(Q33199783)

23 July 2017

title

Systematic genome-wide approach to positional candidate cloning for identification of novel human disease genes (English)

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23 July 2017

Kiyosawa H

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23 July 2017

Kawashima T

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23 July 2017

Silva D

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23 July 2017

Petrovsky N

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23 July 2017

Hasegawa Y

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23 July 2017

Sakai K

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23 July 2017

Hayashizaki Y

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23 July 2017

publication date

1 March 2004

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Internal Medicine Journal

23 July 2017

published in

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23 July 2017

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23 July 2017

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23 July 2017

page(s)

79-90

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Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

23 July 2017

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Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients

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Cloning and gene mapping of the chromosome 13q14 region deleted in chronic lymphocytic leukemia

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Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity

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Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM

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Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals

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A gene for Meckel syndrome maps to chromosome 11q13.

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Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes

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A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36

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Construction of a physical and transcript map for a 1-Mb genomic region containing the urofacial (Ochoa) syndrome gene on 10q23-q24 and localization of the disease gene within two overlapping BAC clones (<360 kb).

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Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

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A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

21 January 2018

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Cytogenetic mapping of a novel locus for type II Waardenburg syndrome

21 January 2018

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Unlocking the mechanisms of transcription factor YY1: are chromatin modifying enzymes the key?

21 January 2018

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IRE1-mediated unconventional mRNA splicing and S2P-mediated ATF6 cleavage merge to regulate XBP1 in signaling the unfolded protein response

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Hepatitis B virus pX interacts with HBXAP, a PHD finger protein to coactivate transcription

21 January 2018

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Structural basis for recruitment of CBP/p300 by hypoxia-inducible factor-1 alpha

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The neprilysin (NEP) family of zinc metalloendopeptidases: genomics and function

21 January 2018

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Neprilysin degrades both amyloid beta peptides 1-40 and 1-42 most rapidly and efficiently among thiorphan- and phosphoramidon-sensitive endopeptidases

21 January 2018

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Characterization of a novel type of human microsomal 3alpha -hydroxysteroid dehydrogenase: unique tissue distribution and catalytic properties

21 January 2018

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GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma

21 January 2018

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Initial sequencing and analysis of the human genome

21 January 2018

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The Sequence of the Human Genome

21 January 2018

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Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)

21 January 2018

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Characterization of colorectal-cancer-related cDNA clones obtained by subtractive hybridization screening

21 January 2018

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A Comparison of the Celera and Ensembl Predicted Gene Sets Reveals Little Overlap in Novel Genes

21 January 2018

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

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Loss of heterozygosity in sporadic oesophageal tumors in the tylosis oesophageal cancer (TOC) gene region of chromosome 17q

21 January 2018

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Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3

21 January 2018

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Positional cloning moves from perditional to traditional

21 January 2018

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Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

21 January 2018

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Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints

21 January 2018

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Mapping an endometrial cancer tumor suppressor gene at 10q25 and development of a bacterial clone contig for the consensus deletion interval

21 January 2018

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Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA locus (SCA8) on 10q24

21 January 2018

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Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity

21 January 2018

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Refinement of the Smallest Commonly Deleted Segment of Chromosome 20 in Malignant Myeloid Diseases and Development of a PAC-Based Physical and Transcription Map

21 January 2018

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Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1444-0903.2004.00581.X

Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1444-0903.2004.00581.X

Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1444-0903.2004.00581.X

10.1111/J.1444-0903.2004.00581.X

21 January 2018

Identifiers

DOI

1 reference

23 July 2017

1 reference