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David Rosenblatt

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Li Fei; Watkins David; Rosenblatt David S
Vitamin B(12) and birth defects.
Lerner-Ellis Jordan P; Anastasio Natascia; Liu Junhui; Coelho David; Suormala Terttu; Stucki Martin; Loewy Amanda D; Gurd Scott; Grundberg Elin; Morel Chantal F; Watkins David; Baumgartner Matthias R; Pastinen Tomi; Rosenblatt David S; Fowler Brian
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Loewy Amanda D; Niles Kirsten M; Anastasio Natascia; Watkins David; Lavoie Josée; Lerner-Ellis Jordan P; Pastinen Tomi; Trasler Jacquetta M; Rosenblatt David S
Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.

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2009: Li Fei; Watkins David; Rosenblatt David S
Vitamin B(12) and birth defects.
Molecular genetics and metabolism 2009;98(1-2):166-72.
2009: Lerner-Ellis Jordan P; Anastasio Natascia; Liu Junhui; Coelho David; Suormala Terttu; Stucki Martin; Loewy Amanda D; Gurd Scott; Grundberg Elin; Morel Chantal F; Watkins David; Baumgartner Matthias R; Pastinen Tomi; Rosenblatt David S; Fowler Brian
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Human mutation 2009;30(7):1072-81.
2009: Loewy Amanda D; Niles Kirsten M; Anastasio Natascia; Watkins David; Lavoie Josée; Lerner-Ellis Jordan P; Pastinen Tomi; Trasler Jacquetta M; Rosenblatt David S
Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.
Molecular genetics and metabolism 2009;96(4):261-7.
2009: Miousse Isabelle R; Watkins David; Coelho David; Rupar Tony; Crombez Eric A; Vilain Eric; Bernstein Jonathan A; Cowan Tina; Lee-Messer Christopher; Enns Gregory M; Fowler Brian; Rosenblatt David S
Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
The Journal of pediatrics 2009;154(4):551-6.
2008: Yamani Lama; Gibbs Bernard F; Gilfix Brian M; Watkins David; Hosack Angela; Rosenblatt David S
Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism.
Molecular genetics and metabolism 2008;95(1-2):104-6.
2008: Coelho David; Suormala Terttu; Stucki Martin; Lerner-Ellis Jordan P; Rosenblatt David S; Newbold Robert F; Baumgartner Matthias R; Fowler Brian
Gene identification for the cblD defect of vitamin B12 metabolism.
The New England journal of medicine 2008;358(14):1454-64.
2007: Tsai Anne Chun-Hui; Morel Chantal F; Scharer Gunter; Yang Michael; Lerner-Ellis Jordan P; Rosenblatt David S; Thomas Janet A
Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance.
American journal of medical genetics. Part A 2007;143A(20):2430-4.
2007: Gradinger Abigail B; Bélair Caroline; Worgan Lisa C; Li Carter D; Lavallée Jocelyne; Roquis David; Watkins David; Rosenblatt David S
Atypical methylmalonic aciduria: frequency of mutations in the methylmalonyl CoA epimerase gene (MCEE).
Human mutation 2007;28(10):1045.
2007: Moras E; Hosack A; Watkins D; Rosenblatt D S
Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
Molecular genetics and metabolism 2007;90(2):140-7.
2006: Ernest Sheila; Carter Michelle; Shao Haifeng; Hosack Angela; Lerner Natalia; Colmenares Clemencia; Rosenblatt David S; Pao Yoh-Han; Ross M Elizabeth; Nadeau Joseph H
Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type mice.
Human molecular genetics 2006;15(23):3387-93.
2006: Morel Chantal F; Lerner-Ellis Jordan P; Rosenblatt David S
Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.
Molecular genetics and metabolism 2006;88(4):315-21.
2006: Dobson C Melissa; Gradinger Abigail; Longo Nicola; Wu Xuchu; Leclerc Daniel; Lerner-Ellis Jordan; Lemieux Melissa; Belair Caroline; Watkins David; Rosenblatt David S; Gravel Roy A
Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
Molecular genetics and metabolism 2006;88(4):327-33.
