Viktor Kozich

Viktor Kozich

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Viktor Kozich

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Jan Kraus PhD., Professor of Pediatrics at the University of Colorado Anschutz Medical Campus, Aurora, CO, USA (b London, UK, June 5, 1942; q 1965 Faculty of Science Prague, d July 4, 2019, CO, USA).

J Inherit Metab Dis 2020 Mar;43(2):379-380

Institute of Inherited Metabolic Disorders, Charles University, Prague, Czech Republic.

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http://dx.doi.org/10.1002/jimd.12169DOI Listing
March 2020

Epidemiology of rare diseases detected by newborn screening in the Czech Republic.

Cent Eur J Public Health 2019 Jun;27(2):153-159

Department of Children and Adolescents, Third Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, Prague, Czech Republic.

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http://dx.doi.org/10.21101/cejph.a5441DOI Listing
June 2019

Comprehensive analysis of how experimental parameters affect HS measurements by the monobromobimane method.

Free Radic Biol Med 2019 05 7;136:146-158. Epub 2019 Apr 7.

National Institute of Oncology, Department of Molecular Immunology and Toxicology, Ráth György Utca 7-9, Budapest, Hungary; Department of Medicine, Faculty of Medicine, University of Debrecen, 4012, Debrecen, Hungary. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08915849193030
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http://dx.doi.org/10.1016/j.freeradbiomed.2019.04.006DOI Listing
May 2019

Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry.

J Inherit Metab Dis 2019 03 17;42(2):333-352. Epub 2019 Feb 17.

Inherited Metabolic Diseases Clinic, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado.

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http://dx.doi.org/10.1002/jimd.12041DOI Listing
March 2019

Metabolism of sulfur compounds in homocystinurias.

Br J Pharmacol 2019 02 25;176(4):594-606. Epub 2018 Nov 25.

Department of Molecular Immunology and Toxicology, National Institute of Oncology, Budapest, Hungary.

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http://dx.doi.org/10.1111/bph.14523DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346072PMC
February 2019

Neonatal screening in the Czech Republic: increased prevalence of selected diseases in low birthweight neonates.

Eur J Pediatr 2018 Nov 22;177(11):1697-1704. Epub 2018 Aug 22.

Department of Children and Adolescents, Third Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, Srobarova 1150/50, 100 34, Prague 10, Czech Republic.

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http://dx.doi.org/10.1007/s00431-018-3230-yDOI Listing
November 2018

Potential Pharmacological Chaperones for Cystathionine Beta-Synthase-Deficient Homocystinuria.

Handb Exp Pharmacol 2018 ;245:345-383

Department of Pediatrics, School of Medicine, University of Colorado, Aurora, CO, USA.

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http://dx.doi.org/10.1007/164_2017_72DOI Listing
September 2018

Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria.

Mol Ther 2018 03 19;26(3):834-844. Epub 2017 Dec 19.

Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S15250016173061
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http://dx.doi.org/10.1016/j.ymthe.2017.12.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910661PMC
March 2018

Biogenesis of Hydrogen Sulfide and Thioethers by Cystathionine Beta-Synthase.

Antioxid Redox Signal 2018 02 11;28(4):311-323. Epub 2017 Oct 11.

1 Department of Pediatrics, University of Colorado , School of Medicine, Aurora, Colorado.

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http://dx.doi.org/10.1089/ars.2017.7009DOI Listing
February 2018

Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine homocystinuria.

FASEB J 2017 12 16;31(12):5495-5506. Epub 2017 Aug 16.

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA;

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http://dx.doi.org/10.1096/fj.201700565RDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690381PMC
December 2017

Thioethers as markers of hydrogen sulfide production in homocystinurias.

Biochimie 2016 Jul 11;126:14-20. Epub 2016 Jan 11.

Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.

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http://dx.doi.org/10.1016/j.biochi.2016.01.001DOI Listing
July 2016

Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.

Hum Mutat 2016 May 18;37(5):427-38. Epub 2016 Mar 18.

Division of Metabolism and Children's Research Center, University Children's Hospital, Zürich, CH-8032, Switzerland.

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http://dx.doi.org/10.1002/humu.22970DOI Listing
May 2016

Genetic Variation in Renal Expression of Folate Receptor 1 (Folr1) Gene Predisposes Spontaneously Hypertensive Rats to Metabolic Syndrome.

