(Q24672022)

1

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L Conforti

2

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E A Buckmaster

3

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A Tarlton

4

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M C Brown

6

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M F Lyon

7

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V H Perry

Proceedings of the National Academy of Sciences of the United States of America

8

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language of work or name

English

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publication date

18 August 1998

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published in

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volume

95

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issue

17

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page(s)

9985-90

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describes a project that uses

ImageQuant

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC21448/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Bcl-2 overexpression prevents motoneuron cell body loss but not axonal degeneration in a mouse model of a neurodegenerative disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

The Effects of Unequal Crossing over at the Bar Locus in Drosophila

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

A gene affecting Wallerian nerve degeneration maps distally on mouse chromosome 4

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Construction and preliminary analysis of the ICRF human P1 library

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Molecular characterization of a new family with alpha-thalassemia-1 (--MA mutation).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Hypervariable minisatellite DNA is a hotspot for homologous recombination in human cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Yeast artificial chromosome cloning of a two-megabase-size contig within chromosomal band 18q21 establishes physical linkage between BCL2 and plasminogen activator inhibitor type-2.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

GDNF slows loss of motoneurons but not axonal degeneration or premature death of pmn/pmn mice.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Frequent rearrangements at minisatellite loci D1S7 (1p33-35), D7S22 (7q36-ter) and D12S11 (12q24.3-ter) in hepatitis B virus-positive hepatocellular carcinomas from Thai patients

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Characterization of the calcium-induced disruption of neurofilaments in rat peripheral nerve

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21448

Experiments on the Section of the Glossopharyngeal and Hypoglossal Nerves of the Frog, and Observations of the Alterations Produced Thereby in the Structure of Their Primitive Fibres

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Evidence that the Rate of Wallerian Degeneration is Controlled by a Single Autosomal Dominant Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Prolonged survival of transected nerve fibres in C57BL/Ola mice is an intrinsic characteristic of the axon

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

The role of non-resident cells in Wallerian degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Calcium-mediated degeneration of the axonal cytoskeleton in the Ola mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

The rate of Wallerian degeneration in cultured neurons from wild type and C57BL/WldS mice depends on time in culture and may be extended in the presence of elevated K+ levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Absence of Wallerian Degeneration does not Hinder Regeneration in Peripheral Nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Evidence that Very Slow Wallerian Degeneration in C57BL/Ola Mice is an Intrinsic Property of the Peripheral Nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Consequences of slow Wallerian degeneration for regenerating motor and sensory axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Impaired motor axon regeneration in the C57BL/Ola mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

High-resolution mapping of the genes Kcnb3 and Ly63 on distal mouse chromosome 4

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

THE BAR "GENE" A DUPLICATION

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Crosses of NOD mice with the related NON strain. A polygenic model for IDDM

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.9985

Identification of two genes on chromosome 4 that determine resistance to plasmacytoma induction in mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9707587

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.17.9985

1 reference

ADS bibcode

1998PNAS...95.9985C

0 references

1 reference

1 reference

PubMed publication ID

9707587

1 reference