Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

270 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity.
Weisberg I, Tran P, Christensen B, Sibani S, Rozen R. Weisberg I, et al. Among authors: rozen r. Mol Genet Metab. 1998 Jul;64(3):169-72. doi: 10.1006/mgme.1998.2714. Mol Genet Metab. 1998. PMID: 9719624
Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.
Rozen R, De Braekeleer M, Daigneault J, Ferreira-Rajabi L, Gerdes M, Lamoureux L, Aubin G, Simard F, Fujiwara TM, Morgan K. Rozen R, et al. Am J Med Genet. 1992 Feb 1;42(3):360-4. doi: 10.1002/ajmg.1320420322. Am J Med Genet. 1992. PMID: 1536179
Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.
Slipetz DM, Aprille JR, Goodyer PR, Rozen R. Slipetz DM, et al. Among authors: rozen r. Am J Hum Genet. 1991 Mar;48(3):502-10. Am J Hum Genet. 1991. PMID: 1847791 Free PMC article.
Deficient synthesis of MTHFD, a trifunctional folate-dependent enzyme, in the CHO Ade E mutant.
Mascisch A, Rozen R. Mascisch A, et al. Among authors: rozen r. Somat Cell Mol Genet. 1991 Jul;17(4):391-8. doi: 10.1007/BF01233064. Somat Cell Mol Genet. 1991. PMID: 1887335
Congenital deficiency of a 20-kDa subunit of mitochondrial complex I in fibroblasts.
Slipetz DM, Goodyer PR, Rozen R. Slipetz DM, et al. Among authors: rozen r. Am J Hum Genet. 1991 Jun;48(6):1121-6. Am J Hum Genet. 1991. PMID: 1903590 Free PMC article.
A pseudogene on the X chromosome for the human trifunctional enzyme MTHFD (methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase).
Italiano C, John SW, Hum DW, MacKenzie RE, Rozen R. Italiano C, et al. Among authors: rozen r. Genomics. 1991 Aug;10(4):1073-4. doi: 10.1016/0888-7543(91)90201-o. Genomics. 1991. PMID: 1916813
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutations.
John SW, Rozen R, Scriver CR, Laframboise R, Laberge C. John SW, et al. Among authors: rozen r. Am J Hum Genet. 1990 May;46(5):970-4. Am J Hum Genet. 1990. PMID: 1971147 Free PMC article.
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families.
Rozen R, Schwartz RH, Hilman BC, Stanislovitis P, Horn GT, Klinger K, Daigneault J, De Braekeleer M, Kerem B, Tsui L, et al. Rozen R, et al. Am J Hum Genet. 1990 Oct;47(4):606-10. Am J Hum Genet. 1990. PMID: 2220803 Free PMC article.
Purification and characterization of methylenetetrahydrofolate reductase from human cadaver liver.
Zhou J, Kang SS, Wong PW, Fournier B, Rozen R. Zhou J, et al. Among authors: rozen r. Biochem Med Metab Biol. 1990 Jun;43(3):234-42. doi: 10.1016/0885-4505(90)90029-z. Biochem Med Metab Biol. 1990. PMID: 2383427
Novel PKU mutation on haplotype 2 in French-Canadians.
John SW, Rozen R, Laframboise R, Laberge C, Scriver CR. John SW, et al. Among authors: rozen r. Am J Hum Genet. 1989 Dec;45(6):905-9. Am J Hum Genet. 1989. PMID: 2574002 Free PMC article.
270 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback