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11. Mechanical stress regulates bone regulatory gene expression independent of estrogen and vitamin D deficiency in rats. Issue 1 (21st July 2020)

12. Pathogenic effect of a TGFBR1 mutation in a family with Loeys–Dietz syndrome. Issue 10 (1st September 2019)

13. Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome. Issue 1 (13th December 2011)

14. Primary ciliary dyskinesia in Volendam: Diagnostic and phenotypic features in patients with a CCDC114 mutation. Issue 1 (27th March 2022)

15. Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome. Issue 22 (3rd May 2017)

16. RNA Sequencing of Creatine Transporter (SLC6A8) Deficient Fibroblasts Reveals Impairment of the Extracellular Matrix. Issue 9 (15th July 2014)

17. SMAD2 Mutations Are Associated with Arterial Aneurysms and Dissections. Issue 12 (10th September 2015)

18. The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1. Issue 8 (17th June 2019)

19. Transdifferentiation of Human Dermal Fibroblasts to Smooth Muscle‐Like Cells to Study the Effect of MYH11 and ACTA2 Mutations in Aortic Aneurysms. Issue 4 (27th January 2017)