(Q22254278)

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Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs

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scholarly article

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Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs (English)

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Family with sequence similarity 114 member A2

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GOA release 2020-03-11

purine nucleotide binding

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GOA release 2020-03-11

Jacqueline Boultwood

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J Boultwood

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J

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Boultwood

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8 February 2023

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C Fidler

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C

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Fidler

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8 February 2023

A J Strickson

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A J

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Strickson

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8 February 2023

F Watkins

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F

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Watkins

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8 February 2023

M Kostrzewa

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M

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Kostrzewa

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8 February 2023

R J Jaju

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R J

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Jaju

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8 February 2023

U Müller

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U

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Müller

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8 February 2023

J S Wainscoat

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J S

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Wainscoat

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8 February 2023

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publication date

15 May 2000

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66

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1

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26-34

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Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

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Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

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A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Novel genes mapping to the critical region of the 5q- syndrome.

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Assignment of 48 ESTs to Chromosome 13 Band q14.3 and Expression Pattern for ESTs Located in the Core Region Deleted in B-CLL

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

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The P-loop--a common motif in ATP- and GTP-binding proteins

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Identification and cloning of a novel cellular protein Naf1, Nef-associated factor 1, that increases cell surface CD4 expression

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF-1

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Electrostatic control of GTP and GDP binding in the oncoprotein p21ras

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct haematological disorder with deletion of long arm of no. 5 chromosome

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Positional cloning moves from perditional to traditional

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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dbEST--database for "expressed sequence tags"

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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ESTablishing a human transcript map

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Integrated physical and transcript map of 5q31.3-qter

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Monosomy 7 in Granulocytes and Monocytes in Myelodysplastic Syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

The interleukin 3 gene is located on human chromosome 5 and is deleted in myeloid leukemias with a deletion of 5q

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion mutation analysis of the mutS gene in Escherichia coli

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Genome maps 7. The human transcript map. Wall chart

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Human renin gene assigned to chromosome band 1q42 by in situ hybridization

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Report of the second international workshop on human chromosome 5 mapping.

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https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

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Epidemiological and etiological aspects of myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2000.6193

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1006/GENO.2000.6193

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