2006: Zhang Jun; Dobson C Melissa; Wu Xuchu; Lerner-Ellis Jordan; Rosenblatt David S; Gravel Roy A
Impact of cblB mutations on the function of ATP:cob(I)alamin adenosyltransferase in disorders of vitamin B12 metabolism.
Molecular genetics and metabolism 2006;87(4):315-22.
2006: Lerner-Ellis Jordan P; Gradinger Abigail B; Watkins David; Tirone Jamie C; Villeneuve Amélie; Dobson C Melissa; Montpetit Alexandre; Lepage Pierre; Gravel Roy A; Rosenblatt David S
Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria.
Molecular genetics and metabolism 2006;87(3):219-25.
2006: Lerner-Ellis Jordan P; Tirone Jamie C; Pawelek Peter D; Doré Carole; Atkinson Janet L; Watkins David; Morel Chantal F; Fujiwara T Mary; Moras Emily; Hosack Angela R; Dunbar Gail V; Antonicka Hana; Forgetta Vince; Dobson C Melissa; Leclerc Daniel; Gravel Roy A; Shoubridge Eric A; Coulton James W; Lepage Pierre; Rommens Johanna M; Morgan Kenneth; Rosenblatt David S
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Nature genetics 2006;38(1):93-100.
2006: Worgan Lisa C; Niles Kirsten; Tirone Jamie C; Hofmann Adam; Verner Andrei; Sammak Alya'a; Kucic Terrence; Lepage Pierre; Rosenblatt David S
Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.
Human mutation 2006;27(1):31-43.
2005: Morel Chantal F; Watkins David; Scott Patrick; Rinaldo Piero; Rosenblatt David S
Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
Molecular genetics and metabolism 2005;86(1-2):160-71.
2005: Morel Chantal F; Scott Patrick; Christensen Ernst; Rosenblatt David S; Rozen Rima
Prenatal diagnosis for severe methylenetetrahydrofolate reductase deficiency by linkage analysis and enzymatic assay.
Molecular genetics and metabolism 2005;85(2):115-20.
2005: Ernest Sheila; Hosack Angela; O'Brien William E; Rosenblatt David S; Nadeau Joseph H
Homocysteine levels in A/J and C57BL/6J mice: genetic, diet, gender, and parental effects.
Physiological genomics 2005;21(3):404-10.
2004: Lerner-Ellis Jordan P; Dobson C Melissa; Wai Timothy; Watkins David; Tirone Jamie C; Leclerc Daniel; Doré Carole; Lepage Pierre; Gravel Roy A; Rosenblatt David S
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism.
Human mutation 2004;24(6):509-16.
2003: Ernest Sheila; Carter Michelle; Hosack Angela; Rosenblatt David; Ross Elizabeth; Nadeau Joseph H
Nutrigenes, functional genomics and systems biology.
The Journal of nutrition 2003;133(12):4267-8.
2003: Hilton John F; Christensen Karen E; Watkins David; Raby Benjamin A; Renaud Yannick; de la Luna Susanna; Estivill Xavier; MacKenzie Robert E; Hudson Thomas J; Rosenblatt David S
The molecular basis of glutamate formiminotransferase deficiency.
Human mutation 2003;22(1):67-73.
2003: Sibani Sahar; Leclerc Daniel; Weisberg Ilan S; O'Ferrall Erin; Watkins David; Artigas Carmen; Rosenblatt David S; Rozen Rima
Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation.
Human mutation 2003;21(5):509-20.
2002: Dobson C Melissa; Wai Timothy; Leclerc Daniel; Kadir Hakan; Narang Monica; Lerner-Ellis Jordan P; Hudson Thomas J; Rosenblatt David S; Gravel Roy A
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria.
Human molecular genetics 2002;11(26):3361-9.
2002: Dobson C Melissa; Wai Timothy; Leclerc Daniel; Wilson Aaron; Wu Xuchu; Doré Carole; Hudson Thomas; Rosenblatt David S; Gravel Roy A
Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(24):15554-9.
2002: Watkins David; Ru Ming; Hwang Hye-Yeon; Kim Caroline D; Murray Angus; Philip Noah S; Kim William; Legakis Helen; Wai Timothy; Hilton John F; Ge Bing; Doré Carole; Hosack Angela; Wilson Aaron; Gravel Roy A; Shane Barry; Hudson Thomas J; Rosenblatt David S
Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.
