H., Merilainen, Markus, Gu, Zhonghua, Jiang, Joy, Vockley, Jerry

Journal:

Molecular Genetics and Metabolism

Year:

2018

Language:

english

File:

PDF, 980 KB

english, 2018

20

Prospects for Cell-Directed Curative Therapy of Phenylketonuria (PKU)

Harding, Cary O.

Journal:

Molecular Frontiers Journal

Year:

2019

Language:

english

File:

PDF, 962 KB

english, 2019

21

SPIE Proceedings [SPIE SPIE Defense and Security Symposium - Orlando, FL (Sunday 16 March 2008)] Head- and Helmet-Mounted Displays XIII: Design and Applications - Safety qualification and operational assessment of a night vision cueing and display system

Barnaba, James M., Wilson, Cary W., Baez-Vazquez, Melina, Brown, Randall W., Marasco, Peter L., Harding, Thomas H., Jennings, Sion A.

Year:

2008

Language:

english

File:

PDF, 1.52 MB

english, 2008

22

Leigh syndrome in an infant resulting from mitochondrial DNA depletion

Michael J Absalon, Cary O Harding, Daniel R Fain, Lei Li, Kenneth J Mack

Journal:

Pediatric Neurology

Year:

2001

Language:

english

File:

PDF, 146 KB

english, 2001

23

[ACM Press Working group reports from ITiCSE - Aarhus, Denmark (2002.06.24-2002.06.28)] Working group reports from ITiCSE on Innovation and technology in computer science education - ITiCSE-WGR '02 - Addressing student cheating

Dick, Martin, Sheard, Judy, Bareiss, Cathy, Carter, Janet, Joyce, Donald, Harding, Trevor, Laxer, Cary

Year:

2002

Language:

english

File:

PDF, 316 KB

english, 2002

24

New era in treatment for phenylketonuria: Pharmacologic therapy with sapropterin dihydrochloride

Journal:

Biologics Targets & Therapy

Year:

2010

Language:

english

File:

PDF, 181 KB

english, 2010

25

The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuria

Cary O Harding, Mark Neff, Krzysztof Wild, Kelly Jones, Lina Elzaouk, Beat Thöny, Sheldon Milstien

Journal:

Molecular Genetics and Metabolism

Year:

2004

Language:

english

File:

PDF, 186 KB

english, 2004

26

Substrate oxidation and cardiac performance during exercise in disorders of long chain fatty acid oxidation

Annie M. Behrend, Cary O. Harding, James D. Shoemaker, Dietrich Matern, David J. Sahn, Diane L. Elliot, Melanie B. Gillingham

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 469 KB

english, 2012

27

Hand it to the skin in Costello syndrome

Angela Lin, Cary Harding, Michael Silberbach

Journal:

The Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

28

Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controls

Sailer, Melissa, Elizondo, Gabriela, Martin, Julie, Harding, Cary O., Gillingham, Melanie B.

Journal:

Molecular Genetics and Metabolism Reports

Year:

2020

File:

PDF, 835 KB

2020

29

A Sensitive Assay System To Test Antisense Oligonucleotides for Splice Suppression Therapy in the Mouse Liver

Gallego-Villar, Lorena, Viecelli, Hiu Man, Pérez, Belén, Harding, Cary O, Ugarte, Magdalena, Thöny, Beat, Desviat, Lourdes R

Journal:

Molecular Therapy — Nucleic Acids

Year:

2014

Language:

english

File:

PDF, 1.64 MB

english, 2014

30

High dose sapropterin dihydrochloride therapy improves monoamine neurotransmitter turnover in murine phenylketonuria (PKU)

Winn, Shelley R., Scherer, Tanja, Thöny, Beat, Harding, Cary O.

Journal:

Molecular Genetics and Metabolism

Year:

2016

Language:

english

File:

PDF, 765 KB

english, 2016

31

Higher Dietary Protein Intake preserves lean body mass, lowers liver lipid deposition, and maintains metabolic control in participants with long‐chain fatty acid oxidation disorders

Gillingham, Melanie B., Elizondo, Gabriela, Behrend, Annie, Matern, Dietrich, Schoeller, Dale A., Harding, Cary O., Purnell, Jonathan Q.

Journal:

Journal of Inherited Metabolic Disease

Year:

2019

Language:

english

File:

PDF, 2.33 MB

english, 2019

32

A novel Pah-exon1 deleted murine model of phenylalanine hydroxylase (PAH) deficiency

Richards, Daelyn Y., Winn, Shelley R., Dudley, Sandra, Fedorov, Lev, Rimann, Nicole, ThÃ¶ny, Beat, Harding, Cary O.

Journal:

Molecular Genetics and Metabolism

Year:

2020

File:

PDF, 6.35 MB

2020

33

404. Therapeutic Correction of PKU in a Mouse Model by Ectopic Expression of PAH and Its BH4- Cofactor Genes in Skeletal Muscle by a Recombinant Triple-Cistronic AAV2-Based Pseudotype 1 Vector

Ding, Zhaobing, O. Harding, Cary, Rebuffat, Alexandre, Elzaouk, Lina, Wolff, Jon A., Thony, Beat

Journal:

Molecular Therapy

Year:

2006

Language:

english

File:

PDF, 95 KB

english, 2006

34

Glutathione in blood and its utilization in milk secretion.

Harding, T. S., Cary, C. A.

