Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Miriam Hulsbeek"'
Autor:
Miriam Hulsbeek, Andy C.-M. Chang, Jackie B.M. Janosi, Debora de Jong, Jane R. Noble, Katherine J. Jeffrey, Roger R. Reddel
Publikováno v:
Molecular and Cellular Endocrinology. 112:241-247
Stanniocalcin is a glycoprotein hormone previously considered present only in bony fish where it is secreted by the corpuscles of Stannius, endocrine organs involved in Ca2+ homeostasis. In fish, stanniocalcin was thought to be an adaptation for Ca2+
Autor:
Gyula Kovacs, Anneke Y. van der Veen, Anke van den Berg, Charles H.C.M. Buys, Miriam Hulsbeek, Robert M. Gemmill, Harry A. Drabkin
Publikováno v:
Genes, Chromosomes and Cancer. 12:224-228
In a family with a constitutional translocation t(3;6), the oldest member carrying the translocation had developed multiple nonpapillary renal cell carcinomas (RCCs). The translocation breakpoint was positioned between 3p13 and 3p14.1. This is close
Autor:
Saskia Vliex, Connie R. Bezzina, Miriam Hulsbeek, Mehran Firouzi, Lodewijk Sandkuijl, Habo J. Jongsma, Irene M. van Langen, Martin B. Rook, W. Antoinette Groenewegen, Arthur A.M. Wilde, Jeroen P.P. Smits
Publikováno v:
Circulation research, 92(1), 14-22. LIPPINCOTT WILLIAMS & WILKINS
Circulation research, 92(1), 14-22. Lippincott Williams and Wilkins
Circulation research, 92(1), 14-22. Lippincott Williams and Wilkins
Atrial standstill (AS) is a rare arrhythmia that occasionally appears to be genetically determined. This study investigates the genetic background of this arrhythmogenic disorder in a large family. Forty-four family members were clinically evaluated.
Autor:
Maartje Boon, Cees P. Zwanikken, Robert M.W. Hofstra, Charles H.C.M. Buys, Jacques De Keyser, Gerard J. te Meerman, Peter Terpstra, Geert T. Spijker, Miriam Hulsbeek, John Raelson, Marcel Bruinenberg, Ilja M. Nolte
Publikováno v:
Neurogenetics. 3(4)
Multiple sclerosis (MS) is a complex disease that is partly genetic in origin. Although an association of MS with specific human leukocyte antigen (HLA) types has been known for almost 30 years, the nature of this relationship has remained unclear. F
Autor:
P A Crossey, Frances M. Richards, Amanda Prowse, Eamonn R. Maher, Charles H.C.M. Buys, Miriam Hulsbeek, Keith Foster, Anke van den Berg, Malcolm A. Ferguson-Smith, Paul Cairns, Nabeel A. Affara, Stewart Fleming
Publikováno v:
Human molecular genetics. 3(12)
Loss of heterozygosity (LOH) studies have suggested that somatic mutations of a tumour suppressor gene or genes on chromosome 3p are a critical event in the pathogenesis of non-familial renal cell carcinoma (RCC). Germline mutations of the von Hippel
Publikováno v:
Cancer Genetics and Cytogenetics. 91:139
Autor:
Patrick M.J.F. Veldhuis, Anneke Y. van der Veen, Anke van den Berg, Klaas Kok, Susan L. Naylor, Charles H.C.M. Buys, Miriam Hulsbeek
Publikováno v:
Cancer Genetics and Cytogenetics. 77:187
Autor:
Miriam Hulsbeek, Harry A. Drabkin, S Storkel, Anke van den Berg, Charles H.C.M. Buys, Debora de Jong
Publikováno v:
Cancer Genetics and Cytogenetics. 77:191
Autor:
Gyula Kovacs, Charles H.C.M. Buys, Anneke Y. van der Veen, Anke van den Berg, Miriam Hulsbeek, Klaas Kok, Harry A. Drabkin
Publikováno v:
Cancer Genetics and Cytogenetics. 77:176