Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA. (Q34212647)

31 July 2017

Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA. (English)

1 reference

31 July 2017

Tamio Suzuki

1

1 reference

31 July 2017

Yoshinori Miyamura

series ordinal

2

1 reference

31 July 2017

Katsuhiko Inagaki

series ordinal

3

1 reference

31 July 2017

Yasushi Tomita

series ordinal

4

1 reference

31 July 2017

1 August 2003

1 reference

Journal of Dermatological Science

31 July 2017

1 reference

31 July 2017

32

1 reference

31 July 2017

2

1 reference

31 July 2017

131-136

1 reference

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

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Molecular bases of congenital hypopigmentary disorders in humans and oculocutaneous albinism 1 in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Molecular genetics of oculocutaneous albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Mutation of melanosome protein RAB38 in chocolate mice

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Tyrosinase and tyrosinase-related protein 1 require Rab7 for their intracellular transport

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Mutant Rab7 causes the accumulation of cathepsin D and cation-independent mannose 6-phosphate receptor in an early endocytic compartment

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Molecular cloning and expression analysis of the human Rab7 GTP-ase complementary deoxyribonucleic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Rab proteins as membrane organizers

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Rab GTPases, intracellular traffic and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0923-1811%2803%2900071-9

7 January 2021

10.1016/S0923-1811(03)00071-9

Identifiers

DOI

1 reference

31 July 2017

1 reference