Satellite Lesions in Congenital Melanocytic Nevi—Time for a Change of Name

por KINSLER, VERONICA
Publicado 2011

The patterns of birthmarks suggest a novel population of melanocyte precursors arising around the time of gastrulation

por Kinsler, Veronica A., Larue, Lionel
Publicado 2017

Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold – A Potential Therapeutic Intervention for Skin Diseases

por Chen, Wenjie, Kinsler, Veronica A., Macmillan, Derek, Di, Wei-Li
Publicado 2016

MEK inhibition appears to improve symptom control in primary NRAS-driven CNS melanoma in children

por Kinsler, Veronica A, O'Hare, Patricia, Jacques, Thomas, Hargrave, Darren, Slater, Olga
Publicado 2017

The adverse effect profile of acitretin in a pediatric dermatology population—Longitudinal cohort study and recommendations for monitoring

por Cave, Anna, Plumptre, Isabella, Mellerio, Jemima E., Martinez, Anna E., Kinsler, Veronica A.
Publicado 2020

The adverse effect profile of oral azathioprine in pediatric atopic dermatitis, and recommendations for monitoring

por Fuggle, Nicholas R., Bragoli, Walter, Mahto, Anjali, Glover, Mary, Martinez, Anna E., Kinsler, Veronica A.
Publicado 2015

Copy number abnormalities in new or progressive ‘neurocutaneous melanosis’ confirm it to be primary CNS melanoma

por Kinsler, Veronica A., Polubothu, Satyamanaasa, Calonje, J. Eduardo, Chong, W. Kling, Thompson, Dominic, Jacques, Thomas S., Morrogh, Deborah
Publicado 2016

Widespread dynamic and pleiotropic expression of the melanocortin‐1‐receptor (MC1R) system is conserved across chick, mouse and human embryonic development

por Thomas, Anna C., Heux, Pauline, Santos, Chloe, Arulvasan, Wisenave, Solanky, Nita, Carey, Magalie E., Gerrelli, Dianne, Kinsler, Veronica A., Etchevers, Heather C.
Publicado 2018

Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI

por Kinsler, Veronica A., Paine, Simon M. L., Anderson, Glenn W., Wijesekara, D. Saraji, Sebire, Neil J., Chong, Wui K., Harkness, William, Aylett, Sarah E., Jacques, Thomas S.
Publicado 2012

Next-Generation Sequencing of Nevus Spilus–Type Congenital Melanocytic Nevus: Exquisite Genotype–Phenotype Correlation in Mosaic RASopathies

por Kinsler, Veronica A, Krengel, Sven, Riviere, Jean-Baptiste, Waelchli, Regula, Chapusot, Carolina, Al-Olabi, Lara, Faivre, Laurence, Haenssle, Holger A, Weibel, Lisa, Jeudy, Géraldine, Vabres, Pierre
Publicado 2014

Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

por Kinsler, Veronica A, Abu-Amero, Sayeda, Budd, Peter, Jackson, Ian J, Ring, Susan M, Northstone, Kate, Atherton, David J, Bulstrode, Neil W, Stanier, Philip, Hennekam, Raoul C, Sebire, Neil J, Moore, Gudrun E, Healy, Eugene
Publicado 2012

Molecular Genetic Dissection of Inflammatory Linear Verrucous Epidermal Naevus Leads to Successful Targeted Therapy

por Riachi, Melissa, Polubothu, Satyamaanasa, Stadnik, Paulina, Hughes, Connor, Martin, Sara Barberan, Charman, Carolyn R., Cheng, Iek Leng, Gholam, Karolina, Ogunbiyi, Olumide, Paige, David G., Sebire, Neil J., Pittman, Alan, Di, Wei-Li, Kinsler, Veronica A.
Publicado 2021

Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita

por Tummala, Hemanth, Walne, Amanda, Buccafusca, Roberto, Alnajar, Jenna, Szabo, Anita, Robinson, Peter, McConkie-Rosell, Allyn, Wilson, Meredith, Crowley, Suzanne, Kinsler, Veronica, Ewins, Anna-Maria, Madapura, Pradeepa M., Patel, Manthan, Pontikos, Nikolas, Codd, Veryan, Vulliamy, Tom, Dokal, Inderjeet
Publicado 2022

