Publications by authors named "Thilini Gamage"

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Unraveling Sociocultural Influences on Leptospirosis Incidence and Prevalence: A Qualitative Study in Sri Lanka.
Samitha Udayanga, Dinesha Kankanamge, Thilini Gamage, Lahiru Suresh De Zoysa, Yasasi Chamathya

Asia Pac J Public Health· September 2024

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A single amino acid deletion in the ER Ca sensor STIM1 reverses the in vitro and in vivo effects of the Stormorken syndrome-causing R304W mutation.
Thilini H Gamage, Herwig Grabmayr, Ferdinand Horvath, Marc Fahrner, Doriana Misceo

Sci Signal· February 2023

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A girl with a neurodevelopmental syndrome, adducted thumbs and frequent infections caused by novel homozygous variant in DEAF1.
Dulika S Sumathipala, Doriana Misceo, Selma Mujezinovic Larsen, Tuva Barøy, Thilini H Gamage

Clin Dysmorphol· April 2020

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STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone.
Thilini H Gamage, Emma Lengle, Gjermund Gunnes, Helen Pullisaar, Asbjørn Holmgren

Cell Calcium· January 2020

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STIM1 R304W causes muscle degeneration and impaired platelet activation in mice.
Thilini H Gamage, Gjermund Gunnes, Robert Hugh Lee, William Edward Louch, Asbjørn Holmgren

Cell Calcium· December 2018

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BCL2-modifying factor promotes germ cell loss during murine oogenesis.
Kavitha Vaithiyanathan, Seng H Liew, Nadeen Zerafa, Thilini Gamage, Michele Cook

Reproduction· May 2016

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Localisation of the Notch family in the human endometrium of fertile and infertile women.
Michelle Van Sinderen, Carly Cuman, Thilini Gamage, Katarzyna Rainczuk, Tiki Osianlis

J Mol Histol· December 2014

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PUMA regulates germ cell loss and primordial follicle endowment in mice.
Michelle Myers, F Hamish Morgan, Seng H Liew, Nadeen Zerafa, Thilini Upeksha Gamage

Reproduction· August 2014

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A balanced de novo inv(7)(p14.3q22.3) disrupting PDE1C and ATXN7L1 in a 14-year old developmentally delayed boy.
Thilini H Gamage, Doriana Misceo, Madeleine Fannemel, Eirik Frengen

Eur J Med Genet· July 2013

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An infant born to a mother with gestational diabetes presenting with 49,XXXXY syndrome and renal agenesis-a case report.
Dulika Sumathipala, Thilini Gamage, Bandula Wijesiriwardena, Rohan W Jayasekara, Vajira H W Dissanayake

J Clin Res Pediatr Endocrinol· December 2012

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A child with mosaicism for deletion (14)(q11.2q13).
Thilini H Gamage, Imaya U H Godapitiya, Shakila Nanayakkara, Rohan W Jayasekara, Vajira H W Dissanayake

Indian J Hum Genet· January 2012

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