Christoffer Löf

Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort

Christoffer Löf, Konrad Patyra, Teemu Kuulasmaa et al. · Thyroid · 2016 · 79 citations · Full text

Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

Hakan Cangül, Xiao-Hui Liao, Erik Schoenmakers et al. · JCI Insight · 2018 · 73 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +16

Transient Receptor Potential Canonical 1 (TRPC1) Channels as Regulators of Sphingolipid and VEGF Receptor Expression

Muhammad Yasir Asghar, Melissa Magnusson, Kati Kemppainen et al. · Journal of Biological Chemistry · 2015 · 58 citations · Full text

Signal Transduction, Molecular Physiology, Signaling Pathway +11

An autocrine sphingosine-1-phosphate signaling loop enhances NF-κB-activation and survival

Tomas Blom, Nina Bergelin, Annika Meinander et al. · BMC Cell Biology · 2010 · 46 citations · Full text

Sphingosine Kinase as an Oncogene: Autocrine Sphingosine 1-Phoshate Modulates ML-1 Thyroid Carcinoma Cell Migration by a Mechanism Dependent on Protein Kinase C-α and ERK1/2

Nina Bergelin, Tomas Blom, Jari Heikkilä et al. · Endocrinology · 2008 · 45 citations · Full text