Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Miriam Verhoef-Post"'
Autor:
Ronny V. L. Joosen, Aat Vogelaar, Eric R. Coppoolse, Han de Rooij, Kent J. Bradford, Isabelle M. Henry, Leo Woudenberg, Luca Comai, Johan W. Schut, Heqiang Huo, Miriam Verhoef-Post
Publikováno v:
Huo, H; Henry, IM; Coppoolse, ER; Verhoef-Post, M; Schut, JW; de Rooij, H; et al.(2016). Rapid identification of lettuce seed germination mutants by bulked segregant analysis and whole genome sequencing. Plant Journal, 88(3), 345-360. doi: 10.1111/tpj.13267. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/54p0v49b
The Plant journal : for cell and molecular biology, vol 88, iss 3
The Plant journal : for cell and molecular biology, vol 88, iss 3
© 2016 The Authors The Plant Journal © 2016 John Wiley & Sons Ltd Lettuce (Lactuca sativa) seeds exhibit thermoinhibition, or failure to complete germination when imbibed at warm temperatures. Chemical mutagenesis was employed to develop lettuce li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8be77e02a6eb2c6940db561b02a92da1
http://www.escholarship.org/uc/item/54p0v49b
http://www.escholarship.org/uc/item/54p0v49b
Autor:
Axel P. N. Themmen, Annette Richter-Unruh, Stenvert L. S. Drop, Ada Funaro, Serge Lumbroso, Miriam Verhoef-Post, Auke Beishuizen, Leendert H. J. Looijenga, André van Marle, Annemieke M. Boot
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 96(7), E1197-E1205. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 96(7), E1197-E1205. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 96(7), E1197-E1205. Endocrine Society
Context: Germline and somatic activating mutations in the LH receptor (LHR) gene have been reported.Objective: Our objective was to perform mutation analysis of the LHR gene of patients with Leydig cell adenoma or hyperplasia. Functional studies were
Autor:
Leo J. Hofland, Bedette van de Zande, Miriam Verhoef-Post, Anke van Kerkwijk, A. J. van der Lely, Martin Huisman, Axel P. N. Themmen, Patric J.D. Delhanty, C. Gauna
Publikováno v:
American Journal of Physiology, Endocrinology and Metabolism, 299(3), E497-E505. American Physiological Society
Delhanty PJ, van Kerkwijk A, Huisman M, van de Zande B, Verhoef-Post M, Gauna C, Hofland L, Themmen AP, van der Lely AJ. Unsaturated fatty acids prevent desensitization of the human growth hormone secretagogue receptor by blocking its internalization
Publikováno v:
Journal of Biological Chemistry, 283(38), 25821-25828. American Society for Biochemistry and Molecular Biology Inc.
The luteinizing hormone (LH) receptor plays an essential role in male and female gonadal function. Together with the follicle-stimulating hormone (FSH) and thyroid stimulating hormone (TSH) receptors, the LH receptor forms the family of glycoprotein
Autor:
Steven W. J. Lamberts, Leo J. Hofland, Wouter W. de Herder, Axel P. N. Themmen, Richard A Feelders, Adrian J. L. Clark, Frank H. de Jong, Aart-Jan van der Lely, H. Jaap Bonjer, Miriam Verhoef-Post, Peter M. van Koetsveld
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 88, 230-237. Endocrine Society
In a substantial part of adrenal adenomas and hyperplasias from patients with Cushing's syndrome, cortisol production is controlled by the expression of aberrant hormone receptors on adrenocortical cells. We present in vivo and in vitro data of two p
Autor:
T.E. Romer, Miriam Verhoef-Post, Ch Sultan, Han G. Brunner, Annette Richter-Unruh, Axel P. N. Themmen, Maria Szarras-Czapnik, John W.M. Martens, Virginie Georget, Serge Lumbroso
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 87, 2506-13
Journal of Clinical Endocrinology and Metabolism, 87, 6, pp. 2506-13
Journal of Clinical Endocrinology and Metabolism, 87, 6, pp. 2506-13
Item does not contain fulltext Over the past 5 yr several inactivating mutations in the LH receptor gene have been demonstrated to cause Leydig cell hypoplasia, a rare autosomal recessive form of male pseudohermaphroditism. Here, we report the identi
Autor:
H. G. Brunner, Stenvert L. S. Drop, G. H. G. Sinnecker, Sergio P. A. Toledo, A. Richter-Unruh, W. A. Kors, H. T. Wessels, Axel P. N. Themmen, Miriam Verhoef-Post, John W.M. Martens, Annemie L.M. Boehmer
Publikováno v:
Clinical Endocrinology. 56:103-112
Summary background Defective male sex differentiation in patients with hypoplasia of Leydig cells (LCH) is caused by deficient LH receptor signal transduction. To further investigate the variety of LH receptor gene mutations present in LCH patients a
Autor:
Giuseppe Saggese, M.M.M. van Reen, H.A. Delemarre-Van de Waal, J. M. H. Buckler, A. P. N. Themmen, Hannie Kremer, W. Epping, H.G. Brunner, M. Pombo-Arias, George Moll, Stenvert L. S. Drop, John S. Parks, M. Jansen, Miriam Verhoef-Post, J.M. Wit, F. De Luca, H. A. Latif, B.J. Otten, John W.M. Martens, Edwin C. M. Mariman, N. Potau
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 84:1136-1140
Herein, we report mutation analysis of the LH receptor gene in 17 males with LH-independent precocious puberty, of which 8 were familial and 9 had a negative family history. A total of 7 different mutations (all previously reported) were detected in
Autor:
Jenny A. Visser, J. Anton Grootegoed, Anke McLuskey, Miriam Verhoef-Post, Piet Kramer, Axel P. N. Themmen
Publikováno v:
Endocrinology. 139:4244-4251
The clinical use of diethylstilbestrol (DES) by pregnant women has resulted in an increased incidence of genital carcinoma in the daugh- ters born from these pregnancies. Also, in the so-called DES-sons abnormalities were found, mainly, the presence
Autor:
Dirk G. de Rooij, Karin E. Slegtenhorst-Eegdeman, Miriam Verhoef-Post, J. Anton Grootegoed, Henk J. G. van de Kant, Cathy E. Bakker, Ben A. Oostra, Axel P. N. Themmen
Publikováno v:
Endocrinology. 139:156-162
The fragile X syndrome is the most frequent hereditary form of mental retardation. This X-linked disorder is, in most cases, caused by an unstable and expanding trinucleotide CGG repeat located in the 5′-untranslated region of the gene involved, th