(Q44731103)

English

A form of albinism in cattle is caused by a tyrosinase frameshift mutation

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 December 2017

A form of albinism in cattle is caused by a tyrosinase frameshift mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

1 reference

based on heuristic

inferred from title

Merete Fredholm

6

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

author name string

Sheila M Schmutz

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Tom G Berryere

2

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Daniel C Ciobanu

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Alan J Mileham

4

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Barbara H Schmidtz

5

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

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Europe PubMed Central

PubMed publication ID

5 December 2017

15

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Europe PubMed Central

PubMed publication ID

5 December 2017

1

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Europe PubMed Central

PubMed publication ID

5 December 2017

62-67

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Europe PubMed Central

PubMed publication ID

5 December 2017

Tyrosinase gene variants in different rabbit strains.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis of the platinum (cp) mutation, a model for oculocutaneous albinism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete albinism in beef Shorthorn calves

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous appearance of albinos in the brown Swiss cattle breed

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the bovine albino locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA-based prenatal diagnosis of a Korean family with tyrosinase-related oculocutaneous albinism (OCA1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete Albinism in a Guernsey Calf

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of copper binding by human tyrosinase.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage mapping of the tyrosinase gene to bovine chromosome 29.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic control of pigmentation in mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA marker-assisted selection of the polled condition in Charolais cattle

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of bovine LYST gene and identification of a missense mutation associated with Chediak-Higashi syndrome of cattle

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): A model for understanding the molecular biology of melanin formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an autosome to X chromosome translocation in the domestic cow

1 reference

https://pubmed.ncbi.nlm.nih.gov/14727143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00335-002-2249-5

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

ResearchGate publication ID

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