Journal:

Experimental Biology and Medicine

Year:

1926

Language:

english

File:

PDF, 275 KB

english, 1926

35

146. Optimizing Safety and Long-Term Efficacy of Liver Gene Therapy With Non-Integrating Naked-DNA Minicircle Vectors Expressing Their Transgene from a Natural Promoter

Man Viecelli, Hiu, Schlegel, Andrea, Scherer, Tanja, Schleef, Martin, Harding, Cary O., Thöny, Beat

Journal:

Molecular Therapy

Year:

2015

Language:

english

File:

PDF, 360 KB

english, 2015

36

Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma

Cary O. Harding, Roberta A. Pagon

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 502 KB

english, 1990

37

Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency

Melanie B. Gillingham, Jonathan Q. Purnell, Julia Jordan, Diane Stadler, Andrea M. Haqq, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 285 KB

english, 2007

38

Next generation deep sequencing corrects diagnostic pitfalls of traditional molecular approach in a patient with prenatal onset of Pompe disease

Tsai, Anne Chun-Hui, Hung, Yu-Wen, Harding, Cary, Koeller, David M., Wang, Jing, Wong, Lee-Jun C.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 2.93 MB

english, 2017

39

Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice

Winn, Shelley R., Scherer, Tanja, Thöny, Beat, Ying, Ming, Martinez, Aurora, Weber, Sydney, Raber, Jacob, Harding, Cary O.

Journal:

Molecular Genetics and Metabolism

Year:

2017

Language:

english

File:

PDF, 1.41 MB

english, 2017

40

Association of immune response with efficacy and safety outcomes in adults with phenylketonuria administered pegvaliase in phase 3 clinical trials

Gupta, Soumi, Lau, Kelly, Harding, Cary O., Shepherd, Gillian, Boyer, Ryan, Atkinson, John P., Knight, Vijaya, Olbertz, Joy, Larimore, Kevin, Gu, Zhonghu, Li, Mingjin, Rosen, Orli, Zoog, Stephen J., W

Journal:

Year:

2018

Language:

english

File:

PDF, 1.40 MB

english, 2018

41

Long-term comparative effectiveness of pegvaliase versus standard of care comparators in adults with phenylketonuria

Zori, Roberto, Ahring, Kirsten, Burton, Barbara, Pastores, Gregory M., Rutsch, Frank, Jha, Ashok, Jurecki, Elaina, Rowell, Richard, Harding, Cary

Journal:

Molecular Genetics and Metabolism

Year:

2019

Language:

english

File:

PDF, 595 KB

english, 2019

42

The Mouse Mutation Sarcosinemia (sar) Maps to Chromosome 2 in a Region Homologous to Human 9q33–q34

Ana Lúcia Bueno Brunialti, Cary O. Harding, Jon A. Wolff, Jean-Louis Guénet

Journal:

Year:

1996

Language:

english

File:

PDF, 80 KB

english, 1996

43

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Melanie B Gillingham, William E Connor, Dietrich Matern, Piero Rinaldo, Terry Burlingame, Kaatje Meeuws, Cary O Harding

Journal:

Molecular Genetics and Metabolism

Year:

2003

Language:

english

File:

PDF, 248 KB

english, 2003

44

Autologous Gene and Cell Therapy Provides Safe and Long-Term Curative Therapy in A Large Pig Model of Hereditary Tyrosinemia Type 1

Hickey, Raymond D., Nicolas, Clara T., Allen, Kari, Mao, Shennen, Elgilani, Faysal, Glorioso, Jaime, Amiot, Bruce, VanLith, Caitlin, Guthman, Rebekah, Du, Zeji, Chen, Harvey, Harding, Cary O., Kaiser,

Journal:

Cell Transplantation

Year:

2018

Language:

english

File:

PDF, 1.09 MB

english, 2018

45

Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency

Sven W. Sauer, Jürgen G. Okun, Gert Fricker, Anne Mahringer, Ines Müller, Linda R. Crnic, Chris Mühlhausen, Georg F. Hoffmann, Friederike Hörster, Stephen I. Goodman, Cary O. Harding, David M. Koeller

Journal:

Journal of Neurochemistry

Year:

2006

Language:

english

File:

PDF, 432 KB

english, 2006

46

Correction of Murine PKU Following AAV-mediated Intramuscular Expression of a Complete Phenylalanine Hydroxylating System

Ding, Zhaobing, Harding, Cary O, Rebuffat, Alexandre, Elzaouk, Lina, Wolff, Jon A, Thöny, Beat

Journal:

Molecular Therapy

Year:

2008

Language:

english

File:

PDF, 306 KB

english, 2008

47

Therapeutic liver repopulation for phenylketonuria

Cary O. Harding, K. M. Gibson

Journal:

Journal of Inherited Metabolic Disease

Year:

2010

Language:

english

File:

PDF, 153 KB

english, 2010

48

Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency

Melanie B. Gillingham, Bradley Scott, Diane Elliott, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2006

Language:

english

File:

PDF, 237 KB

english, 2006

49

Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening

Merritt, J. Lawrence, Vedal, Sverre, Abdenur, Jose E., Au, Sylvia M., Barshop, Bruce A., Feuchtbaum, Lisa, Harding, Cary O., Hermerath, Cheryl, Lorey, Fred, Sesser, David E., Thompson, John D., Yu, Ar

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 742 KB

english, 2014

50

Normal Fatty Acid Concentrations in Young Children With Phenylketonuria

LaVoie, Stacey M., Harding, Cary O., Gillingham, Melanie B.

Journal:

Topics in Clinical Nutrition

Year:

2009

Language:

english

File:

PDF, 82 KB

english, 2009

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