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Bcl2 Regulation by the Melanocyte Master Regulator Mitf Modulates Lineage Survival and Melanoma Cell Viability

Cell, 2002-06, Vol.109 (6), p.707-718

2002

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Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited

Development (Cambridge), 2002-07, Vol.129 (14), p.3349-3357

2002

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Dominant role of the niche in melanocyte stem-cell fate determination

Nature (London), 2002-04, Vol.416 (6883), p.854-860

2002

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A three-base-pair deletion in the peripherin- RDS gene in one form of retinitis pigmentosa

Nature (London), 1991-12, Vol.354 (6353), p.478-480

1991

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Activation of the Receptor Tyrosine Kinase Kit Is Required for the Proliferation of Melanoblasts in the Mouse Embryo

Developmental biology, 1997-12, Vol.192 (1), p.99-107

1997

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Melanocortin 1 receptor variation in the domestic dog

Mammalian genome, 2000-01, Vol.11 (1), p.24-30

2000

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Widespread tangential dispersion and extensive cell death during early neurogenesis in the mouse neocortex

Developmental biology, 2004-03, Vol.267 (1), p.109-118

2004

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Functional variation of MC1R alleles from red-haired individuals

Human molecular genetics, 2001-10, Vol.10 (21), p.2397-2402

2001

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A late wave of melanoblast differentiation and rostrocaudal migration revealed in patch and rump-white embryos

Mechanisms of development, 2000-04, Vol.92 (2), p.135-143

2000

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Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

Nature genetics, 1993-05, Vol.4 (1), p.54-58

1993

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MGF (KIT Ligand) Is a Chemokinetic Factor for Melanoblast Migration into Hair Follicles

Developmental biology, 2000-09, Vol.225 (2), p.424-436

2000

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The Human Serum Amyloid A Protein (SAA) Superfamily Gene Cluster: Mapping to Chromosome 11p15.1 by Physical and Genetic Linkage Analysis

Genomics (San Diego, Calif.), 1994-01, Vol.19 (2), p.221-227

1994

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comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23

Mammalian genome, 2000, Vol.11 (1), p.58-63

2000

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The Mouse Cer1 (Cerberus related or homologue) Gene Is Not Required for Anterior Pattern Formation

Developmental biology, 1999-09, Vol.213 (1), p.202-206

1999

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Deficiency of Trp53 rescues the male fertility defects of Kit(W-v) mice but has no effect on the survival of melanocytes and mast cells

Developmental biology, 1999-11, Vol.215 (1), p.78

1999

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Melanocortin receptors and antagonists regulate pigmentation and body weight

BioEssays, 1998-08, Vol.20 (8), p.603-606

1998

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Deficiency of Trp53 Rescues the Male Fertility Defects of KitW-v Mice but Has No Effect on the Survival of Melanocytes and Mast Cells

Developmental biology, 1999-11, Vol.215 (1), p.78-90

1999

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Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig

Genome research, 1996-04, Vol.6 (4), p.255-266

1996

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Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree

Genomics (San Diego, Calif.), 1992-11, Vol.14 (3), p.805-807

1992

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Dinucleotide repeat polymorphism at the T cell receptor δ locus (TCRD)

Nucleic acids research, 1991-04, Vol.19 (8), p.1959-1959

1991

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Polymorphic variation within "conserved" sequences at the 3′ end of the human RDS gene which results in amino acid substitutions

Human mutation, 1992, Vol.1 (3), p.240-247

1992

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Autosomal dominant retinitis pigmentosa: Localization of a disease gene (RP6) to the short arm of chromosome 6

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.870-874

1991

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Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

Human mutation, 1996, Vol.8 (1), p.57-63

1996

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Targeting human hair follicles

Molecular medicine today (Regul. ed.), 2000-07, Vol.6 (7), p.263-263

Jordan, Siobhán A

2000

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Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin

American journal of human genetics, 1992-03, Vol.50 (3), p.634-639

1992

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Bcl2 Regulation by the Melanocyte Master Regulator Mitf Modulates Lineage Survival and Melanoma Cell Viability

Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited

Dominant role of the niche in melanocyte stem-cell fate determination

A three-base-pair deletion in the peripherin- RDS gene in one form of retinitis pigmentosa

Activation of the Receptor Tyrosine Kinase Kit Is Required for the Proliferation of Melanoblasts in the Mouse Embryo

Melanocortin 1 receptor variation in the domestic dog

Widespread tangential dispersion and extensive cell death during early neurogenesis in the mouse neocortex

Functional variation of MC1R alleles from red-haired individuals

A late wave of melanoblast differentiation and rostrocaudal migration revealed in patch and rump-white embryos

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

MGF (KIT Ligand) Is a Chemokinetic Factor for Melanoblast Migration into Hair Follicles

The Human Serum Amyloid A Protein (SAA) Superfamily Gene Cluster: Mapping to Chromosome 11p15.1 by Physical and Genetic Linkage Analysis

comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23

The Mouse Cer1 (Cerberus related or homologue) Gene Is Not Required for Anterior Pattern Formation

Deficiency of Trp53 rescues the male fertility defects of Kit(W-v) mice but has no effect on the survival of melanocytes and mast cells

Melanocortin receptors and antagonists regulate pigmentation and body weight

Deficiency of Trp53 Rescues the Male Fertility Defects of KitW-v Mice but Has No Effect on the Survival of Melanocytes and Mast Cells

Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig

Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree

Dinucleotide repeat polymorphism at the T cell receptor δ locus (TCRD)

Polymorphic variation within "conserved" sequences at the 3′ end of the human RDS gene which results in amino acid substitutions

Autosomal dominant retinitis pigmentosa: Localization of a disease gene (RP6) to the short arm of chromosome 6

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

Targeting human hair follicles

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin

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