(Q30471657)

English

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

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scholarly article

1 reference

Europe PubMed Central

17 September 2017

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

1 reference

Europe PubMed Central

17 September 2017

1 reference

based on heuristic

inferred from title

Philip Rosenstiel

3

1 reference

Europe PubMed Central

21 June 2017

author name string

A Ikeda

1

1 reference

Europe PubMed Central

17 September 2017

Q Y Zheng

2

1 reference

Europe PubMed Central

17 September 2017

T Maddatu

4

1 reference

Europe PubMed Central

17 September 2017

A R Zuberi

5

1 reference

Europe PubMed Central

17 September 2017

D C Roopenian

6

1 reference

Europe PubMed Central

17 September 2017

M A North

7

1 reference

Europe PubMed Central

17 September 2017

J K Naggert

8

1 reference

Europe PubMed Central

17 September 2017

K R Johnson

9

1 reference

Europe PubMed Central

17 September 2017

P M Nishina

10

1 reference

Europe PubMed Central

17 September 2017

publication date

1 September 1999

1 reference

Europe PubMed Central

17 September 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

17 September 2017

8

1 reference

Europe PubMed Central

17 September 2017

1761-1767

1 reference

Europe PubMed Central

17 September 2017

9

1 reference

Europe PubMed Central

17 September 2017

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

A major gene affecting age-related hearing loss in C57BL/6J mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Progression of cochlear and retinal degeneration in the tubby (rd5) mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

The role of neurotrophic factors in regulating the development of inner ear innervation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Permutation tests for multiple loci affecting a quantitative character

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

A candidate gene for the mouse mutation tubby

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Mice lacking brain-derived neurotrophic factor develop with sensory deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Neurotrophic molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Mapping mendelian factors underlying quantitative traits using RFLP linkage maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3249642

20 June 2018

Beta 2-microglobulin-deficient mice are protected from hypergammaglobulinemia and have defective antibody responses because of increased IgG catabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele-specific PCR assays for the tub and cpefat mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of DNA from biological specimens without extraction with phenol

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/8.9.1761

1 reference

Europe PubMed Central

17 September 2017

1 reference

Europe PubMed Central

17 September 2017

1 reference

Europe PubMed Central

17 September 2017

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