Human genes containing polymorphic trinucleotide repeats

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  C. L. Warner,et al.  Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy , 1992, Nature Genetics.

[3]  J. Sutcliffe,et al.  DNA methylation represses FMR-1 transcription in fragile X syndrome. , 1992, Human molecular genetics.

[4]  W. Reardon,et al.  Anticipation in myotonic dystrophy: new light on an old problem. , 1992, American journal of human genetics.

[5]  K. Friend,et al.  Evidence of founder chromosomes in fragile X syndrome , 1992, Nature Genetics.

[6]  J. Mandel,et al.  Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy. , 1992, Human molecular genetics.

[7]  W. Reardon,et al.  Unstable DNA sequence in myotonic dystrophy , 1992, The Lancet.

[8]  T. Ashizawa,et al.  An unstable triplet repeat in a gene related to myotonic muscular dystrophy. , 1992, Science.

[9]  C. Amemiya,et al.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. , 1992, Science.

[10]  David E. Housman,et al.  Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member , 1992, Cell.

[11]  J. Sutcliffe,et al.  Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox , 1991, Cell.

[12]  N. Galjart,et al.  A mutation in a mild form of galactosialidosis impairs dimerization of the protective protein and renders it unstable. , 1991, The EMBO journal.

[13]  Ben A. Oostra,et al.  Absence of expression of the FMR-1 gene in fragile X syndrome , 1991, Cell.

[14]  D. S. Rath,et al.  Trinucleotide repeat polymorphism at the human transcription factor IID gene. , 1991, Nucleic acids research.

[15]  K. Fischbeck,et al.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.

[16]  D. Shaw,et al.  Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. , 1991, American journal of human genetics.

[17]  R I Richards,et al.  Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n , 1991, Science.

[18]  N. Galjart,et al.  The gene encoding human protective protein (PPGB) is on chromosome 20. , 1991, Genomics.

[19]  J. Sutcliffe,et al.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome , 1991, Cell.

[20]  D. Schlessinger,et al.  Fragile X genotype characterized by an unstable region of DNA , 1991, Science.

[21]  J. Mandel,et al.  Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome , 1991, Science.

[22]  C. Denny,et al.  Characterization of the BCR promoter in Philadelphia chromosome-positive and -negative cell lines , 1991, Molecular and cellular biology.

[23]  J. Idle,et al.  Is environmental carcinogenesis modulated by host polymorphism? , 1991, Mutation research.

[24]  K. Davies,et al.  Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome , 1991, Cell.

[25]  C. Petit,et al.  Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis , 1991, Nature.

[26]  J. Hemperly,et al.  Human N-cadherin: nucleotide and deduced amino acid sequence. , 1990, Nucleic acids research.

[27]  P. Goodfellow,et al.  N‐Cadherin Gene Maps to Human Chromosome 18 and Is Not Linked to the E‐Cadherin Gene , 1990, Journal of neurochemistry.

[28]  K. Geering,et al.  The sodium pump needs its β subunit , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[29]  S. Hoshino,et al.  A human homologue of the yeast GST1 gene codes for a GTP‐binding protein and is expressed in a proliferation‐dependent manner in mammalian cells. , 1989, The EMBO journal.

[30]  J. Lingrel,et al.  Characterization of two genes for the human Na,K-ATPase β subunit , 1989 .

[31]  K. Semba,et al.  Identification of two novel members of erbA superfamily by molecular cloning: the gene products of the two are highly related to each other. , 1988, Nucleic acids research.

[32]  N. Galjart,et al.  Expression of cDNA encoding the human “protective protein≓ associated with lysosomal β-galactosidase and neuraminidase: Homology to yeast proteases , 1988, Cell.

[33]  U. Francke,et al.  Chromosomal localization of human Na+,K+-ATPase α- and β-subunit genes , 1988 .

[34]  K. Suzuki,et al.  Gene organization of the small subunit of human calcium-activated neutral protease. , 1986, Nucleic acids research.

[35]  J. Erickson,et al.  Variation among human 28S ribosomal RNA genes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[36]  R. Newcombe,et al.  Sodium-potassium-ATPase and obesity. , 1984, The New England journal of medicine.

[37]  N. Morton,et al.  The marker (X) syndrome: a cytogenetic and genetic analysis , 1984, Annals of human genetics.

[38]  E. Beutler,et al.  Sodium-potassium-ATPase activity is influenced by ethnic origin and not by obesity. , 1983, The New England journal of medicine.

[39]  K. Morgan,et al.  Erythrocyte sodium-potassium-ATPase and sodium transport in obesity. , 1981, The New England journal of medicine.

[40]  D. Botstein,et al.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.

[41]  R. Strange,et al.  The human glutathione S-transferases: a case-control study of the incidence of the GST1 0 phenotype in patients with adenocarcinoma. , 1991, Carcinogenesis.

[42]  N. Shimizu,et al.  Four genes for the calpain family locate on four distinct human chromosomes. , 1990, Cytogenetics and cell genetics.

[43]  N. Heisterkamp,et al.  Unique organization of the human BCR gene promoter. , 1990, Nucleic acids research.

[44]  D. Ledbetter,et al.  Report of the committee on cytogenetic markers. , 1989, Cytogenetics and cell genetics.

[45]  P. Nowell,et al.  A minute chromosome in human chronic granulocytic leukemia , 1960 .