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Simon Pearce

Showing results (31-40 of 43) with videos related to

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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|May 8, 2007
Cytotoxic T-lymphocyte-associated antigen-4 single nucleotide polymorphisms and haplotypes in primary biliary cirrhosisPeter Donaldson, Sivakumar Veeramani, Anna Baragiotta, et al.
Clinical Endocrinology|August 20, 2008
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's diseaseMatthew Roycroft, Marta Fichna, David McDonald, et al.
European Journal of Endocrinology|January 14, 2021
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohortsMarissa Penna-Martinez, Gesine Meyer, Anette Boe Wolff, et al.
BMJ Open|January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trialMichael Cole, Ann Marie Hynes, Denise Howel, et al.
BMC Musculoskeletal Disorders|August 7, 2007
Refining animal models in fracture research: seeking consensus in optimising both animal welfare and scientific validity for appropriate biomedical useJorg A Auer, Allen Goodship, Steven Arnoczky, et al.
The Lancet. Psychiatry|January 5, 2016
Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trialR Hamish McAllister-Williams, Ian M Anderson, Andreas Finkelmeyer, et al.
Plant Physiology|July 17, 2013
Transcriptional dynamics of two seed compartments with opposing roles in Arabidopsis seed germinationBas J W Dekkers, Simon Pearce, R P van Bolderen-Veldkamp, et al.
The Journal of Clinical Endocrinology and Metabolism|June 19, 2008
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrumLindsay W Cole, Yisrael Sidis, ChengKang Zhang, et al.
The Journal of Clinical Investigation|January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismNelly Pitteloud, Richard Quinton, Simon Pearce, et al.
European Journal of Endocrinology|February 27, 2008
Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GOLuigi Bartalena, Lelio Baldeschi, Alison Dickinson, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|May 8, 2007
Cytotoxic T-lymphocyte-associated antigen-4 single nucleotide polymorphisms and haplotypes in primary biliary cirrhosisPeter Donaldson, Sivakumar Veeramani, Anna Baragiotta, et al.
Clinical Endocrinology|August 20, 2008
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's diseaseMatthew Roycroft, Marta Fichna, David McDonald, et al.
European Journal of Endocrinology|January 14, 2021
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohortsMarissa Penna-Martinez, Gesine Meyer, Anette Boe Wolff, et al.
BMJ Open|January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trialMichael Cole, Ann Marie Hynes, Denise Howel, et al.
BMC Musculoskeletal Disorders|August 7, 2007
Refining animal models in fracture research: seeking consensus in optimising both animal welfare and scientific validity for appropriate biomedical useJorg A Auer, Allen Goodship, Steven Arnoczky, et al.
The Lancet. Psychiatry|January 5, 2016
Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trialR Hamish McAllister-Williams, Ian M Anderson, Andreas Finkelmeyer, et al.
Plant Physiology|July 17, 2013
Transcriptional dynamics of two seed compartments with opposing roles in Arabidopsis seed germinationBas J W Dekkers, Simon Pearce, R P van Bolderen-Veldkamp, et al.
The Journal of Clinical Endocrinology and Metabolism|June 19, 2008
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrumLindsay W Cole, Yisrael Sidis, ChengKang Zhang, et al.
The Journal of Clinical Investigation|January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismNelly Pitteloud, Richard Quinton, Simon Pearce, et al.
European Journal of Endocrinology|February 27, 2008
Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GOLuigi Bartalena, Lelio Baldeschi, Alison Dickinson, et al.
Pageof 5