T. Sepp

发表

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.

S Povey, D Ravine, D Lindhout, 1997, Science.

Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokers.

D. Clayton, A. Bird, A. Moore, 2006, Investigative ophthalmology & visual science.

Mutations in the TSC1 gene account for a minority of patients with tuberous sclerosis.

A. Green, T. Sepp, J. Ali, 1998, Journal of medical genetics.

Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysis.

A. Green, T. Sepp, J. Yates, 1997, Human molecular genetics.

Mutations in the TSC 1 gene account for a minority of patients with tuberous sclerosis

T. Sepp, S. Ward, J. Yates, 2022 .

“The Narrative is Ambiguous and that Location Isn’t the Right Location”: Presenting and Interpreting Medieval Saints Today in Canterbury, Durham and York

T. Sepp, 2019, Journal of Ethnology and Folkloristics.

Caminoisation and Cathedrals: replication, the heritagisation of religion, and the spiritualisation of heritage

T. Sepp, Marion Bowman, 2018, Religion.

Mutations in the TSC2 gene: analysis of the complete coding sequence using the protein truncation test (PTT).

A. Green, T. Sepp, S. Ward, 1997, Human molecular genetics.

Complement C3 variant and the risk of age-related macular degeneration.

I. Deary, D. Clayton, A. Bird, 2007, The New England journal of medicine.

Journey in a Life Story and Pilgrimage: Exploring the Connection Between Humans and Place in a First-Person Narrative

T. Sepp, T. Jaago, 2021, Journal of Ethnology and Folkloristics.

Cathedrals, Community, and Identity

T. Sepp, John Jenkins, 2020 .

The Pilgrimage Landscape in Contemporary Estonia: New Routes, Narratives, and Re-Christianization

T. Sepp, Atko Remmel, 2020 .

A Cathedral Is Not Just for Christmas:

T. Sepp, S. Coleman, Marion Bowman, 2019, The Public Work of Christmas.

Visibly different

T. Sepp, S. Coleman, Marion Bowman, 2018, The Desecularisation of the City.

Investigations of virus-protozoa relationships in the model of the free-living ciliate Tetrahymena pyriformis and adenovirus type 3.

T. Sepp, L. Järvekülg, M. Saarma, 1992, European journal of protistology.

Loss of heterozygosity in tuberous sclerosis hamartomas.

T. Sepp, A. Green, J. Yates, 1996, Journal of medical genetics.

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.

G. Abecasis, L. Smeeth, D. Weeks, 2012, International journal of epidemiology.

Clonality of tuberous sclerosis harmatomas shown by non-random X-chromosome inactivation

A. Green, T. Sepp, J. Yates, 1996, Human Genetics.

Complement C 3 Variant and the Risk of Age-Related Macular Degeneration

I. Deary, D. Clayton, A. Bird, 2007 .

An EcoRV polymorphism in exon 40 of the tuberous sclerosis 2 (TSC2) gene.

A. Green, T. Sepp, J. Yates, 1997, Molecular and cellular probes.

Complement Factor H Variant Y 402 H Is a Major Risk Determinant for Geographic Atrophy and Choroidal Neovascularization in Smokers and Nonsmokers

D. Clayton, A. Bird, A. Moore, 2006 .

D. Clayton, S. Harding, C. Bunce, 2011, British Journal of Ophthalmology.

Hamartomas from patients with tuberous sclerosis show loss of heterozygosity for chromosome 9q34

A. Green, T. Sepp, J. Yates, 1994 .

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.

G. Abecasis, L. Smeeth, D. Weeks, 2012, International journal of epidemiology.

Quantification of SCH 39166, a novel selective D1 dopamine receptor in rat brain and blood antagonist,

J. Hietala, T. Sepp, J. Lappalainen, 1992 .