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1
POT1 loss-of-function variants predispose to familial melanoma
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Artigo
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POT1 loss-of-function variants predispose to familial melanoma

Robles-Espinoza, Carla Daniela ; Harland, Mark ; Ramsay, Andrew J ; Aoude, Lauren G ; Quesada, Víctor ; Ding, Zhihao ; Pooley, Karen A ; Pritchard, Antonia L ; Tiffen, Jessamy C ; Petljak, Mia ; Palmer, Jane M ; Symmons, Judith ; Johansson, Peter ; Stark, Mitchell S ; Gartside, Michael G ; Snowden, Helen ; Montgomery, Grant W ; Martin, Nicholas G ; Liu, Jimmy Z ; Choi, Jiyeon ; Makowski, Matthew ; Brown, Kevin M ; Dunning, Alison M ; Keane, Thomas M ; López-Otín, Carlos ; Gruis, Nelleke A ; Hayward, Nicholas K ; Bishop, D Timothy ; Newton-Bishop, Julia A ; Adams, David J

Nature genetics, 2014-05, Vol.46 (5), p.478-481 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Characterization of the Melanoma miRNAome by Deep Sequencing
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Artigo
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Characterization of the Melanoma miRNAome by Deep Sequencing

Stark, Mitchell S ; Tyagi, Sonika ; Nancarrow, Derek J ; Boyle, Glen M ; Cook, Anthony L ; Whiteman, David C ; Parsons, Peter G ; Schmidt, Christopher ; Sturm, Richard A ; Hayward, Nicholas K Soyer, H. Peter

PloS one, 2010-03, Vol.5 (3), p.e9685-e9685 [Periódico revisado por pares]

United States: Public Library of Science

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3
A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color
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Artigo
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A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

Sturm, Richard A. ; Duffy, David L. ; Zhao, Zhen Zhen ; Leite, Fabio P.N. ; Stark, Mitchell S. ; Hayward, Nicholas K. ; Martin, Nicholas G. ; Montgomery, Grant W.

American journal of human genetics, 2008-02, Vol.82 (2), p.424-431 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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4
Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing
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Artigo
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Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing

STARK, Mitchell S ; WOODS, Susan L ; ELLIS, Jonathan J ; REID, Jeffrey ; ZISMANN, Victoria ; TYAGI, Sonika ; MUZNY, Donna ; NEWSHAM, Irene ; YUANQING WU ; PALMER, Jane M ; POLLAK, Thomas ; YOUNGKIN, David ; GARTSIDE, Michael G ; BROOKS, Bradford R ; LANAGAN, Catherine ; SCHMIDT, Christopher W ; KOBE, Bostjan ; MACKEIGAN, Jeffrey P ; YIN, Hongwei ; BROWN, Kevin M ; GIBBS, Richard ; TRENT, Jeffrey ; HAYWARD, Nicholas K ; BONAZZI, Vanessa F ; DUTTON-REGESTER, Ken ; AOUDE, Lauren G ; CHOW, Donald ; SEREDUK, Chris ; NIEMI, Natalie M ; TANG, Nanyun

Nature genetics, 2012-02, Vol.44 (2), p.165-169 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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5
Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma
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Artigo
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Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma

Bonazzi, Vanessa F ; Nancarrow, Derek J ; Stark, Mitchell S ; Moser, Ralf J ; Boyle, Glen M ; Aoude, Lauren G ; Schmidt, Christopher ; Hayward, Nicholas K Krahe, Ralf

PloS one, 2011-10, Vol.6 (10), p.e26121-e26121 [Periódico revisado por pares]

United States: Public Library of Science

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6
Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants
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Artigo
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Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants

Rayner, Jenna E ; Duffy, David L ; Smit, Darren J ; Jagirdar, Kasturee ; Lee, Katie J ; De'Ambrosis, Brian ; Smithers, B. Mark ; McMeniman, Erin K ; McInerney-Leo, Aideen M ; Schaider, Helmut ; Stark, Mitchell S ; Soyer, H. Peter ; Sturm, Richard A ; Prokunina-Olsson, Ludmila Prokunina-Olsson, Ludmila

PloS one, 2020-09, Vol.15 (9), p.e0238529-e0238529 [Periódico revisado por pares]

San Francisco: Public Library of Science

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7
Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor
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Artigo
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Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor

Boyle, Glen M. ; Woods, Susan L. ; Bonazzi, Vanessa F. ; Stark, Mitchell S. ; Hacker, Elke ; Aoude, Lauren G. ; Dutton-Regester, Ken ; Cook, Anthony L. ; Sturm, Richard A. ; Hayward, Nicholas K.

Pigment cell and melanoma research, 2011-06, Vol.24 (3), p.525-537 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Deficiencies in mismatch DNA repair: providing the soil for large-to-giant congenital melanocytic naevus development
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Artigo
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Deficiencies in mismatch DNA repair: providing the soil for large-to-giant congenital melanocytic naevus development

Stark, Mitchell S

British journal of dermatology (1951), 2023-01, Vol.188 (1), p.5-5 [Periódico revisado por pares]

England

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9
Defining the Molecular Genetics of Dermoscopic Naevus Patterns
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Artigo
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Defining the Molecular Genetics of Dermoscopic Naevus Patterns

Tan, Jean-Marie ; Tom, Lisa N. ; Soyer, H. Peter ; Stark, Mitchell S.

Dermatology (Basel), 2019-01, Vol.235 (1), p.19-34 [Periódico revisado por pares]

Basel, Switzerland

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10
Current Trends in Circulating Biomarkers for Melanoma Detection
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Artigo
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Current Trends in Circulating Biomarkers for Melanoma Detection

Huang, Nancy ; Lee, Katie J ; Stark, Mitchell S

Frontiers in medicine, 2022-04, Vol.9, p.873728-873728 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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