Individual variation in protein-coding sequences of human genome (Q33928607)

30 July 2017

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title

Individual variation in protein-coding sequences of human genome (English)

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30 July 2017

7

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30 July 2017

Sunyaev S

1

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30 July 2017

Hanke J

2

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30 July 2017

Brett D

3

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30 July 2017

Aydin A

4

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30 July 2017

Zastrow I

5

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30 July 2017

Lathe W

6

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30 July 2017

Reich J

8

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30 July 2017

publication date

1 January 2000

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Advances in Protein Chemistry

30 July 2017

published in

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30 July 2017

volume

54

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30 July 2017

page(s)

409-437

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

30 July 2017

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Reliable identification of large numbers of candidate SNPs from public EST data

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

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It's raining SNPs, hallelujah?

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Population genetics--making sense out of sequence

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Accessing genetic information with high-density DNA arrays.

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Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

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Variations on a theme: cataloging human DNA sequence variation

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An estimate of unique DNA sequence heterozygosity in the human genome

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Base-calling of automated sequencer traces using phred. I. Accuracy assessment

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Consed: a graphical tool for sequence finishing

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Resequencing and mutational analysis using oligonucleotide microarrays

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7 January 2021

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays

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7 January 2021

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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7 January 2021

Alternative splicing of human genes: more the rule than the exception?

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7 January 2021

Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms

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7 January 2021

Why pharmacogenomics? Why now?

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7 January 2021

A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin

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7 January 2021

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

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Expression of epidermal growth factor receptor and CD44 splicing variants sharing exons 6 and 9 on gastric and esophageal carcinomas: a two-color flow-cytometric analysis

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High density synthetic oligonucleotide arrays

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7 January 2021

Adaptive protein evolution at the Adh locus in Drosophila

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7 January 2021

Intraspecific nuclear DNA variation in Drosophila

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7 January 2021

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

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7 January 2021

SCLIP: a novel SCG10-like protein of the stathmin family expressed in the nervous system

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7 January 2021

Sickle cell anemia, a molecular disease

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7 January 2021

Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the menkes protein and produces the occipital horn syndrome

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7 January 2021

DNA chips: state-of-the art.

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7 January 2021

The future of genetic studies of complex human diseases

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7 January 2021

A novel presenilin-2 splice variant in human Alzheimer's disease brain tissue

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7 January 2021

A Gene Map of the Human Genome

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7 January 2021

Pieces of the puzzle: expressed sequence tags and the catalog of human genes

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7 January 2021

Split genes and RNA splicing

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7 January 2021

Association of a human G-protein beta3 subunit variant with hypertension

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7 January 2021

Alternatively spliced mdm2 transcripts with loss of p53 binding domain sequences: transforming ability and frequent detection in human cancer.

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7 January 2021

Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults

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7 January 2021

Overlapping genomic sequences: a treasure trove of single-nucleotide polymorphisms

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7 January 2021

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

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7 January 2021

Direct allelic variation scanning of the yeast genome.

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7 January 2021

A comparison of expressed sequence tags (ESTs) to human genomic sequences

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7 January 2021

A DNA cycle sequencing reaction that minimizes compressions on automated fluorescent sequencers

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7 January 2021

Nuclear DNA diversity in worldwide distributed human populations

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7 January 2021

10.1016/S0065-3233(00)54012-1

Identifiers

DOI

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30 July 2017

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