American journal of human genetics 2002;71(1):143-53.
2002: Ernest Sheila; Christensen Benedicte; Gilfix Brian M; Mamer Orval A; Hosack Angela; Rodier Mitchell; Colmenares Clemencia; McGrath James; Bale Allen; Balling Rudi; Sankoff David; Rosenblatt David S; Nadeau Joseph H
Genetic and molecular control of folate-homocysteine metabolism in mutant mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(5):259-67.
2001: Mudd S H; Cerone R; Schiaffino M C; Fantasia A R; Minniti G; Caruso U; Lorini R; Watkins D; Matiaszuk N; Rosenblatt D S; Schwahn B; Rozen R; LeGros L; Kotb M; Capdevila A; Luka Z; Finkelstein J D; Tangerman A; Stabler S P; Allen R H; Wagner C
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.
Journal of inherited metabolic disease 2001;24(4):448-64.
2001: Rosenblatt D S
Methylenetetrahydrofolate reductase.
Clinical and investigative medicine. Médecine clinique et experimentale 2001;24(1):56-9.
2000: Watkins D; Matiaszuk N; Rosenblatt D S
Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH).
Journal of medical genetics 2000;37(7):510-3.
2000: Rosenblatt D S
The evolution of medicine--a geneticist's point of view.
Clinical and investigative medicine. Médecine clinique et experimentale 2000;23(1):59-61; discussion 62-3.
2000: Sibani S; Christensen B; O'Ferrall E; Saadi I; Hiou-Tim F; Rosenblatt D S; Rozen R
Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria.
Human mutation 2000;15(3):280-7.
1999: Wilson A; Leclerc D; Rosenblatt D S; Gravel R A
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
Human molecular genetics 1999;8(11):2009-16.
1999: Christensen B; Arbour L; Tran P; Leclerc D; Sabbaghian N; Platt R; Gilfix B M; Rosenblatt D S; Gravel R A; Forbes P; Rozen R
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.
American journal of medical genetics 1999;84(2):151-7.
1999: Rosenblatt D S; Whitehead V M
Cobalamin and folate deficiency: acquired and hereditary disorders in children.
Seminars in hematology 1999;36(1):19-34.
1998: Goyette P; Rosenblatt D; Rozen R
Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene.
Journal of inherited metabolic disease 1998;21(6):690-1.
1998: Wilson A; Leclerc D; Saberi F; Campeau E; Hwang H Y; Shane B; Phillips J A; Rosenblatt D S; Gravel R A
Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency.
American journal of human genetics 1998;63(2):409-14.
1998: Leclerc D; Wilson A; Dumas R; Gafuik C; Song D; Watkins D; Heng H H; Rommens J M; Scherer S W; Rosenblatt D S; Gravel R A
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(6):3059-64.
1998: Adjalla C E; Hosack A R; Gilfix B M; Lamothe E; Sun S; Chan A; Evans S; Matiaszuk N V; Rosenblatt D S
Seven novel mutations in mut methylmalonic aciduria.
Human mutation 1998;11(4):270-4.
1998: Adjalla C E; Hosack A R; Matiaszuk N V; Rosenblatt D S
A common mutation among blacks with mut- methylmalonic aciduria.
Human mutation 1998;Suppl 1():S248-50.
1997: Rosenblatt D S; Aspler A L; Shevell M I; Pletcher B A; Fenton W A; Seashore M R
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).
Journal of inherited metabolic disease 1997;20(4):528-38.
1997: Gilfix B M; Blank D W; Rosenblatt D S
Novel reductant for determination of total plasma homocysteine.
Clinical chemistry 1997;43(4):687-8.
1997: Christensen B; Frosst P; Lussier-Cacan S; Selhub J; Goyette P; Rosenblatt D S; Genest J; Rozen R
Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.
Arteriosclerosis, thrombosis, and vascular biology 1997;17(3):569-73.
1996: Leclerc D; Campeau E; Goyette P; Adjalla C E; Christensen B; Ross M; Eydoux P; Rosenblatt D S; Rozen R; Gravel R A
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Human molecular genetics 1996;5(12):1867-74.
