(Q74237817)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11464241%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11464241%20AND%20SRC:MED&resulttype=core&format=json

Hereditary inclusion body myopathy

9 November 2019

main subject

1 reference

Eisenberg I

1

1 reference

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9 November 2019

Hochner H

2

1 reference

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9 November 2019

Shemesh M

3

1 reference

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9 November 2019

Levi T

4

1 reference

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9 November 2019

Potikha T

5

1 reference

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9 November 2019

Sadeh M

6

1 reference

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9 November 2019

Argov Z

7

1 reference

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9 November 2019

Jackson CL

8

1 reference

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9 November 2019

Mitrani-Rosenbaum S

9

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9 November 2019

publication date

1 July 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11464241%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

9 November 2019

published in

1 reference

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9 November 2019

volume

9

1 reference

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9 November 2019

issue

7

1 reference

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9 November 2019

page(s)

501-509

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200665

9 November 2019

exact match

0 references

cites work

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

1 reference

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7 January 2021

Vacuolar myopathy sparing the quadriceps.

1 reference

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7 January 2021

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Facial weakness in hereditary inclusion body myopathies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Fine-structure mapping of the hereditary inclusion body myopathy locus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Involvement of the short arm of the derivative chromosome 9 in Philadelphia-positive acute lymphoblastic leukemia

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7 January 2021

Biologic and molecular characterization of non-Hodgkin's lymphoma.

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7 January 2021

Frequent allelic loss on chromosome 9 in hepatocellular carcinoma.

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7 January 2021

Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Distal Hereditary Motor Neuronopathy of the Jerash Type

1 reference

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7 January 2021

A physical map of 30,000 human genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Complete nucleotide sequence of the adult skeletal isoform of human skeletal muscleβ-tropomyosin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Sequence and domain structure of talin

1 reference

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7 January 2021

Characterization of the human talin (TLN) gene: genomic structure, chromosomal localization, and expression pattern

1 reference

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7 January 2021

Luman, a new member of the CREB/ATF family, binds to herpes simplex virus VP16-associated host cellular factor

1 reference

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7 January 2021

Regulation of matrix metalloproteinase-9 and inhibition of tumor invasion by the membrane-anchored glycoprotein RECK

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7 January 2021

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Molecular nature of calicin, a major basic protein of the mammalian sperm head cytoskeleton.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Immunohistochemical study of clathrin in distal myopathy with rimmed vacuoles

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Genetics of inclusion body myopathies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Integrated high-resolution BAC, P1, and transcript map of the CHH region in chromosome 9p13.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200665

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200665

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11464241%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference