Lista de obras - N Rajan - Dominio Público Uruguay

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.

artículo científico publicado en 2013

A novel link between keratoderma and cardiomyopathy: contiguous gene deletion involving the desmoglein gene cluster

artículo científico publicado en 2017

A tale of two sisters: identical IL36RN mutations and discordant phenotypes.

artículo científico publicado en 2015

Basal cell carcinoma arising in association with trichoepithelioma in a case of Brooke‐Spiegler syndrome with a novel genetic mutation in CYLD ⬇️

artículo científico publicado el 9 de agosto de 2012

Basaloid follicular proliferations, brain tumours and SUFU

artículo científico publicado en 2020

CYLD GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas

artículo científico publicado en 2015

CYLD in health and disease

artículo científico publicado en 2023

Clinical outcomes and response of patients applying topical therapy for pyoderma gangrenosum: A prospective cohort study

artículo científico publicado en 2016

Cutaneous immune-related adverse events in patients with melanoma treated with checkpoint inhibitors

scientific article published on 04 January 2021

Cutaneous xanthomatosis: a novel presentation of hypercholesterolaemia in primary sclerosing cholangitis

scientific article published on 01 July 2006

Demonstration of gastrointestinal venous malformations in blue rubber bleb naevus syndrome using capsule endoscopy.

artículo científico publicado en 2008

Development and validation of LC-MS/MS with in-source collision-induced dissociation for the quantification of pegcantratinib in human skin tumors

artículo científico publicado en 2017

Diverse assays from a single skin punch biopsy to assess topical drug intervention

artículo científico publicado en 2019

Dry skin and blistering in childhood.

artículo científico publicado en 2016

Dysregulated TRK signalling is a therapeutic target in CYLD defective tumours

artículo científico

Enucleation of cylindromas in Brooke-Spiegler syndrome: a novel surgical technique ⬇️

artículo científico publicado en 2014

Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families

artículo científico publicado en 2009

Human cowpox: presentation and investigation in an era of bioterrorism

scientific article published on 01 October 2005

Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1

artículo científico publicado en 2021

Idiopathic infantile pyoderma gangrenosum with stridor responsive to infliximab

artículo científico publicado en 2009

Impetiginized eczema arising within a port-wine stain of the arm

artículo científico publicado en 2006

Infiltrative recurrent eccrine spiradenoma of the anterior neck treated using Mohs micrographic surgery.

artículo científico publicado en 2013

Inherited pulmonary cylindromas: extending the phenotype of CYLD mutation carriers

artículo científico publicado en 2018

Inherited skin tumour syndromes

artículo científico publicado en 2017

Mesenteric cysts in naevoid basal cell carcinoma syndrome: a mimic of metastatic disease.

artículo científico publicado en 2015

Milia: a useful clinical marker of CYLD mutation carrier status

artículo científico publicado en 2017

Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutation

artículo científico

Multiple Facial Trichoepitheliomas and Vulval Cysts: Extending the Phenotypic Spectrum in CYLD Cutaneous Syndrome.

artículo científico publicado en 2017

Overexpression of MYB drives proliferation of CYLD-defective cylindroma cells

artículo científico publicado en 2016

Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation ⬇️

artículo científico publicado en 2017

Pre-emptive intra-auricular electrosurgical resurfacing of cylindromas to prevent conductive deafness in CYLD cutaneous syndrome

scientific article published on 27 July 2020

Public engagement lectures targeting prospective medical students: an opportunity for dermatology

artículo científico publicado en 2018

Reading through genetic 'stop signs': a therapeutic strategy in genetic skin disease

artículo científico publicado en 2020

Squamous cell carcinoma arising within a facial port-wine stain treated by mohs micrographic surgical excision

scientific article published on 01 June 2006

Squamous cell carcinomas in linear epidermal naevi

scientific article published on 28 June 2018

The cylindromatosis gene product, CYLD, interacts with MIB2 to regulate notch signalling

artículo científico publicado en 2014

The punch and graft technique: a novel method of surgical treatment for chondrodermatitis nodularis helicis.

artículo científico publicado en 2007

Transcriptomic profiling of human skin biopsies in the clinical trial setting: A protocol for high quality RNA extraction from skin tumours.

artículo científico publicado en 2018

Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expression

artículo científico publicado en 2011

Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours: study protocol for a randomised controlled trial

artículo científico publicado en 2017

Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction

artículo científico publicado en 2009

Understanding Inherited Cylindromas: Clinical Implications of Gene Discovery

artículo científico publicado en 2017

p63 and smooth muscle actin expression in low-grade spiradenocarcinomas in a case of CYLD cutaneous syndrome

artículo científico publicado en 2018

Lista de obras de N Rajan

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.

A novel link between keratoderma and cardiomyopathy: contiguous gene deletion involving the desmoglein gene cluster

A tale of two sisters: identical IL36RN mutations and discordant phenotypes.

Basal cell carcinoma arising in association with trichoepithelioma in a case of Brooke‐Spiegler syndrome with a novel genetic mutation in CYLD ⬇️

Basaloid follicular proliferations, brain tumours and SUFU

CYLD GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas

CYLD in health and disease

Clinical outcomes and response of patients applying topical therapy for pyoderma gangrenosum: A prospective cohort study

Cutaneous immune-related adverse events in patients with melanoma treated with checkpoint inhibitors

Cutaneous xanthomatosis: a novel presentation of hypercholesterolaemia in primary sclerosing cholangitis

Demonstration of gastrointestinal venous malformations in blue rubber bleb naevus syndrome using capsule endoscopy.

Development and validation of LC-MS/MS with in-source collision-induced dissociation for the quantification of pegcantratinib in human skin tumors

Diverse assays from a single skin punch biopsy to assess topical drug intervention

Dry skin and blistering in childhood.

Dysregulated TRK signalling is a therapeutic target in CYLD defective tumours

Enucleation of cylindromas in Brooke-Spiegler syndrome: a novel surgical technique ⬇️

Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families

Human cowpox: presentation and investigation in an era of bioterrorism

Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1

Idiopathic infantile pyoderma gangrenosum with stridor responsive to infliximab

Impetiginized eczema arising within a port-wine stain of the arm

Infiltrative recurrent eccrine spiradenoma of the anterior neck treated using Mohs micrographic surgery.

Inherited pulmonary cylindromas: extending the phenotype of CYLD mutation carriers

Inherited skin tumour syndromes

Mesenteric cysts in naevoid basal cell carcinoma syndrome: a mimic of metastatic disease.

Milia: a useful clinical marker of CYLD mutation carrier status

Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutation

Multiple Facial Trichoepitheliomas and Vulval Cysts: Extending the Phenotypic Spectrum in CYLD Cutaneous Syndrome.

Overexpression of MYB drives proliferation of CYLD-defective cylindroma cells

Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation ⬇️

Pre-emptive intra-auricular electrosurgical resurfacing of cylindromas to prevent conductive deafness in CYLD cutaneous syndrome

Public engagement lectures targeting prospective medical students: an opportunity for dermatology

Reading through genetic 'stop signs': a therapeutic strategy in genetic skin disease

Squamous cell carcinoma arising within a facial port-wine stain treated by mohs micrographic surgical excision

Squamous cell carcinomas in linear epidermal naevi

The cylindromatosis gene product, CYLD, interacts with MIB2 to regulate notch signalling

The punch and graft technique: a novel method of surgical treatment for chondrodermatitis nodularis helicis.

Transcriptomic profiling of human skin biopsies in the clinical trial setting: A protocol for high quality RNA extraction from skin tumours.

Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expression

Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours: study protocol for a randomised controlled trial

Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction

Understanding Inherited Cylindromas: Clinical Implications of Gene Discovery

p63 and smooth muscle actin expression in low-grade spiradenocarcinomas in a case of CYLD cutaneous syndrome