Hypertension 2016 Feb 14;67(2):335-41. Epub 2015 Dec 14.

From the Department of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic (M.P., V.Z., V.L., P.M., J.Š., M.Š.); Institute of Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic (V.K., J.K., J.Š.); Center of Experimental Medicine, Department of Metabolism and Diabetes, Institute for Clinical and Experimental Medicine, Prague, Czech Republic (V.Š., J.T., L.K.); and Department of Laboratory Medicine, University of California, San Francisco (T.K., J.W., T.W.K.).

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http://dx.doi.org/10.1161/HYPERTENSIONAHA.115.06158DOI Listing
February 2016

Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.

J Inherit Metab Dis 2015 Nov 12;38(6):1007-19. Epub 2015 Mar 12.

Laboratory Clinical Biochemistry and Metabolism, Center for Pediatrics and Adolescent Medicine University Hospital, Freiburg, Freiburg, Germany.

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http://link.springer.com/10.1007/s10545-015-9830-z
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http://dx.doi.org/10.1007/s10545-015-9830-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626539PMC
November 2015

Metabolic syndrome, alcohol consumption and genetic factors are associated with serum uric acid concentration.

PLoS One 2014 14;9(5):e97646. Epub 2014 May 14.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0097646PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020828PMC
June 2015

Chaperone therapy for homocystinuria: the rescue of CBS mutations by heme arginate.

J Inherit Metab Dis 2015 Mar 21;38(2):287-94. Epub 2014 Oct 21.

Institute of Inherited Metabolic Disorders, Charles University in Prague-First Faculty of Medicine and General University Hospital in Prague, Ke Karlovu 2, 128 08, Praha 2, Czech Republic.

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http://dx.doi.org/10.1007/s10545-014-9781-9DOI Listing
March 2015

CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.

Hum Genet 2015 Mar 28;134(3):291-303. Epub 2014 Dec 28.

Human Molecular Genetics Group, Institute of Molecular and Cell Biology, University of Tartu, Riia St. 23, 51010, Tartu, Estonia.

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http://dx.doi.org/10.1007/s00439-014-1521-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318987PMC
March 2015

Simultaneous determination of cystathionine, total homocysteine, and methionine in dried blood spots by liquid chromatography/tandem mass spectrometry and its utility for the management of patients with homocystinuria.

Clin Chim Acta 2014 Nov 31;437:211-7. Epub 2014 Jul 31.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00098981140031
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http://dx.doi.org/10.1016/j.cca.2014.07.028DOI Listing
November 2014

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).

Eur J Hum Genet 2014 Feb 14;22(2):160-70. Epub 2013 Aug 14.

National Centre for Medical Genetics, School of Medicine & Medical Sciences, University College Dublin, Our Lady's Children's Hospital, Dublin, Ireland.

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http://dx.doi.org/10.1038/ejhg.2013.125DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895644PMC
February 2014

Biochemical properties of nematode O-acetylserine(thiol)lyase paralogs imply their distinct roles in hydrogen sulfide homeostasis.

Biochim Biophys Acta 2013 Dec 4;1834(12):2691-701. Epub 2013 Oct 4.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Ke Karlovu 2, Prague 2, 128 08, Czech Republic.

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http://dx.doi.org/10.1016/j.bbapap.2013.09.020DOI Listing
December 2013

Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.

Mol Genet Metab 2012 Nov 23;107(3):611-3. Epub 2012 Aug 23.

First Faculty of Medicine, Institute of Inherited Metabolic Disorders, Charles University in Prague and General University Hospital in Prague, Czech Republic.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921200314
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http://dx.doi.org/10.1016/j.ymgme.2012.08.014DOI Listing
November 2012

Rare allelic variants determine folate status in an unsupplemented European population.

J Nutr 2012 Aug 13;142(8):1403-9. Epub 2012 Jun 13.

Department of Medical Informatics, Institute of Computer Science of the Academy of Sciences of the Czech Republic, Prague, Czech Republic.

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http://dx.doi.org/10.3945/jn.112.160549DOI Listing
August 2012

Cystathionine beta-synthase mutants exhibit changes in protein unfolding: conformational analysis of misfolded variants in crude cell extracts.

