(Q24316501)

1

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E I Rogaev

2

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Y Liang

3

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E A Rogaeva

4

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G Levesque

5

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M Ikeda

6

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H Chi

7

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C Lin

8

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G Li

9

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K Holman

10

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T Tsuda

11

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L Mar

12

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J F Foncin

13

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A C Bruni

14

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M P Montesi

15

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S Sorbi

16

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I Rainero

17

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L Pinessi

18

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L Nee

19

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I Chumakov

20

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D Pollen

21

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A Brookes

22

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P Sanseau

23

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R J Polinsky

24

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W Wasco

25

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H A Da Silva

26

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M A Perkicak-Vance

28

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R E Tanzi

29

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A D Roses

30

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P E Fraser

31

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J M Rommens

32

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P H St George-Hyslop

https://scigraph.springernature.com/pub.10.1038/375754a0

33

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language of work or name

English

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publication date

29 June 1995

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published in

Nature

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volume

375

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page(s)

754-60

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issue

6534

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exact match

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1 reference

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Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

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Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

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A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

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Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene.

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Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

1 reference

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Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.

1 reference

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Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3.

1 reference

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Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease.

1 reference

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Mutation of the gene for the human lysosomal serine protease cathepsin G is not the cause of aberrant APP processing in familial Alzheimer disease.

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A family with histologically confirmed Alzheimer's disease.

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Familial Alzheimer's disease in two kindreds of the same geographic and ethnic origin. A clinical and genetic study

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Genetic linkage studies in Alzheimer's disease families.

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Identification of the cystic fibrosis gene: genetic analysis

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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A transcription map of the region containing the Huntington disease gene

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Combining evolutionary information and neural networks to predict protein secondary structure

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A simple method for displaying the hydropathic character of a protein

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Basic local alignment search tool

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Mutation of a putative sperm membrane protein in Caenorhabditis elegans prevents sperm differentiation but not its associated meiotic divisions

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Alzheimer's disease and possible gene interaction.

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Normal and abnormal biology of the beta-amyloid precursor protein.

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Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia.

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Identification of a mutation in the gene causing hyperkalemic periodic paralysis

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The identification and suppression of inherited neurodegeneration in Caenorhabditis elegans

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The mec-4 gene is a member of a family of Caenorhabditis elegans genes that can mutate to induce neuronal degeneration.

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Potassium channel dysfunction in fibroblasts identifies patients with Alzheimer disease

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beta-Amyloid precursor protein metabolites and loss of neuronal Ca2+ homeostasis in Alzheimer's disease.

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Calcium ionophore increases amyloid beta peptide production by cultured cells.

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A second-generation linkage map of the human genome

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The 1993-94 Généthon human genetic linkage map

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Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

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Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library

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A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.

1 reference

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Continuum of overlapping clones spanning the entire human chromosome 21q.

1 reference

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A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

1 reference

7 January 2021