Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.
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[1] S. Humphries,et al. Gene probes in diagnosis of familial hypercholesterolemia. , 1989, Arteriosclerosis.
[2] T. Holm,et al. A locus on chromosome 11p with multiple restriction site polymorphisms. , 1984, American journal of human genetics.
[3] H. Hobbs,et al. Multiple crm- mutations in familial hypercholesterolemia. Evidence for 13 alleles, including four deletions. , 1988, The Journal of clinical investigation.
[4] G. Coetzee,et al. Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners. , 1989, The Journal of clinical investigation.
[5] T. Ohta,et al. Linkage disequilibrium at steady state determined by random genetic drift and recurrent mutation. , 1969, Genetics.
[6] N. Zöllner,et al. Use of fibroblast culture to diagnose and genotype familial hypercholesterolaemia. , 1982, Annals of nutrition & metabolism.
[7] D. Russell,et al. The Lebanese allele at the low density lipoprotein receptor locus. Nonsense mutation produces truncated receptor that is retained in endoplasmic reticulum. , 1987, The Journal of biological chemistry.
[8] D. Botstein,et al. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.
[9] S. Grundy,et al. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[10] A. Kessling,et al. Identification of a second “French Canadian” LDL receptor gene deletion and development of a rapid method to detect both deletions , 1989, Clinical Genetics.
[11] C. Sing,et al. Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster. , 1991, American journal of human genetics.
[12] D. Russell,et al. The human LDL receptor: A cysteine-rich protein with multiple Alu sequences in its mRNA , 1984, Cell.
[13] D. Russell,et al. Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia , 1987, Cell.
[14] AvaII polymorphism in the human LDL receptor gene , 1987 .
[15] H. Grüneberg,et al. Introduction to quantitative genetics , 1960 .
[16] P. Brink,et al. A DNA polymorphism in the human low-density lipoprotein receptor gene. , 1986, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.
[17] A. Chakravarti,et al. Polymorphic DNA haplotypes at the LDL receptor locus. , 1989, American journal of human genetics.
[18] S. Humphries,et al. A COMMON DNA POLYMORPHISM OF THE LOW-DENSITY LIPOPROTEIN (LDL) RECEPTOR GENE AND ITS USE IN DIAGNOSIS , 1985, The Lancet.
[19] M. Greenwood. An Introduction to Medical Statistics , 1932, Nature.
[20] T. Südhof,et al. The LDL receptor gene: a mosaic of exons shared with different proteins. , 1985, Science.
[21] P. Kovanen,et al. Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype. , 1989, The Journal of clinical investigation.
[22] TaqI polymorphism in the human LDL receptor gene. , 1987, Nucleic acids research.
[23] M. Kotze,et al. Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor gene. , 1989, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.
[24] M. Kotze,et al. Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus. , 1989, Journal of medical genetics.
[25] L. Jorde,et al. Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. , 1986, American journal of human genetics.
[26] P. Linsley,et al. Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[27] M. Kotze,et al. The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia. , 1989, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.
[28] H. Hobbs,et al. Deletion in the gene for the low-density-lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia. , 1987, The New England journal of medicine.
[29] T. Südhof,et al. Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains. , 1985, Science.
[30] H. Hobbs,et al. Human LDL receptor gene: two ApaLI RFLPs. , 1987, Nucleic acids research.
[31] K. Buetow,et al. A strategy for using multiple linked markers for genetic counseling. , 1985, American journal of human genetics.
[32] G. Dahlberg,et al. Genetics of human populations. , 1948, Advances in genetics.
[33] R. Hudson,et al. Statistical properties of the number of recombination events in the history of a sample of DNA sequences. , 1985, Genetics.
[34] J. Sved. Linkage disequilibrium and homozygosity of chromosome segments in finite populations. , 1971, Theoretical population biology.
[35] N. Mantel. The detection of disease clustering and a generalized regression approach. , 1967, Cancer research.
[36] R. White. Mapping human chromosomes. , 1984, Harvey lectures.
[37] S. Antonarakis,et al. Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[38] Shirley A. Miller,et al. A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.
[39] R. Williamson,et al. Unequal crossing-over between two alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. A possible mechanism for the defect in a patient with familial hypercholesterolaemia. , 1987, European journal of biochemistry.
[40] R. Lewontin. The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. , 1964, Genetics.
[41] V. Gudnason,et al. A study of familial hypercholesterolaemia in Iceland using RFLPs. , 1989, Journal of medical genetics.
[42] H. Schuster,et al. Allele-specific and asymmetric polymerase chain reaction amplification in combination: a one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100. , 1992, Analytical biochemistry.
[43] H. Hobbs,et al. Human LDL receptor gene: HincII polymorphism detected by gene amplification. , 1988, Nucleic acids research.
[44] M. Permutt,et al. Evidence for increased recombination near the human insulin gene: implication for disease association studies. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[45] C. Sing,et al. Genetic structure and the search for genotype-phenotype relationships: an example from disequilibrium in the Apo B gene region. , 1991, Genetics.
[46] Maritha J. Kotze,et al. A RFLP associated with the low-density lipoprotein receptor gene (LDLR) , 1987, Nucleic Acids Res..
[47] H. Hobbs,et al. Deletion of exon encoding cysteine-rich repeat of low density lipoprotein receptor alters its binding specificity in a subject with familial hypercholesterolemia. , 1986, The Journal of biological chemistry.