J Inherit Metab Dis 2012 May 9;35(3):469-77. Epub 2011 Nov 9.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Ke Karlovu 2, 128 08, Prague 2, Czech Republic.

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http://dx.doi.org/10.1007/s10545-011-9407-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319881PMC
May 2012

Novel structural arrangement of nematode cystathionine β-synthases: characterization of Caenorhabditis elegans CBS-1.

Biochem J 2012 Apr;443(2):535-47

Institute of Inherited Metabolic Disorders, Charles University in Prague, First Faculty of Medicine and General University Hospital, Praha, Czech Republic.

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http://biochemj.org/lookup/doi/10.1042/BJ20111478
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http://dx.doi.org/10.1042/BJ20111478DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316156PMC
April 2012

Cysteine and obesity.

Obesity (Silver Spring) 2012 Mar 5;20(3):473-81. Epub 2011 May 5.

Department of Pharmacology, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/oby.2011.93DOI Listing
March 2012

Cysteine and obesity: consistency of the evidence across epidemiologic, animal and cellular studies.

Curr Opin Clin Nutr Metab Care 2012 Jan;15(1):49-57

Department of Pharmacology, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1097/MCO.0b013e32834d199fDOI Listing
January 2012

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.

Authors:
David M S McHugh Cynthia A Cameron Jose E Abdenur Mahera Abdulrahman Ona Adair Shahira Ahmed Al Nuaimi Henrik Åhlman Jennifer J Allen Italo Antonozzi Shaina Archer Sylvia Au Christiane Auray-Blais Mei Baker Fiona Bamforth Kinga Beckmann Gessi Bentz Pino Stanton L Berberich Robert Binard François Boemer Jim Bonham Nancy N Breen Sandra C Bryant Michele Caggana S Graham Caldwell Marta Camilot Carlene Campbell Claudia Carducci Sandra C Bryant Michele Caggana S Graham Caldwell Marta Camilot Carlene Campbell Claudia Carducci Rohit Cariappa Clover Carlisle Ubaldo Caruso Michela Cassanello Ane Miren Castilla Daisy E Castiñeiras Ramos Pranesh Chakraborty Ram Chandrasekar Alfredo Chardon Ramos David Cheillan Yin-Hsiu Chien Thomas A Childs Petr Chrastina Yuri Cleverthon Sica Jose Angel Cocho de Juan Maria Elena Colandre Veronica Cornejo Espinoza Gaetano Corso Robert Currier Denis Cyr Noemi Czuczy Oceania D'Apolito Tim Davis Monique G de Sain-Van der Velden Carmen Delgado Pecellin Iole Maria Di Gangi Cristina Maria Di Stefano Yannis Dotsikas Melanie Downing Stephen M Downs Bonifacio Dy Mark Dymerski Inmaculada Rueda Bert Elvers Roger Eaton Barbara M Eckerd Fatma El Mougy Sarah Eroh Mercedes Espada Catherine Evans Sandy Fawbush Kristel F Fijolek Lawrence Fisher Leifur Franzson Dianne M Frazier Luciana R C Garcia Maria Sierra García-Valdecasas Bermejo Dimitar Gavrilov Rosemarie Gerace Giuseppe Giordano Yolanda González Irazabal Lawrence C Greed Robert Grier Elyse Grycki Xuefan Gu Fizza Gulamali-Majid Arthur F Hagar Lianshu Han W Harry Hannon Christa Haslip Fayza Abdelhamid Hassan Miao He Amy Hietala Leslie Himstedt Gary L Hoffman William Hoffman Philis Hoggatt Patrick V Hopkins David M Hougaard Kerie Hughes Patricia R Hunt Wuh-Liang Hwu June Hynes Isabel Ibarra-González Cindy A Ingham Maria Ivanova Ward B Jacox Catharine John John P Johnson Jón J Jónsson Eszter Karg David Kasper Brenda Klopper Dimitris Katakouzinos Issam Khneisser Detlef Knoll Hirinori Kobayashi Ronald Koneski Viktor Kozich Rasoul Kouapei Dirk Kohlmueller Ivo Kremensky Giancarlo la Marca Marcia Lavochkin Soo-Youn Lee Denis C Lehotay Aida Lemes Joyce Lepage Barbara Lesko Barry Lewis Carol Lim Sharon Linard Martin Lindner Michele A Lloyd-Puryear Fred Lorey Yannis L Loukas Julie Luedtke Neil Maffitt J Fergall Magee Adrienne Manning Shawn Manos Sandrine Marie Sônia Marchezi Hadachi Gregg Marquardt Stephen J Martin Dietrich Matern Stephanie K Mayfield Gibson Philip Mayne Tonya D McCallister Mark McCann Julie McClure James J McGill Christine D McKeever Barbara McNeilly Mark A Morrissey Paraskevi Moutsatsou Eleanor A Mulcahy Dimitris Nikoloudis Bent Norgaard-Pedersen Devin Oglesbee Mariusz Oltarzewski Daniela Ombrone Jelili Ojodu Vagelis Papakonstantinou Sherly Pardo Reoyo Hyung-Doo Park Marzia Pasquali Elisabetta Pasquini Pallavi Patel Kenneth A Pass Colleen Peterson Rolf D Pettersen James J Pitt Sherry Poh Arnold Pollak Cory Porter Philip A Poston Ricky W Price Cecilia Queijo Jonessy Quesada Edward Randell Enzo Ranieri Kimiyo Raymond John E Reddic Alejandra Reuben Charla Ricciardi Piero Rinaldo Jeff D Rivera Alicia Roberts Hugo Rocha Geraldine Roche Cheryl Rochman Greenberg José María Egea Mellado María Jesús Juan-Fita Consuelo Ruiz Margherita Ruoppolo S Lane Rutledge Euijung Ryu Christine Saban Inderneel Sahai Maria Isabel Salazar García-Blanco Pedro Santiago-Borrero Andrea Schenone Roland Schoos Barb Schweitzer Patricia Scott Margretta R Seashore Mary A Seeterlin David E Sesser Darrin W Sevier Scott M Shone Graham Sinclair Victor A Skrinska Eleanor L Stanley Erin T Strovel April L Studinski Jones Sherlykutty Sunny Zoltan Takats Tijen Tanyalcin Francesca Teofoli J Robert Thompson Kathy Tomashitis Mouseline Torquado Domingos Jasmin Torres Rosario Torres Silvia Tortorelli Sandor Turi Kimberley Turner Nick Tzanakos Alf G Valiente Hillary Vallance Marcela Vela-Amieva Laura Vilarinho Ulrika von Döbeln Marie-Francoise Vincent B Chris Vorster Michael S Watson Dianne Webster Sheila Weiss Bridget Wilcken Veronica Wiley Sharon K Williams Sharon A Willis Michael Woontner Katherine Wright Raquel Yahyaoui Seiji Yamaguchi Melissa Yssel Wendy M Zakowicz

