S. Sikkink

发表

X-linked retinoschisis: an update

P. Stanga, N. Parry, D. Trump, 2006, Journal of Medical Genetics.

Age-related changes in female scalp dermal sheath and dermal fibroblasts: how the hair follicle environment impacts hair ageing.

A. Pawlus, M. Thornton, G. Westgate, 2020, The Journal of investigative dermatology.

Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp

D. Tobin, S. Mine, O. Freis, 2020, Scientific Reports.

Basal cell carcinomas and squamous cell carcinomas of human skin show distinct patterns of chromosome loss.

J. Rees, A. Quinn, S. Sikkink, 1994, Cancer research.

The genetics of frontotemporal lobar degeneration

S. Rollinson, S. Pickering-Brown, S. Sikkink, 2007, Current opinion in neurology.

Deletion mapping of chromosome 3p and 13q and preliminary analysis of the FHIT gene in human nonmelanoma skin cancer.

J. Rees, I. Rehman, S. Sikkink, 1997, The Journal of investigative dermatology.

Infrequent mutation of p16INK4 in sporadic melanoma.

E. Healy, J. Rees, S. Sikkink, 1996, The Journal of investigative dermatology.

Lysophosphatidic Acid Promotes Cell Migration through STIM1- and Orai1-Mediated Ca2+i Mobilization and NFAT2 Activation

N. Reynolds, K. Ross, Darren L. Johnson, 2012, The Journal of investigative dermatology.

In vitro and ex vivo examination of topical Pomiferin treatments.

D. Tobin, J. V. Gruber, S. Sikkink, 2014, Fitoterapia.

E‐cadherin mediates ultraviolet radiation‐ and calcium‐induced melanin transfer in human skin cells

D. Tobin, S. Singh, R. Kurfurst, 2017, Experimental dermatology.

E-Cadherin mediates UVR-and calcium-induced melanin transfer in human skin cells

D. Tobin, S. Singh, R. Kurfurst, 2017 .

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma.

I. Jackson, A. Carothers, E. Healy, 1996, Human molecular genetics.

TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

D. Neary, D. Mann, M. Esiri, 2011, Acta Neuropathologica.

Delineation of two distinct deleted regions on chromosome 9 in human non‐melanoma skin cancers

J. Rees, A. Quinn, S. Sikkink, 1994, Genes, chromosomes & cancer.

Microsatellite instability in human non-melanoma and melanoma skin cancer.

E. Healy, J. Rees, A. Quinn, 1995, The Journal of investigative dermatology.

Explorer The Asp 84 Glu variant of the melanocortin 1 receptor ( MC 1 R ) is associated with melanoma

I. Jackson, A. Carothers, J. Rees, 2015 .

Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy

E. Bigio, D. Mann, H. Akiyama, 2010, Acta Neuropathologica.

Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease

D. Mann, H. Akiyama, M. Hasegawa, 2010, Acta Neuropathologica.

TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing

D. Neary, D. Mann, A. Lees, 2009, Acta Neuropathologica.

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

D. Neary, M. Rossor, N. Cairns, 2009, Neurobiology of Aging.

Rapid communication Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

D. Neary, M. Rossor, N. Cairns, 2009 .