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  1. No Access

    Article

    Changes in white adipose tissue gene expression in a randomized control trial of dieting obese men with lowered serum testosterone alone or in combination with testosterone treatment

    The aim of this study was to determine early weight loss-associated changes in subcutaneous abdominal white adipose tissue (WAT) gene expression in obese men with lowered serum testosterone by RNA next-generat...

    Mathis Grossmann, Mark Ng Tang Fui, Tian Nie, Rudolf Hoermann… in Endocrine (2021)

  2. No Access

    Article

    A body shape index (ABSI) reflects body composition changes in response to testosterone treatment in obese men

    Interventions such as testosterone treatment may change body composition and metabolic outcomes without substantial changes in weight and BMI.

    Rudolf Hoermann, Mark Ng Tang Fui, Jesse C. Krakauer… in International Journal of Obesity (2019)

  3. Article

    Open Access

    Effect of testosterone treatment on bone remodelling markers and mineral density in obese dieting men in a randomized clinical trial

    To assess the effect of testosterone treatment on bone remodelling and density in dieting obese men, 100 obese men aged 53 years (interquartile range 47–60) with a total testosterone level <12 nmol/L receiving...

    Mark Ng Tang Fui, Rudolf Hoermann, Brendan Nolan, Michelle Clarke… in Scientific Reports (2018)

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  4. Article

    Open Access

    Effects of testosterone treatment on body fat and lean mass in obese men on a hypocaloric diet: a randomised controlled trial

    Whether testosterone treatment has benefits on body composition over and above caloric restriction in men is unknown. We hypothesised that testosterone treatment augments diet-induced loss of fat mass and prev...

    Mark Ng Tang Fui, Luke A. Prendergast, Philippe Dupuis, Manjri Raval… in BMC Medicine (2016)

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  5. No Access

    Article

    A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma

    Congenital polycythemias have diverse etiologies, including mutations in the hypoxia sensing pathway. These include HIF2A at exon 12, VHL gene (Chuvash polycythemia), and PHD2 mutations, which in one family was a...

    Felipe R. Lorenzo, Chunzhang Yang, Mark Ng Tang Fui… in Journal of Molecular Medicine (2013)

  6. No Access

    Chapter

    Kennedy’s Disease

    Kennedy’ s disease (KD) or spinobulbar muscular atrophy is a hereditary X-linked, progressive neurodegenerative condition caused by an expansion of the CAG triplet repeat in the first exon of the androgen rece...

    Jeffrey D. Zajac, Mark Ng Tang Fui in Tandem Repeat Polymorphisms (2012)