Genet Med 2011 Mar;13(3):230-54

Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1097/GIM.0b013e31820d5e67DOI Listing
March 2011

Restoring assembly and activity of cystathionine β-synthase mutants by ligands and chemical chaperones.

J Inherit Metab Dis 2011 Feb 20;34(1):39-48. Epub 2010 May 20.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Praha, Czech Republic.

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http://doi.wiley.com/10.1007/s10545-010-9087-5
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http://dx.doi.org/10.1007/s10545-010-9087-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026675PMC
February 2011

Vascular presentation of cystathionine beta-synthase deficiency in adulthood.

J Inherit Metab Dis 2011 Feb 22;34(1):33-7. Epub 2010 Jun 22.

Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University in Prague, Praha, Czech Republic.

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http://dx.doi.org/10.1007/s10545-010-9146-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026685PMC
February 2011

Determination of cystathionine beta-synthase activity in human plasma by LC-MS/MS: potential use in diagnosis of CBS deficiency.

J Inherit Metab Dis 2011 Feb 7;34(1):49-55. Epub 2010 Sep 7.

Institute of Inherited Metabolic Disorders--1st Faculty of Medicine, Charles University in Prague, Praha, Czech Republic.

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http://dx.doi.org/10.1007/s10545-010-9178-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026677PMC
February 2011

Cross-talk between the catalytic core and the regulatory domain in cystathionine β-synthase: study by differential covalent labeling and computational modeling.