1996: Goyette P; Christensen B; Rosenblatt D S; Rozen R
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.
American journal of human genetics 1996;59(6):1268-75.
1996: Rosenblatt D S; Ledley F D
[A molecular study of methylmalonic aciduria: structure-function correlations]
Bulletin de l'Académie nationale de médecine 1996;180(7):1553-63; discussion 1563-4.
1996: Rosenblatt D S; Fraser F C; Roy D J
Folic acid to prevent neural tube defects: time for food fortification.
Clinical and investigative medicine. Médecine clinique et experimentale 1996;19(3):202-3.
1995: Christensen B; Rosenblatt D S
Effects of folate deficiency on embryonic development.
Baillière's clinical haematology 1995;8(3):617-37.
1995: Paltiel O; Falutz J; Veilleux M; Rosenblatt D S; Gordon K
Clinical correlates of subnormal vitamin B12 levels in patients infected with the human immunodeficiency virus.
American journal of hematology 1995;49(4):318-22.
1995: Goyette P; Frosst P; Rosenblatt D S; Rozen R
Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.
American journal of human genetics 1995;56(5):1052-9.
1994: Chadefaux B; Cooper B A; Gilfix B M; Lue-Shing H; Carson W; Gavsie A; Rosenblatt D S
Homocysteine: relationship to serum cobalamin, serum folate, erythrocyte folate, and lobation of neutrophils.
Clinical and investigative medicine. Médecine clinique et experimentale 1994;17(6):540-50.
1994: Qureshi A A; Rosenblatt D S; Cooper B A
Inherited disorders of cobalamin metabolism.
Critical reviews in oncology/hematology 1994;17(2):133-51.
1994: Goyette P; Sumner J S; Milos R; Duncan A M; Rosenblatt D S; Matthews R G; Rozen R
Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.
Nature genetics 1994;7(4):551.
1994: Goyette P; Sumner J S; Milos R; Duncan A M; Rosenblatt D S; Matthews R G; Rozen R
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.
Nature genetics 1994;7(2):195-200.
1994: Qureshi A A; Crane A M; Matiaszuk N V; Rezvani I; Ledley F D; Rosenblatt D S
Cloning and expression of mutations demonstrating intragenic complementation in mut0 methylmalonic aciduria.
The Journal of clinical investigation 1994;93(4):1812-9.
1993: Haworth J C; Dilling L A; Surtees R A; Seargeant L E; Lue-Shing H; Cooper B A; Rosenblatt D S
Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers.
American journal of medical genetics 1993;45(5):572-6.
1993: Shevell M I; Matiaszuk N; Ledley F D; Rosenblatt D S
Varying neurological phenotypes among muto and mut- patients with methylmalonylCoA mutase deficiency.
American journal of medical genetics 1993;45(5):619-24.
1993: Rosenblatt D S; Lue-Shing H; Matiaszuk N; Low-Nang L; Arzoumanian A; Cooper B A
Thermolability of residual methylene-tetrahydrofolate reductase (MR) activity, methionine synthase activity and methyl-cobalamin levels in cultured fibroblasts from patients with MR deficiency.
Advances in experimental medicine and biology 1993;338():703-6.
1992: Shevell M I; Rosenblatt D S
The neurology of cobalamin.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1992;19(4):472-86.
1992: Rosenberg E E; Tannenbaum T N; Miller S D; Lamothe E M; Rosenblatt D S
Knowledge of nephrologists and patients about autosomal dominant polycystic kidney disease (ADPKD).
Clinical and investigative medicine. Médecine clinique et experimentale 1992;15(5):440-4.
1992: Garovic-Kocic V; Rosenblatt D S
Methionine auxotrophy in inborn errors of cobalamin metabolism.
Clinical and investigative medicine. Médecine clinique et experimentale 1992;15(4):395-400.
1992: Laframboise R; Cooper B A; Rosenblatt D S
Malabsorption of vitamin B12 from the intestine in a child with cblF disease: evidence for lysosomal-mediated absorption.
Blood 1992;80(1):291-2.
1992: Sillaots S L; Hall C A; Hurteloup V; Rosenblatt D S
Heterogeneity in cblG: differential retention of cobalamin on methionine synthase.
