(Q73256820)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11101839%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

Dominant modifier DFNM1 suppresses recessive deafness DFNB26 (English)

1 reference

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2 November 2019

1 reference

6

1 reference

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2 November 2019

9

T B Friedman

1 reference

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2 November 2019

author name string

S Riazuddin

1

1 reference

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2 November 2019

C M Castelein

2

1 reference

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2 November 2019

Z M Ahmed

3

1 reference

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2 November 2019

A K Lalwani

4

1 reference

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2 November 2019

M A Mastroianni

5

1 reference

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2 November 2019

T N Smith

7

1 reference

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2 November 2019

N A Liburd

8

1 reference

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2 November 2019

A J Griffith

10

1 reference

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2 November 2019

S Riazuddin

11

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2 November 2019

E R Wilcox

12

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2 November 2019

publication date

1 December 2000

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2 November 2019

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2 November 2019

volume

26

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2 November 2019

page(s)

431-434

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2 November 2019

issue

4

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https://scigraph.springernature.com/pub.10.1038/82558

2 November 2019

exact match

0 references

cites work

Genetic epidemiology of hearing impairment

1 reference

7 January 2021

Genetic causes of hearing loss

1 reference

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

7 January 2021

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

1 reference

7 January 2021

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

1 reference

7 January 2021

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

7 January 2021

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.

1 reference

7 January 2021

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

1 reference

7 January 2021

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.

1 reference

7 January 2021

Genomic organization and chromosome localization of the murine homeobox gene Pmx.

1 reference

7 January 2021

Human cDNA sequence homologous to the mouse LLRep3 gene family

1 reference

7 January 2021

Grb2-associated binder-1 mediates phosphatidylinositol 3-kinase activation and the promotion of cell survival by nerve growth factor

1 reference

7 January 2021

Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI

1 reference

7 January 2021

Modifier genes of hereditary hearing loss

1 reference

7 January 2021

Candidate locus for a nuclear modifier gene for maternally inherited deafness

1 reference

7 January 2021

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

1 reference

7 January 2021

Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss

1 reference

7 January 2021

Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.

1 reference

7 January 2021

A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1.

1 reference

7 January 2021

A common polymorphism acts as an intragenic modifier of mutant p53 behaviour

1 reference

7 January 2021

Evidence for regulation of the PTEN tumor suppressor by a membrane-localized multi-PDZ domain containing scaffold protein MAGI-2

1 reference

7 January 2021

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

1 reference

7 January 2021

Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.

1 reference

7 January 2021

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

1 reference

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

7 January 2021

Mutation of human short tandem repeats

1 reference

7 January 2021

Identifiers

DOI

10.1038/82558

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11101839%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference