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There are 16868 results for: content related to: Robustness of the hypoxic response: Another job for miRNAs?

  1. GENETIC VARIATION IN HIF SIGNALING UNDERLIES QUANTITATIVE VARIATION IN PHYSIOLOGICAL AND LIFE-HISTORY TRAITS WITHIN LOWLAND BUTTERFLY POPULATIONS

    Evolution

    Volume 67, Issue 4, April 2013, Pages: 1105–1115, James H. Marden, Howard W. Fescemyer, Rudolf J. Schilder, William R. Doerfler, Juan C. Vera and Christopher W. Wheat

    Version of Record online : 11 DEC 2012, DOI: 10.1111/evo.12004

  2. You have free access to this content
    Resistance of glia-like central and peripheral neural stem cells to genetically induced mitochondrial dysfunction—differential effects on neurogenesis

    EMBO reports

    Volume 16, Issue 11, November 2015, Pages: 1511–1519, Blanca Díaz-Castro, Ricardo Pardal, Paula García-Flores, Verónica Sobrino, Rocío Durán, José I Piruat and José López-Barneo

    Version of Record online : 21 SEP 2015, DOI: 10.15252/embr.201540982

  3. Transcription Association of VHL and SDH Mutations Link Hypoxia and Oxidoreductase Signals in Pheochromocytomas

    Annals of the New York Academy of Sciences

    Volume 1073, Issue 1, August 2006, Pages: 208–220, PATRICIA L.M. DAHIA and for the FAMILIAL PHEOCHROMOCYTOMA CONSORTIUM

    Version of Record online : 7 SEP 2006, DOI: 10.1196/annals.1353.023

  4. No difference in phenotype of the main Dutch SDHD founder mutations

    Clinical Endocrinology

    Volume 79, Issue 6, December 2013, Pages: 824–831, L. T. van Hulsteijn, A. C. den Dulk, F. J. Hes, J. P. Bayley, J. C. Jansen and E. P. M. Corssmit

    Version of Record online : 11 MAY 2013, DOI: 10.1111/cen.12223

  5. Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

    Clinical Endocrinology

    Volume 75, Issue 5, November 2011, Pages: 650–655, E. F. Hensen, M. D. Siemers, J. C. Jansen, E. P. M. Corssmit, J. A. Romijn, C. M. J. Tops, A. G. L. van der Mey, P. Devilee, C. J. Cornelisse, J. P. Bayley and A. H. J. T. Vriends

    Version of Record online : 4 OCT 2011, DOI: 10.1111/j.1365-2265.2011.04097.x

  6. Cloning, mapping and association study with carcass traits of the porcine SDHD gene

    Animal Genetics

    Volume 36, Issue 3, June 2005, Pages: 191–195, Z. M. Zhu, J. B. Zhang, K. Li and S. H. Zhao

    Version of Record online : 28 APR 2005, DOI: 10.1111/j.1365-2052.2005.01270.x

  7. Successful daily home hemodialysis patient-care partner dyads: Benefits outweigh burdens

    Hemodialysis International

    Volume 14, Issue 3, July 2010, Pages: 278–288, Meg WISE, Dorian SCHATELL, Kristi KLICKO, Amy BURDAN and Mary SHOWERS

    Version of Record online : 10 MAY 2010, DOI: 10.1111/j.1542-4758.2010.00443.x

  8. Genomic imprinting and environment in hereditary paraganglioma

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 129C, Issue 1, 15 August 2004, Pages: 85–90, Bora E. Baysal

    Version of Record online : 1 JUL 2004, DOI: 10.1002/ajmg.c.30018

  9. Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 255–263, Renee F. Badenhop, Sanjay Cherian, Reginald S.A. Lord, Bora E. Baysal, Peter E.M. Taschner and Peter R. Schofield

    Version of Record online : 27 APR 2001, DOI: 10.1002/gcc.1142

  10. Oxygen Sensing in the Carotid Body

    Annals of the New York Academy of Sciences

    Volume 1177, Issue 1, October 2009, Pages: 119–131, José López-Barneo, Patricia Ortega-Sáenz, Ricardo Pardal, Alberto Pascual, José I. Piruat, Rocío Durán and Raquel Gómez-Díaz