Biochemical medicine and metabolic biology 1992;47(3):242-9.
1992: Rosenblatt D S; Lue-Shing H; Arzoumanian A; Low-Nang L; Matiaszuk N
Methylenetetrahydrofolate reductase (MR) deficiency: thermolability of residual MR activity, methionine synthase activity, and methylcobalamin levels in cultured fibroblasts.
Biochemical medicine and metabolic biology 1992;47(3):221-5.
1992: Rosenblatt D S
Vitamin B12 (Cbl)-responsive disorders.
Journal of nutritional science and vitaminology 1992;Spec No():593-6.
1991: Liteplo R G; Hipwell S E; Rosenblatt D S; Sillaots S; Lue-Shing H
Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cells.
Journal of cellular physiology 1991;149(2):332-8.
1991: Raff M L; Crane A M; Jansen R; Ledley F D; Rosenblatt D S
Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.
The Journal of clinical investigation 1991;87(1):203-7.
1990: Whitehead V M; Rosenblatt D S; Vuchich M J; Shuster J J; Witte A; Beaulieu D
Accumulation of methotrexate and methotrexate polyglutamates in lymphoblasts at diagnosis of childhood acute lymphoblastic leukemia: a pilot prognostic factor analysis.
Blood 1990;76(1):44-9.
1990: McGill J J; Mettler G; Rosenblatt D S; Scriver C R
Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: paradigm of pitfalls in phenotypes.
American journal of medical genetics 1990;36(1):45-52.
1989: Watkins D; Rosenblatt D S
Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
American journal of medical genetics 1989;34(3):427-34.
1988: Watkins D; Rosenblatt D S
Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.
The Journal of clinical investigation 1988;81(6):1690-4.
1987: Rosenblatt D S; Cooper B A
Inherited disorders of vitamin B12 metabolism.
Blood reviews 1987;1(3):177-82.
1987: Joannon P; Whitehead V M; Rosenblatt D S; Vuchich M J; Beaulieu D
Methotrexate metabolism in mutant Chinese hamster ovary cells lacking dihydrofolate reductase.
Biochemical pharmacology 1987;36(7):1091-7.
1987: Rosenblatt D S; Hosack A; Matiaszuk N
Expression of transcobalamin II by amniocytes.
Prenatal diagnosis 1987;7(1):35-9.
1987: Whitehead V M; Rosenblatt D S; Vuchich M J; Beaulieu D
Methotrexate polyglutamate synthesis in lymphoblasts from children with acute lymphoblastic leukemia.
Developmental pharmacology and therapeutics 1987;10(6):443-8.
1986: Rosenblatt D S; Laframboise R; Pichette J; Langevin P; Cooper B A; Costa T
New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
Pediatrics 1986;78(1):51-4.
1985: Rosenblatt D S; Hosack A; Matiaszuk N V; Cooper B A; Laframboise R
Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism.
Science (New York, N.Y.) 1985;228(4705):1319-21.
1984: Rosenblatt D S; Cooper B A; Pottier A; Lue-Shing H; Matiaszuk N; Grauer K
Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
The Journal of clinical investigation 1984;74(6):2149-56.
1984: Schuh S; Rosenblatt D S; Cooper B A; Schroeder M L; Bishop A J; Seargeant L E; Haworth J C
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
The New England journal of medicine 1984;310(11):686-90.
1982: Rosenblatt D S; Whitehead V M; Matiaszuk N V; Pottier A; Vuchich M J; Beaulieu D
Differential effects of folinic acid and glycine, adenosine, and thymidine as rescue agents in methotrexate-treated human cells in relation to the accumulation of methotrexate polyglutamates.
Molecular pharmacology 1982;21(3):718-22.
1981: Rosenblatt D S; Whitehead V M; Vuchich M J; Pottier A; Matiaszuk N V; Beaulieu D
Inhibition of methotrexate polyglutamate accumulation in cultured human cells.
Molecular pharmacology 1981;19(1):87-91.
1980: Witte A; Whitehead V M; Rosenblatt D S; Vuchich M J
Synthesis of methotrexate polyglutamates by bone marrow cells from patients with leukemia and lymphoma.
Developmental pharmacology and therapeutics 1980;1(1):40-6.

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