-
1
-
-
1842421129
-
The melanosome as a model to study organelle motility in mammals
-
Barral DC, Seabra MC. 2004. The melanosome as a model to study organelle motility in mammals. Pigment Cell Res. 17:111-118.
-
(2004)
Pigment Cell Res
, vol.17
, pp. 111-118
-
-
Barral, D.C.1
Seabra, M.C.2
-
2
-
-
0040120659
-
Canine hereditary black hair follicular dysplasia and colour mutant alopecia, Clinical and histopathological aspects
-
Von Tscharner C, Halliwell REW, eds. Philadelphia: Baillière Tindall
-
Carlotti DN. 1990. Canine hereditary black hair follicular dysplasia and colour mutant alopecia. Clinical and histopathological aspects. In: Von Tscharner C, Halliwell REW, eds. Advances in veterinary dermatology. vol. 1, Philadelphia: Baillière Tindall, p. 43-46.
-
(1990)
Advances in Veterinary Dermatology
, vol.1
, pp. 43-46
-
-
Carlotti, D.N.1
-
3
-
-
34548426013
-
A non-coding melanophilin gene (MLPH) SNP at the splice donor of exon 1 (c.-22G.A) represents a candidate causal mutation for coat color dilution in dogs
-
Drögemüller C, Philipp U, Haase B, Günzel-Apel AR, Leeb T. 2007. A non-coding melanophilin gene (MLPH) SNP at the splice donor of exon 1 (c.-22G.A) represents a candidate causal mutation for coat color dilution in dogs. J Hered. 98:468-473.
-
(2007)
J Hered
, vol.98
, pp. 468-473
-
-
Drögemüller, C.1
Philipp, U.2
Haase, B.3
Günzel-Apel, A.R.4
Leeb, T.5
-
4
-
-
68149095886
-
Dysplastic diseases of the adnexa: Color dilution alopecia and black hair follicular dysplasia
-
Gross TL, Ihrke PJ, Walder EJ, Affolter VK, eds., 2nd ed. Oxford (UK): Blackwell Science Ltd
-
Gross TL, Ihrke PJ, Walder EJ, Affolter VK. 2005. Dysplastic diseases of the adnexa: color dilution alopecia and black hair follicular dysplasia. In: Gross TL, Ihrke PJ, Walder EJ, Affolter VK, eds. Skin diseases of the dog and cat: clinical and histopathological diagnosis, 2nd ed. Oxford (UK): Blackwell Science Ltd. p. 518-522.
-
(2005)
Skin Diseases of the Dog and Cat: Clinical and Histopathological Diagnosis
, pp. 518-522
-
-
Gross, T.L.1
Ihrke, P.J.2
Walder, E.J.3
Affolter, V.K.4
-
5
-
-
0012370196
-
Black hair follicular dysplasia in black and white saluki dogs: Differentiation from color mutant alopecia in the doberman pinscher by microscopic examination of hairs
-
Hargis AM, Brignac MM, Al-Bagdadi FAK, Muggli F, Mundell A. 1991. Black hair follicular dysplasia in black and white saluki dogs: differentiation from color mutant alopecia in the doberman pinscher by microscopic examination of hairs. Vet Dermatol. 2:69-83.
-
(1991)
Vet Dermatol
, vol.2
, pp. 69-83
-
-
Hargis, A.M.1
Brignac, M.M.2
Al-Bagdadi, F.A.K.3
Muggli, F.4
Mundell, A.5
-
6
-
-
22144461400
-
A guide to assessing damage response pathways of the hair follicle: Lessons from cyclophosphamide- induced alopecia in mice
-
Hendrix S, Handjiski B, Peters EM, Paus R. 2005. A guide to assessing damage response pathways of the hair follicle: lessons from cyclophosphamide- induced alopecia in mice. J Invest Dermatol. 125:42-51.
-
(2005)
J Invest Dermatol
, vol.125
, pp. 42-51
-
-
Hendrix, S.1
Handjiski, B.2
Peters, E.M.3
Paus, R.4
-
7
-
-
33750520133
-
A coiled-coil domain of melanophilin is essential for Myosin Va recruitment and melanosome transport in melanocytes
-
Hume AN, Tarafder AK, Ramalho JS, Sviderskaya EV, Seabra MC. 2006. A coiled-coil domain of melanophilin is essential for Myosin Va recruitment and melanosome transport in melanocytes. Mol Biol Cell. 17:4720-4735.
-
(2006)
Mol Biol Cell
, vol.17
, pp. 4720-4735
-
-
Hume, A.N.1
Tarafder, A.K.2
Ramalho, J.S.3
Sviderskaya, E.V.4
Seabra, M.C.5
-
8
-
-
34948826453
-
Rab27a and MyoVa are the primary Mlph interactors regulating melanosome transport in melanocytes
-
Hume AN, Ushakov DS, Tarafder AK, Ferenczi MA, Seabra MC. 2007. Rab27a and MyoVa are the primary Mlph interactors regulating melanosome transport in melanocytes. J Cell Sci. 120:3111-3122.
