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Piecing together the mosaic of rare skin diseases: an interview with Veronica Kinsler

Disease models & mechanisms, 2024-06, Vol.17 (6)

Kinsler, Veronica A

2024

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

PloS one, 2016-11, Vol.11 (11), p.e0166268-e0166268

2016

Volltextzugriff (PDF)

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

Journal of investigative dermatology, 2013-09, Vol.133 (9), p.2229-2236

2013

Volltextzugriff (PDF)

Response to “Guidance on screening MRI decisions for congenital melanocytic nevi”

Journal of the American Academy of Dermatology, 2024-03, Vol.90 (3), p.e109-e110

Kinsler, Veronica A.

2024

Volltextzugriff (PDF)

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

Journal of the American Academy of Dermatology, 2015-01, Vol.72 (1), p.108-114

2015

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Response to Torchia

Journal of investigative dermatology, 2023-12, Vol.143 (12), p.2537-2538

2023

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Segmental hemangioma of the head and neck: High prevalence of PHACE syndrome

Journal of the American Academy of Dermatology, 2017-02, Vol.76 (2), p.356-358

2017

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

Pigment cell and melanoma research, 2018-01, Vol.31 (1), p.95-109

2018

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

British journal of cancer, 2017-04, Vol.116 (8), p.990-993

2017

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Vitamin D status in children with congenital melanocytic nevi

Pediatric dermatology, 2024-01, Vol.41 (1), p.58-60

2024

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Inflammatory linear verrucous epidermal nevus should be genotyped to direct treatment and genetic counseling

Journal of the American Academy of Dermatology, 2024-06, Vol.90 (6), p.1279-1280

2024

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Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

The Journal of clinical investigation, 2018-04, Vol.128 (4), p.1496-1508

2018

Volltextzugriff (PDF)

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

Journal of investigative dermatology, 2015-11, Vol.135 (11), p.2902-2902

2015

Volltextzugriff (PDF)

The GA4GH Phenopacket schema defines a computable representation of clinical data

Nature biotechnology, 2022-06, Vol.40 (6), p.817-820

2022

Volltextzugriff (PDF)

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause

Nature genetics, 2021-09, Vol.53 (9), p.1360-1372

2021

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Impact of public exhibition on the perception of birthmarks

Pediatric dermatology, 2023-07, Vol.40 (4), p.615-620

2023

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

Journal of investigative dermatology, 2016-04, Vol.136 (4), p.770-778

2016

Volltextzugriff (PDF)

GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses

Journal of investigative dermatology, 2020-05, Vol.140 (5), p.1110-1113

2020

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In Memoriam : Prof. John I. Harper MB BS MD FRCP FRCPCH 1950‐2021

Pediatric dermatology, 2021-07, Vol.38 (4), p.757-758

2021

Volltextzugriff (PDF)

GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics

Journal of investigative dermatology, 2024-04, Vol.144 (4), p.811-819.e4

2024

Volltextzugriff (PDF)

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

Journal of the American Academy of Dermatology, 2020-12, Vol.83 (6), p.1779-1781

2020

Volltextzugriff (PDF)

RNA Therapy for Oncogenic NRAS-Driven Nevi Induces Apoptosis

Journal of investigative dermatology, 2024-06

2024

Volltextzugriff (PDF)

Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway Inhibition

Journal of investigative dermatology, 2024-03, Vol.144 (3), p.593-600.e7

2024

Volltextzugriff (PDF)

Somatic activating mutations in Pik3ca cause sporadic venous malformations in mice and humans

Science translational medicine, 2016-03, Vol.8 (332), p.332ra43

2016

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Piecing together the mosaic of rare skin diseases: an interview with Veronica Kinsler

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

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

Response to “Guidance on screening MRI decisions for congenital melanocytic nevi”

Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

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

Response to Torchia

Segmental hemangioma of the head and neck: High prevalence of PHACE syndrome

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

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

Vitamin D status in children with congenital melanocytic nevi

Inflammatory linear verrucous epidermal nevus should be genotyped to direct treatment and genetic counseling

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

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

The GA4GH Phenopacket schema defines a computable representation of clinical data

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause

Impact of public exhibition on the perception of birthmarks

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

GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses

In Memoriam : Prof. John I. Harper MB BS MD FRCP FRCPCH 1950‐2021

GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics

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

RNA Therapy for Oncogenic NRAS-Driven Nevi Induces Apoptosis

Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway Inhibition

Somatic activating mutations in Pik3ca cause sporadic venous malformations in mice and humans

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