Search Results - Tobias Carling

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  1. 1
    Thyroid Cancer

    Thyroid Cancer by Tobias Carling, Robert Udelsman

    Published 2013
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  2. 2
    Vitamin D Receptor (VDR) and Parathyroid Hormone Messenger Ribonucleic Acid Levels Correspond to Polymorphic VDR Alleles in Human Parathyroid Tumors<sup>1</sup>

    Vitamin D Receptor (VDR) and Parathyroid Hormone Messenger Ribonucleic Acid Levels Correspond to Polymorphic VDR Alleles in Human Parathyroid Tumors<sup>1</sup> by Tobias Carling, Jonas Rastad, Göran Åkerström, Gunnar Westin

    Published 1998
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  3. 3
    Reduced Parathyroid Vitamin D Receptor Messenger Ribonucleic Acid Levels in Primary and Secondary Hyperparathyroidism*

    Reduced Parathyroid Vitamin D Receptor Messenger Ribonucleic Acid Levels in Primary and Secondary Hyperparathyroidism* by Tobias Carling, Jonas Rastad, Éva Szabó, Gunnar Westin, Göran Åkerström

    Published 2000
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  4. 4
    25-Hydroxyvitamin D<sub>3</sub>-1α-Hydroxylase Expression in Normal and Pathological Parathyroid Glands

    25-Hydroxyvitamin D<sub>3</sub>-1α-Hydroxylase Expression in Normal and Pathological Parathyroid Glands by Ulrika Segersten, Pamela Correa, Martin Hewison, Per Hellman, Henning Dralle, Tobias Carling, Göran Åkerström, Gunnar Westin

    Published 2002
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  5. 5
    The Risk of Second Cancers After Diagnosis of Primary Thyroid Cancer Is Elevated in Thyroid Microcarcinomas

    The Risk of Second Cancers After Diagnosis of Primary Thyroid Cancer Is Elevated in Thyroid Microcarcinomas by Christopher Kim, Xiaofeng Bi, Dongsheng Pan, Yingtai Chen, Tobias Carling, Shuangge Ma, Robert Udelsman, Yawei Zhang

    Published 2012
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  6. 6
    Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing

    Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing by M. Kyle Cromer, Lee F. Starker, Murim Choi, Robert Udelsman, Carol Nelson‐Williams, Richard P. Lifton, Tobias Carling

    Published 2012
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  7. 7
    Tissue Distribution of Human gp330/Megalin, a Putative Ca<sup>2+</sup>-sensing Protein

    Tissue Distribution of Human gp330/Megalin, a Putative Ca<sup>2+</sup>-sensing Protein by Stefan Lundgren, Tobias Carling, Göran Hjälm, Claes Juhlin, Jonas Rastad, Ulla Pihlgren, Lars Rask, Göran Åkerström, Per Hellman

    Published 1997
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  8. 8
    Parathyroid MEN1 Gene Mutations in Relation to Clinical Characteristics of Nonfamilial Primary Hyperparathyroidism1

    Parathyroid MEN1 Gene Mutations in Relation to Clinical Characteristics of Nonfamilial Primary Hyperparathyroidism1 by Tobias Carling, Pamela Correa, Ola Hessman, Jakob Hedberg, Britt Skogseid, Daniel M. Lindberg, Jonas Rastad, Gunnar Westin, Göran Åkerström

    Published 1998
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  9. 9
    Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

    Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism by Lee F. Starker, Tobias Åkerström, William D. Long, Alberto Delgado-Verdugo, Patricia Donovan, Robert Udelsman, Richard P. Lifton, Tobias Carling

    Published 2011
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  10. 10
    The DNA methylome of benign and malignant parathyroid tumors

    The DNA methylome of benign and malignant parathyroid tumors by Lee F. Starker, Jessica Svedlund, Robert Udelsman, Henning Dralle, Göran Åkerström, Gunnar Westin, Richard P. Lifton, Peyman Björklund, Tobias Carling

    Published 2011
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  11. 11
    Familial Hypercalcemia and Hypercalciuria Caused by a Novel Mutation in the Cytoplasmic Tail of the Calcium Receptor*

    Familial Hypercalcemia and Hypercalciuria Caused by a Novel Mutation in the Cytoplasmic Tail of the Calcium Receptor* by Tobias Carling, Éva Szabó, Mei Bai, Peter Ridefelt, Gunnar Westin, Peter Gustavsson, Sunita Trivedi, Per Hellman, Edward M. Brown, Niklas Dahl, Jonas Rastad

    Published 2000
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  12. 12
    The activating TERT promoter mutation C228T is recurrent in subsets of adrenal tumors

    The activating TERT promoter mutation C228T is recurrent in subsets of adrenal tumors by Tiantian Liu, T Brown, C. Christofer Juhlin, Adam Andreasson, Na Wang, Martin Bäckdahl, James M. Healy, Manju L. Prasad, Reju Korah, Tobias Carling, Dawei Xu, Catharina Larsson