    Version of Record online : 15 OCT 2009, DOI: 10.1111/j.1749-6632.2009.05033.x

  11. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility

    Clinical Endocrinology

    Volume 59, Issue 6, December 2003, Pages: 728–733, Dewi Astuti, Niki Hart-Holden, Farida Latif, Fiona Lalloo, Graeme C. Black, Caron Lim, Anthony Moran, Ashley B. Grossman, Shirley V. Hodgson, Anthony Freemont, Richard Ramsden, Charis Eng, D. Gareth R. Evans and Eamonn R. Maher

    Version of Record online : 20 NOV 2003, DOI: 10.1046/j.1365-2265.2003.01914.x

  12. You have free access to this content
    SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes

    Journal of Internal Medicine

    Volume 266, Issue 1, July 2009, Pages: 19–42, B. Pasini and C. A. Stratakis

    Version of Record online : 7 APR 2009, DOI: 10.1111/j.1365-2796.2009.02111.x

  13. High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands

    Clinical Genetics

    Volume 81, Issue 3, March 2012, Pages: 284–288, EF Hensen, N van Duinen, JC Jansen, EPM Corssmit, CMJ Tops, JA Romijn, AHJT Vriends, AGL van der Mey, CJ Cornelisse, P Devilee and JP Bayley

    Version of Record online : 15 MAR 2011, DOI: 10.1111/j.1399-0004.2011.01653.x

  14. Genetic and clinical characteristics of head and neck paragangliomas in a chinese population

    The Laryngoscope

    Volume 122, Issue 8, August 2012, Pages: 1761–1766, Xiangqian Zheng, Songfeng Wei, Yang Yu, Tingting Xia, Jing Zhao, Songyuan Gao, Yigong Li and Ming Gao

    Version of Record online : 7 MAY 2012, DOI: 10.1002/lary.23360

  15. Pheochromocytoma and functional paraganglioma syndrome: No longer the 10% tumor

    Journal of Surgical Oncology

    Volume 89, Issue 3, 1 March 2005, Pages: 193–201, Elisabeth Edström Elder, Grahame Elder and Catharina Larsson

    Version of Record online : 17 FEB 2005, DOI: 10.1002/jso.20177

  16. Six years' experience with short daily hemodialysis: Do the early improvements persist in the mid and long term?

    Hemodialysis International

    Volume 8, Issue 2, April 2004, Pages: 151–158, Jules Traeger, Roula Galland, Ehsan Delawari, Walid Arkouche and Richard Hadden

    Version of Record online : 22 APR 2004, DOI: 10.1111/j.1492-7535.2004.01089.x

  17. A novel G106D alteration of the SDHD gene in a pedigree with familial paraganglioma

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 22, 15 November 2006, Pages: 2441–2446, Kazumi Ogawa, Kiyoto Shiga, Shigeru Saijo, Takenori Ogawa, Noriko Kimura and Akira Horii

    Version of Record online : 13 OCT 2006, DOI: 10.1002/ajmg.a.31444

  18. Novel SDHD germ-line mutations in pheochromocytoma patients

    European Journal of Clinical Investigation

    Volume 37, Issue 7, July 2007, Pages: 544–551, C. Neumayer, A. Moritz, R. Asari, A. Weinhäusel, T. Hölzenbein, G. Kretschmer, B. Niederle and O. A. Haas

    Version of Record online : 15 JUN 2007, DOI: 10.1111/j.1365-2362.2007.01822.x

  19. New Advances in the Genetics of Pheochromocytoma and Paraganglioma Syndromes

    Annals of the New York Academy of Sciences

    Volume 1073, Issue 1, August 2006, Pages: 112–121, ANNE-PAULE GIMENEZ-ROQUEPLO

    Version of Record online : 7 SEP 2006, DOI: 10.1196/annals.1353.012

  20. Comparative Survival Literature in Intensive Hemodialysis: Limitations and Future Directions

    Seminars in Dialysis

    Volume 24, Issue 6, November/December 2011, Pages: 629–633, Robert P. Pauly, Scott W. Klarenbach and Paul Komenda

    Version of Record online : 8 DEC 2011, DOI: 10.1111/j.1525-139X.2011.01000.x