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You searched for subject:(GNAS). Showing records 1 – 16 of 16 total matches.

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1. Hanna, Patrick. GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université Paris-Saclay (ComUE)

GNAS est un locus soumis à empreinte parentale. Ce locus produit différents transcrits et protéines en utilisant des promoteurs distincts. Le transcrit bialléique Gsα, les… (more)

Subjects/Keywords: Gnas; Empreinte parentale; Croissance; MicroRNA; Ippsd; Tipmp; Gnas; Parental imprinting; Growth; MicroRNA; Ippsd; Ipmn

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APA (6th Edition):

Hanna, P. (2018). GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS188

Chicago Manual of Style (16th Edition):

Hanna, Patrick. “GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 13, 2021. http://www.theses.fr/2018SACLS188.

MLA Handbook (7th Edition):

Hanna, Patrick. “GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR.” 2018. Web. 13 Apr 2021.

Vancouver:

Hanna P. GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2018SACLS188.

Council of Science Editors:

Hanna P. GNAS et empreinte parentale : Caractérisation des GNAS-miRNAs et d’une nouvelle DMR : GNAS and Parental Imprinting : Characterization of GNAS-miRNAs and a New DMR. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS188


Universiteit Utrecht

2. Kool, Miriam. Pathogenesis of canine cortisol-secreting adrenocortical tumors.

Degree: 2015, Universiteit Utrecht

 In dogs, hypercortisolism is one of the most frequently observed endocrine disorders, with an estimated incidence of about 1-2 cases per 1000 dogs per year.… (more)

Subjects/Keywords: adrenocortical tumor; hypercortisolism; dog; pathogenesis; Cushing; GNAS; angiogenesis

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APA (6th Edition):

Kool, M. (2015). Pathogenesis of canine cortisol-secreting adrenocortical tumors. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/327013

Chicago Manual of Style (16th Edition):

Kool, Miriam. “Pathogenesis of canine cortisol-secreting adrenocortical tumors.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed April 13, 2021. http://dspace.library.uu.nl:8080/handle/1874/327013.

MLA Handbook (7th Edition):

Kool, Miriam. “Pathogenesis of canine cortisol-secreting adrenocortical tumors.” 2015. Web. 13 Apr 2021.

Vancouver:

Kool M. Pathogenesis of canine cortisol-secreting adrenocortical tumors. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Apr 13]. Available from: http://dspace.library.uu.nl:8080/handle/1874/327013.

Council of Science Editors:

Kool M. Pathogenesis of canine cortisol-secreting adrenocortical tumors. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/327013


University of Toronto

3. Zhang, Lucia. Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model.

Degree: PhD, 2018, University of Toronto

 GαS is a heterotrimeric G protein that transduces signals from cell surface G protein-coupled receptors to stimulate intracellular signaling cascades. Clinically, tight regulation of GαS… (more)

Subjects/Keywords: Biomechanics; Bone; GNAS; G protein; Parathyroid Hormone; Trabecular; 0419

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APA (6th Edition):

Zhang, L. (2018). Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91966

Chicago Manual of Style (16th Edition):

Zhang, Lucia. “Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model.” 2018. Doctoral Dissertation, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/91966.

MLA Handbook (7th Edition):

Zhang, Lucia. “Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model.” 2018. Web. 13 Apr 2021.

Vancouver:

Zhang L. Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/91966.

Council of Science Editors:

Zhang L. Effects of Osteoblast-Specific GαS Overexpression on Skeletal Development and Response to Catabolic and Anabolic Stimuli Using a Transgenic Mouse Model. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91966

4. V. Boldrin. CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES.

Degree: 2017, Università degli Studi di Milano

 Pseudohypoparathyroidism is a term used to identify a heterogeneous group of rare diseases associated with genetic and/or epigenetic defects at the imprinted GNAS locus, that… (more)

Subjects/Keywords: GNAS; mesenchymal stem cells; imprinting; ectopic bone formation; osteoblast; Settore MED/13 - Endocrinologia

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APA (6th Edition):

Boldrin, V. (2017). CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/488739

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Boldrin, V.. “CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES.” 2017. Thesis, Università degli Studi di Milano. Accessed April 13, 2021. http://hdl.handle.net/2434/488739.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Boldrin, V.. “CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES.” 2017. Web. 13 Apr 2021.