    Published 2014
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  13. 13
    BRAFV600E mutation in papillary thyroid microcarcinoma: a genotype–phenotype correlation

    BRAFV600E mutation in papillary thyroid microcarcinoma: a genotype–phenotype correlation by Renu K. Virk, Alison L. Van Dyke, Alexander Finkelstein, Avīnash Prasad, Joanna Gibson, Pei Hui, Constantine G.A. Theoharis, Tobias Carling, Sanziana A. Roman, Julie Ann Sosa, Robert Udelsman, Manju L. Prasad

    Published 2012
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  14. 14
    Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology

    Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology by Norman G. Nicolson, Timothy D. Murtha, Weilai Dong, Johan O. Paulsson, Jungmin Choi, Andrea Barbieri, T Brown, John W. Kunstman, Catharina Larsson, Manju L. Prasad, Reju Korah, Richard P. Lifton, C. Christofer Juhlin, Tobias Carling

    Published 2018
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  15. 15
    Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein–methyltransferase superfamily

    Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein–methyltransferase superfamily by George Steele-Perkins, Wei Fang, Xiao-Hong Yang, Mireille Van Gele, Tobias Carling, Jian Gu, I. Buyse, Jonathon A. Fletcher, Jinsong Liu, Roderick T. Bronson, Robert B. Chadwick, Albert de la Chapelle, Xiao-kun Zhang, Frank Speleman, Shi Huang

    Published 2001
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  16. 16
    Neomorphic effects of recurrent somatic mutations in <i>Yin Yang 1</i> in insulin-producing adenomas

    Neomorphic effects of recurrent somatic mutations in <i>Yin Yang 1</i> in insulin-producing adenomas by M. Kyle Cromer, Murim Choi, Carol Nelson‐Williams, Annabelle L. Fonseca, John W. Kunstman, Reju Korah, John D. Overton, Shrikant Mane, Barton Kenney, Carl D. Malchoff, Peter Stålberg, Göran Åkerström, Gunnar Westin, Per Hellman, Tobias Carling, Peyman Björklund, Richard P. Lifton

    Published 2015
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  17. 17
    Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

    Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing by John W. Kunstman, C. Christofer Juhlin, Gerald Goh, T Brown, Adam Stenman, James M. Healy, Jill C. Rubinstein, Murim Choi, Nimrod Kiss, Carol Nelson‐Williams, Shrikant Mane, David L. Rimm, Manju L. Prasad, Anders Höög, Jan Zedenius, Catharina Larsson, Reju Korah, Richard P. Lifton, Tobias Carling

    Published 2015
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  18. 18
    American Thyroid Association Design and Feasibility of a Prospective Randomized Controlled Trial of Prophylactic Central Lymph Node Dissection for Papillary Thyroid Carcinoma

    American Thyroid Association Design and Feasibility of a Prospective Randomized Controlled Trial of Prophylactic Central Lymph Node Dissection for Papillary Thyroid Carcinoma by Tobias Carling, Sally E. Carty, Maria Ciarleglio, David S. Cooper, Gerard M. Doherty, Lawrence T. Kim, Richard T. Kloos, Ernest L. Mazzaferri, Peter Peduzzi, Sanziana A. Roman, Rebecca S. Sippel, Julie Ann Sosa, Brendan C. Stack, David L. Steward, Ralph P. Tufano, R. Michael Tuttle, for the American Thyroid Robert Udelsman

    Published 2012
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  19. 19
    Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype

    Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype by Ute I. Scholl, James M. Healy, Anne Thiel, Annabelle L. Fonseca, T Brown, John W. Kunstman, Matthew J. Horne, Dimo Dietrich, Jasmin Riemer, S. Kücükköylü, Esther N. Reimer, Anna‐Carinna Reis, Gerald Goh, Glen Kristiansen, Amit Mahajan, Reju Korah, Richard P. Lifton, Manju L. Prasad, Tobias Carling

    Published 2015
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  20. 20
    Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies <i><scp>KMT</scp>2<scp>D</scp></i> as a recurrently mutated gene

    Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies <i><scp>KMT</scp>2<scp>D</scp></i> as a recurrently mutated gene by C. Christofer Juhlin, Adam Stenman, Felix Haglund, Victoria Clark, T Brown, Jacob F. Baranoski, Kaya Bilgüvar, Gerald Goh, Jenny Welander, Fredrika Svahn, Jill C. Rubinstein, Stefano Caramuta, Katsuhito Yasuno, Murat Günel, Martin Bäckdahl, Oliver Gimm, Peter Söderkvist, Manju L. Prasad, Reju Korah, Richard P. Lifton, Tobias Carling

    Published 2015
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