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

por Kinsler, Veronica A, Thomas, Anna C, Ishida, Miho, Bulstrode, Neil W, Loughlin, Sam, Hing, Sandra, Chalker, Jane, McKenzie, Kathryn, Abu-Amero, Sayeda, Slater, Olga, Chanudet, Estelle, Palmer, Rodger, Morrogh, Deborah, Stanier, Philip, Healy, Eugene, Sebire, Neil J, Moore, Gudrun E
Publicado 2013

Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling

por Pawlikowski, Jeffrey S, Brock, Claire, Chen, Sheau-Chiann, Al-Olabi, Lara, Nixon, Colin, McGregor, Fiona, Paine, Simon, Chanudet, Estelle, Lambie, Wendy, Holmes, William M, Mullin, James M, Richmond, Ann, Wu, Hong, Blyth, Karen, King, Ayala, Kinsler, Veronica A, Adams, Peter D
Publicado 2015

Senescent cells evade immune clearance via HLA-E-mediated NK and CD8(+) T cell inhibition

por Pereira, Branca I., Devine, Oliver P., Vukmanovic-Stejic, Milica, Chambers, Emma S., Subramanian, Priya, Patel, Neil, Virasami, Alex, Sebire, Neil J., Kinsler, Veronica, Valdovinos, Alexis, LeSaux, Claude Jourdan, Passos, João F., Antoniou, Antony, Rustin, Malcom H. A., Campisi, Judith, Akbar, Arne N.
Publicado 2019

GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis

por Sliepka, Joseph M., McGriff, Sarah C., Rossetti, Linda Z., Bizargity, Peyman, Streff, Haley, Lee, Yi-Shan, Dai, Hongzheng, Polubothu, Satyamaanasa, Lee, Grace, Ren, Vicky, Hunter, Jill V., Curry, Daniel J., Scaglia, Fernando, Adesina, Adekunle M., Ali, Irfan, Kinsler, Veronica, Burrage, Lindsay C., Marafi, Dana
Publicado 2019

SAT-224 Recurrent Co-Driver Mutation in CTNNB1-Mutant Aldosterone-producing Adenomas (APA), Causing Reversible Hypertension in Puberty, Pregnancy or Menopause

por Zhou, Junhua, Cabrera, Claudia P, Azizan, Elena A B, Fernandes-Rosa, Fabio, Cottrell, Emily, Amar, Laurence, Argentesi, Giulia, Wu, Xilin, Marker, Alison, Jordan, Suzanne, Polubothu, Satyamaanasa, Berney, Daniel M, Tuthill, Antoinette, Karet, Fiona E, Metherell, Louise, Teo, Ada, Thakker, Rajesh V, Drake, William, Boulkroun, Sheerazed, Kinsler, Veronica, Storr, Helen Louise, Zennaro, Maria-Christina, Brown, Morris Jonathan
Publicado 2020

Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes

por Lescai, Francesco, Bonfiglio, Silvia, Bacchelli, Chiara, Chanudet, Estelle, Waters, Aoife, Sisodiya, Sanjay M., Kasperavičiūtė, Dalia, Williams, Julie, Harold, Denise, Hardy, John, Kleta, Robert, Cirak, Sebahattin, Williams, Richard, Achermann, John C., Anderson, John, Kelsell, David, Vulliamy, Tom, Houlden, Henry, Wood, Nicholas, Sheerin, Una, Tonini, Gian Paolo, Mackay, Donna, Hussain, Khalid, Sowden, Jane, Kinsler, Veronica, Osinska, Justyna, Brooks, Tony, Hubank, Mike, Beales, Philip, Stupka, Elia
Publicado 2012

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

por Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan, Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien, Bourrat, Emmanuelle, Chiaverini, Christine, Chong, W. Kling, Duffourd, Yannis, Glover, Mary, Groesser, Leopold, Hadj-Rabia, Smail, Hamm, Henning, Happle, Rudolf, Mushtaq, Imran, Lacour, Jean-Philippe, Waelchli, Regula, Wobser, Marion, Vabres, Pierre, Patton, E. Elizabeth, Kinsler, Veronica A.
Publicado 2016