Biochemistry 2010 Dec 17;49(49):10526-34. Epub 2010 Nov 17.

Institute of Inherited Metabolic Disorders, First Medical Faculty, Charles University in Prague and General University Hospital in Prague, Ke Karlovu 2, Prague 2, 128 00 Czech Republic.

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http://pubs.acs.org/doi/abs/10.1021/bi101384m
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http://dx.doi.org/10.1021/bi101384mDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146298PMC
December 2010

The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations.

J Inherit Metab Dis 2010 Aug 20;33(4):387-96. Epub 2010 May 20.

Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Ke Karlovu 2, 128 08, Prague 2, Czech Republic.

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http://link.springer.com/10.1007/s10545-010-9093-7
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http://dx.doi.org/10.1007/s10545-010-9093-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2903693PMC
August 2010

Cystathionine beta-synthase mutations: effect of mutation topology on folding and activity.

Hum Mutat 2010 Jul;31(7):809-19

First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Institute of Inherited Metabolic Disorders, Prague, Czech Republic.

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http://dx.doi.org/10.1002/humu.21273DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966864PMC
July 2010

Determination of S-Adenosylmethionine and S-Adenosylhomocysteine by LC-MS/MS and evaluation of their stability in mice tissues.

J Chromatogr B Analyt Technol Biomed Life Sci 2009 Jul 28;877(22):2061-6. Epub 2009 May 28.

Institute of Inherited Metabolic Disorders, Charles University in Prague - 1st Faculty of Medicine, Prague, Czech Republic.

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http://dx.doi.org/10.1016/j.jchromb.2009.05.039DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724122PMC
July 2009

Birth prevalence of homocystinuria in Central Europe: frequency and pathogenicity of mutation c.1105C>T (p.R369C) in the cystathionine beta-synthase gene.

J Pediatr 2009 Mar 31;154(3):431-7. Epub 2008 Oct 31.

Institute of Inherited Metabolic Disorders, Charles University in Prague-1st Faculty of Medicine, Prague, Czech Republic.

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http://dx.doi.org/10.1016/j.jpeds.2008.09.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2653617PMC
March 2009

Cystathionine beta-synthase p.S466L mutation causes hyperhomocysteinemia in mice.

Hum Mutat 2008 Aug;29(8):1048-54

Division of Population Science, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.

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http://doi.wiley.com/10.1002/humu.20773
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http://dx.doi.org/10.1002/humu.20773DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630375PMC
August 2008

Chemical chaperone rescue of mutant human cystathionine beta-synthase.

Mol Genet Metab 2007 Aug 30;91(4):335-42. Epub 2007 May 30.

Division of Population Science, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920700136
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http://dx.doi.org/10.1016/j.ymgme.2007.04.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040066PMC
August 2007

Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1.

BMC Med Genet 2007 Jul 23;8:47. Epub 2007 Jul 23.

Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1186/1471-2350-8-47DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1947951PMC
July 2007

Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population?

Eur J Hum Genet 2005 Jan;13(1):86-95

Institute of Inherited Metabolic Disorders, Charles University, 1st Faculty of Medicine, Prague, Czech Republic.

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http://dx.doi.org/10.1038/sj.ejhg.5201282DOI Listing
January 2005

Identification and functional analysis of two novel mutations in the CBS gene in Polish patients with homocystinuria.

Hum Mutat 2004 Jun;23(6):631

Institute of Inherited Metabolic Diseases, Charles University - First Faculty of Medicine, Prague, Czech Republic.

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http://dx.doi.org/10.1002/humu.9249DOI Listing
June 2004

Effect of folic acid on fenofibrate-induced elevation of homocysteine and cysteine.

Am Heart J 2003 Jul;146(1):110

Third Department of Internal Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.

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http://dx.doi.org/10.1016/S0002-8703(03)00122-4DOI Listing
July 2003

Essential hypertension in adolescents: association with insulin resistance and with metabolism of homocysteine and vitamins.

Am J Hypertens 2002 Oct;15(10 Pt 1):857-64

Institute of Inherited Metabolic Disease, Charles University, 1st Faculty of Medicine, Prague, Czech Republic.

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http://dx.doi.org/10.1016/s0895-7061(02)02984-9DOI Listing
October 2002