-
(2007)
J Cell Sci
, vol.120
, pp. 3111-3122
-
-
Hume, A.N.1
Ushakov, D.S.2
Tarafder, A.K.3
Ferenczi, M.A.4
Seabra, M.C.5
-
9
-
-
33751084845
-
A homozygous singlebase deletion in MLPH causes the dilute coat color phenotype in the domestic cat
-
Ishida Y, David VA, Eizirik E, Schäffer AA, Neelam BA, Roelke ME, Hannah SS, O'Brien SJ, Menotti-Raymond M. 2006. A homozygous singlebase deletion in MLPH causes the dilute coat color phenotype in the domestic cat. Genomics. 88:698-705.
-
(2006)
Genomics
, vol.88
, pp. 698-705
-
-
Ishida, Y.1
David, V.A.2
Eizirik, E.3
Schäffer, A.A.4
Neelam, B.A.5
Roelke, M.E.6
Hannah, S.S.7
O'Brien, S.J.8
Menotti-Raymond, M.9
-
12
-
-
0035964395
-
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice
-
Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA. 2001. Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice. Proc Natl Acad Sci U S A. 98:10238-10243.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 10238-10243
-
-
Matesic, L.E.1
Yip, R.2
Reuss, A.E.3
Swing, D.A.4
O'Sullivan, T.N.5
Fletcher, C.F.6
Copeland, N.G.7
Jenkins, N.A.8
-
13
-
-
33750691665
-
An overview on congenital alopecia in domestic animals
-
Mecklenburg L. 2006. An overview on congenital alopecia in domestic animals. Vet Dermatol. 17:393-410.
-
(2006)
Vet Dermatol
, vol.17
, pp. 393-410
-
-
Mecklenburg, L.1
-
14
-
-
0042388106
-
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
-
Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. 2003. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). J Clin Invest. 112:450-456.
-
(2003)
J Clin Invest
, vol.112
, pp. 450-456
-
-
Ménasché, G.1
Ho, C.H.2
Sanal, O.3
Feldmann, J.4
Tezcan, I.5
Ersoy, F.6
Houdusse, A.7
Fischer, A.8
De Saint Basile, G.9
-
15
-
-
26444448038
-
Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs
-
Philipp U, Hamann H, Mecklenburg L, Nishino S, Mignot E, Günzel-Apel AR, Schmutz SM, Leeb T. 2005. Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs. BMC Genet. 6:34.
-
(2005)
BMC Genet
, vol.6
, pp. 34
-
-
Philipp, U.1
Hamann, H.2
Mecklenburg, L.3
Nishino, S.4
Mignot, E.5
Günzel-Apel, A.R.6
Schmutz, S.M.7
Leeb, T.8
-
16
-
-
26444444498
-
Chromosomal assignment of the canine melanophilin gene (MLPH): A candidate gene for coat color dilution in Pinschers
-
Philipp U, Quignon P, Scott A, Andre C, Breen M, Leeb T. 2005. Chromosomal assignment of the canine melanophilin gene (MLPH): A candidate gene for coat color dilution in Pinschers. J Hered. 96:774-776.
-
(2005)
J Hered
, vol.96
, pp. 774-776
-
-
Philipp, U.1
Quignon, P.2
Scott, A.3
Andre, C.4
Breen, M.5
Leeb, T.6
-
17
-
-
36749093467
-
Genes affecting coat colour and pattern in domestic dogs: A review
-
Schmutz SM, Berryere TG. 2007. Genes affecting coat colour and pattern in domestic dogs: A review. Anim Genet. 38:539-549.
-
(2007)
Anim Genet
, vol.38
, pp. 539-549
-
-
Schmutz, S.M.1
Berryere, T.G.2
-
18
-
-
0032186390
-
Black hair follicular dysplasia, an autosomal recessive condition in dogs
-
Schmutz SM, Moker JS, Clark EG, Shewfelt R. 1998. Black hair follicular dysplasia, an autosomal recessive condition in dogs. Can Vet J. 39:644-646.
-
(1998)
Can Vet J
, vol.39
, pp. 644-646
-
-
Schmutz, S.M.1
Moker, J.S.2
Clark, E.G.3
Shewfelt, R.4
-
20
-
-
33646533935
-
Black hair follicular dysplasia in Large Munsterlander dogs: Clinical, histological and ultrastructural features
-
von Bomhard W, Mauldin EA, Schmutz SM, Leeb T, Casal ML. 2006. Black hair follicular dysplasia in Large Munsterlander dogs: clinical, histological and ultrastructural features. Vet Dermatol. 17:182-188.
-
(2006)
Vet Dermatol
, vol.17
, pp. 182-188
-
-
Von Bomhard, W.1
Mauldin, E.A.2
Schmutz, S.M.3
Leeb, T.4
Casal, M.L.5
|