Analysis of ocular hypopigmentation in Rab38cht/cht mice (Q36008833)

11 August 2017

Analysis of ocular hypopigmentation in Rab38cht/cht mice (English)

1 reference

11 August 2017

Arvydas Maminishkis

12

0 references

William J Pavan

object named as

William J Pavan

15

0 references

Chi-Chao Chan

3

object named as

Chi-Chao Chan

1 reference

11 August 2017

Brian P Brooks

1

1 reference

11 August 2017

Denise M Larson

2

1 reference

11 August 2017

Sten Kjellstrom

4

1 reference

11 August 2017

Richard S Smith

5

1 reference

11 August 2017

Mary A Crawford

6

1 reference

11 August 2017

Lynn Lamoreux

7

1 reference

11 August 2017

Marjan Huizing

8

1 reference

11 August 2017

Richard Hess

9

1 reference

11 August 2017

Xiaodong Jiao

10

1 reference

11 August 2017

J Fielding Hejtmancik

11

1 reference

11 August 2017

Simon W M John

13

1 reference

11 August 2017

Ronald Bush

14

1 reference

11 August 2017

language of work or name

English

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publication date

1 September 2007

1 reference

Investigative Ophthalmology Visual Science

11 August 2017

1 reference

11 August 2017

48

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11 August 2017

9

1 reference

11 August 2017

3905-3913

1 reference

Rab38 and Rab32 control post-Golgi trafficking of melanogenic enzymes

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

The rat Ruby ( R) locus is Rab38: identical mutations in Fawn-hooded and Tester-Moriyama rats derived from an ancestral Long Evans rat sub-strain

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

The color loci of mice--a genetic century

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Hermansky-Pudlak syndrome: vesicle formation from yeast to man.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Disorders of vesicles of lysosomal lineage: the Hermansky-Pudlak syndromes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Mutation of melanosome protein RAB38 in chocolate mice

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Rab GTPases, intracellular traffic and disease.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Tyrp1 and oculocutaneous albinism type 3

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Rab proteins as membrane organizers

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Serological cloning of a melanocyte rab guanosine 5'-triphosphate-binding protein and a chromosome condensation protein from a melanoma complementary DNA library

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3"

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Characterization of TRP-1 mRNA levels in dominant and recessive mutations at the mouse brown (b) locus.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

The molecular basis of brown, an old mouse mutation, and of an induced revertant to wild type

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

The mammalian Rab family of small GTPases: definition of family and subfamily sequence motifs suggests a mechanism for functional specificity in the Ras superfamily

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1).

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Modulation of melanogenic protein expression during the switch from eu- to pheomelanogenesis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1989767

Electroretinographic findings in human oculocutaneous albinism

23 September 2018

1 reference

12 December 2020

Mouse models of Hermansky Pudlak syndrome: a review

1 reference

12 December 2020

The Electroretinogram in Albinos and Carriers of the Ocular Albino Trait

1 reference

12 December 2020

EFFECTS OF THE LIGHT MUTATION OF MOUSE COAT COLOR ON EYE PIGMENTATION

1 reference

12 December 2020

The mouse ocular albinism 1 gene product is an endolysosomal protein

1 reference

12 December 2020

Genetic mapping and characterization of the bleeding disorder in the fawn-hooded hypertensive rat

1 reference

12 December 2020

A new form of albinism

1 reference

12 December 2020

The electroretinogram of albinos

1 reference

12 December 2020

Identifiers

DOI

10.1167/IOVS.06-1464

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

17724166

1 reference