Vancouver:

Boldrin V. CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES. [Internet] [Thesis]. Università degli Studi di Milano; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2434/488739.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Boldrin V. CELLULAR DETERMINANTS OF ECTOPIC BONE FORMATION IN ALBRIGHT HEREDITARY OSTEODYSTROPHY, PSEUDOHYPOPARATHYROIDISM AND GNAS-RELATED DISEASES. [Thesis]. Università degli Studi di Milano; 2017. Available from: http://hdl.handle.net/2434/488739

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

5. Motte-Signoret, Emmanuelle. Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene).

Degree: Docteur es, Biologie cellulaire et moléculaire, 2016, Sorbonne Paris Cité

 L’acrodysostose est une chondrodysplasie associant une petite taille et des anomalies des extrémités et de la face. Les mécanismes moléculaires sous-jacents ont récemment été identifiés,… (more)

Subjects/Keywords: Acrodysostose; PDE4D; PRKAR1A; Pseudo-hypoparathyroïdie; GNAS; AMP cyclique; Compartimentalisation cellulaire; Résistance hormonale; Cellular and molecular biology; 576.5

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APA (6th Edition):

Motte-Signoret, E. (2016). Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene). (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB098

Chicago Manual of Style (16th Edition):

Motte-Signoret, Emmanuelle. “Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene).” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed April 13, 2021. http://www.theses.fr/2016USPCB098.

MLA Handbook (7th Edition):

Motte-Signoret, Emmanuelle. “Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene).” 2016. Web. 13 Apr 2021.

Vancouver:

Motte-Signoret E. Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene). [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2016USPCB098.

Council of Science Editors:

Motte-Signoret E. Exploration fonctionnelle in vitro des mécanismes à l'origine de l'acrodysostose sans résistance hormonale par mutation du gène de la PDE4D : comparaison avec l'acrodysostose et résistance plurihormonale (mutations du gène PRKAR1A) et la pseudo-hypoparathyroïdie 1a (mutations du gène GNAS) : In vitro functional exploration of mechanisms causing acrodysostosis without hormonal resistance by mutation of the PDE4D gene : comparison with acrodysostosis and multi-hormonal resistance (mutations of the PRKAR1A gene) and pseudo-hypoparathyroidism 1a (mutations in the GNAS gene). [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB098


Freie Universität Berlin

6. Akdeniz, Sinan. Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie.

Degree: 2015, Freie Universität Berlin

 Unsere Untersuchung von ADSCs und ihrer genotyp-spezifischen Fähigkeit zur adipogenetischen Differenzierung hat auf ein gesteigertes adipogenetisches Potential für aus paternalen E2KO-Mäusen stammende ADSCs und ein… (more)

Subjects/Keywords: progressive osseous heteroplasia; adipose-derived stromal cells; Gnas; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Akdeniz, S. (2015). Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-4852

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Akdeniz, Sinan. “Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie.” 2015. Thesis, Freie Universität Berlin. Accessed April 13, 2021. http://dx.doi.org/10.17169/refubium-4852.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Akdeniz, Sinan. “Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie.” 2015. Web. 13 Apr 2021.

Vancouver:

Akdeniz S. Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 13]. Available from: http://dx.doi.org/10.17169/refubium-4852.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Akdeniz S. Implikationen für die Pathogenese der progressiven knöchernen Heteroplasie. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-4852

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

7. Kool, Miriam. Pathogenesis of canine cortisol-secreting adrenocortical tumors.

Degree: 2015, University Utrecht

 In dogs, hypercortisolism is one of the most frequently observed endocrine disorders, with an estimated incidence of about 1-2 cases per 1000 dogs per year.… (more)

Subjects/Keywords: adrenocortical tumor; hypercortisolism; dog; pathogenesis; Cushing; GNAS; angiogenesis

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APA (6th Edition):

Kool, M. (2015). Pathogenesis of canine cortisol-secreting adrenocortical tumors. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/327013 ; URN:NBN:NL:UI:10-1874-327013 ; 1874/327013 ; urn:isbn:9789462595347 ; URN:NBN:NL:UI:10-1874-327013 ; https://dspace.library.uu.nl/handle/1874/327013

Chicago Manual of Style (16th Edition):

Kool, Miriam. “Pathogenesis of canine cortisol-secreting adrenocortical tumors.” 2015. Doctoral Dissertation, University Utrecht. Accessed April 13, 2021. https://dspace.library.uu.nl/handle/1874/327013 ; URN:NBN:NL:UI:10-1874-327013 ; 1874/327013 ; urn:isbn:9789462595347 ; URN:NBN:NL:UI:10-1874-327013 ; https://dspace.library.uu.nl/handle/1874/327013.

