K. Schappert

发表

HLA class I, II & III genes in confirmed late-onset Alzheimer’s disease

K. Morgan, A. Smith, D. Lehmann, 2001, Neurobiology of Aging.

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

J. Nadeau, K. Schappert, E. Ziętkiewicz, 2004, Mammalian Genome.

Isolation and characterization of Saccharomyces cerevisiae mutants resistant to T-2 toxin

K. Schappert, H. Koshinsky, G. Khachatourians, 1988, Current Genetics.

Further evidence for a synergistic association between APOE epsilon4 and BCHE-K in confirmed Alzheimer's disease.

H. Wiebusch, K. Schappert, J. Poirier, 1999, Human genetics.

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation.

R. Mcinnes, K. Schappert, R. Bascom, 1993, Human molecular genetics.

Genetic studies of the PRP11 izene of Saccharomyces cerevisiae

K. Schappert, J. Friesen, 1991, Molecular and General Genetics MGG.

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution.

D. Labuda, K. Schappert, A. Duncan, 1994, Genomics.

Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.

C. Obie, D. Valle, K. Schappert, 1995, American journal of human genetics.

Effects of T-2 toxin on induction of petite mutants and mitochondrial function in Saccharomyces cerevisiae

George G. Khachatourians, K. Schappert, G. Khachatourians, 2004, Current Genetics.

Molecular cloning and characterization of human endothelial nitric oxide synthase

K. Schappert, J. Wilcox, P. Marsden, 1992, FEBS letters.

Molecular cloning and characterization of the mouse UDP-N-acetylglucosamine : α-3-D-mannoside β-1,2-N-acetylglucosaminyltransferase I gene

J. Marth, K. Schappert, C. Kozak, 1992 .

Mutational analysis of Saccharomyces cerevisiae U4 small nuclear RNA identifies functionally important domains

K. Schappert, J. Friesen, Y. Xu, 1995, Molecular and cellular biology.

A mutation in the human ryanodine receptor gene associated with central core disease

M. Phillips, B. Britt, K. Schappert, 1993, Nature Genetics.

Human p68 kinase exhibits growth suppression in yeast and homology to the translational regulator GCN2.

K. Schappert, E. Meurs, J. Friesen, 1992, The EMBO journal.

Humanp68kinase exhibits growthsuppression inyeast andhomology tothetranslational regulator GCN2

K. Schappert, E. Meurs, 1992 .

Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene.

S. Scherer, H. Heng, L. Tsui, 1993, The Journal of biological chemistry.

Influence of the membrane on T-2 toxin toxicity in Saccharomyces spp

K. Schappert, G. Khachatourians, 1984, Applied and environmental microbiology.

Molecular cloning of the cDNA and chromosomal localization of the gene for a putative seven-transmembrane segment (7-TMS) receptor isolated from human spleen.

Allen D. Delaney, A. Delaney, K. Schappert, 1993, Genomics.

Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease

J. Rommens, M. Hayden, H. McDonald, 1993, Nature.

Genomic organization and complete sequence of the human gene encoding the β-subunit of the cGMP phosphodiesterase and its localisation to 4p16.3

D. Kowbel, C. Collins, M. Hayden, 1991 .

The deduced sequence of the transcription factor TFIIIA from Saccharomyces cerevisiae reveals extensive divergence from Xenopus TFIIIA.

K. Schappert, J. Archambault, J. Friesen, 1992, The Journal of biological chemistry.

Further evidence for a synergistic association between APOEɛ4 and BCHE-K in confirmed Alzheimer’s disease

H. Wiebusch, K. Schappert, J. Poirier, 1999, Human Genetics.

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13.

H. Heng, L. Tsui, K. Schappert, 1993, Genomics.

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency.

K. Schappert, K. Gibson, M. Robert, 1993, The Journal of biological chemistry.

A suppressor of an RNA polymerase II mutation of Saccharomyces cerevisiae encodes a subunit common to RNA polymerases I, II, and III

K. Schappert, J. Archambault, J. Friesen, 1990, Molecular and cellular biology.

Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

M. Corey, L. Tsui, J. Zieleński, 1995, Human mutation.

Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex.

Stephen H. Bell, J. Rommens, G. Fishman, 1994, Human molecular genetics.

Cloning and mapping of the alpha-adducin gene close to D4S95 and assessment of its relationship to Huntington disease.

K. Schappert, D. Ginzinger, S. Andrew, 1992, Human molecular genetics.

The genomic organization of a novel regulatory myosin light chain gene (MYL5) that maps to chromosome 4p16.3 and shows different patterns of expression between primates.

C. Collins, M. Hayden, K. Schappert, 1992, Human molecular genetics.

Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3.

D. Kowbel, C. Collins, M. Hayden, 1991, Nucleic acids research.

Pharmacogenetics of Psychotropic Drugs: Apolipoprotein E as a marker in the treatment of Alzheimer's disease

K. Schappert, J. Poirier, P. Sevigny, 2002 .