MLA Handbook (7th Edition):

Kool, Miriam. “Pathogenesis of canine cortisol-secreting adrenocortical tumors.” 2015. Web. 13 Apr 2021.

Vancouver:

Kool M. Pathogenesis of canine cortisol-secreting adrenocortical tumors. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Apr 13]. Available from: https://dspace.library.uu.nl/handle/1874/327013 ; URN:NBN:NL:UI:10-1874-327013 ; 1874/327013 ; urn:isbn:9789462595347 ; URN:NBN:NL:UI:10-1874-327013 ; https://dspace.library.uu.nl/handle/1874/327013.

Council of Science Editors:

Kool M. Pathogenesis of canine cortisol-secreting adrenocortical tumors. [Doctoral Dissertation]. University Utrecht; 2015. Available from: https://dspace.library.uu.nl/handle/1874/327013 ; URN:NBN:NL:UI:10-1874-327013 ; 1874/327013 ; urn:isbn:9789462595347 ; URN:NBN:NL:UI:10-1874-327013 ; https://dspace.library.uu.nl/handle/1874/327013

8. Nault, Jean-Charles. Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors.

Degree: Docteur es, Hématologie et oncologie, 2015, Sorbonne Paris Cité

Les adénomes hépatocellulaires (AHC) sont des tumeurs hépatiques bénignes rares se développant chez la femme jeune suite à la prise de contraceptifs oraux et pouvant… (more)

Subjects/Keywords: Adénome hépatocellulaire; JAK/STAT; GNAS; TERT; Transformation maligne; Carcinome hépatocellulaire; Score 5-gène; Pronostic moléculaire; AAV2; Mutagénèse insertionnelle; Hepatocellular adenoma; JAK/STAT; GNAS; TERT; Malignant transformation; Hepatocellular carcinoma; 5-gene score; Molecular signature; AAV2; Insertional mutagenesis; 616.994

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APA (6th Edition):

Nault, J. (2015). Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2015USPCB122

Chicago Manual of Style (16th Edition):

Nault, Jean-Charles. “Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors.” 2015. Doctoral Dissertation, Sorbonne Paris Cité. Accessed April 13, 2021. http://www.theses.fr/2015USPCB122.

MLA Handbook (7th Edition):

Nault, Jean-Charles. “Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors.” 2015. Web. 13 Apr 2021.

Vancouver:

Nault J. Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2015. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2015USPCB122.

Council of Science Editors:

Nault J. Identification de nouveaux mécanismes de carcinogénèse et facteurs pronostiques des tumeurs hépatocellulaires : Identification of new mechanisms of carcinogenesis and new prognostic biomarkers in hepatocellular tumors. [Doctoral Dissertation]. Sorbonne Paris Cité; 2015. Available from: http://www.theses.fr/2015USPCB122

9. Pilati, Camilla. Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas.

Degree: Docteur es, Hématologie et oncologie, 2013, Université Paris Descartes – Paris V

 Les adénomes hépatocellulaires (AHC) sont des tumeurs bénignes rares qui se développent le plus souvent chez la femme jeune suite à la prise de contraceptifs… (more)

Subjects/Keywords: Adénome hépatocellulaire; JAK/STAT; Gp130; STAT3; GNAS; FRK; JAK1; CTNNB1; TERT; Transformation maligne; Carcinome hépatocellulaire; Hepatocellular adenoma; JAK/STAT; Gp130; STAT3; GNAS; FRK; JAK1; CTNNB1; TERT; Malignant transformation; Hepatocellular carcinoma; 616.993

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APA (6th Edition):

Pilati, C. (2013). Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05S011

Chicago Manual of Style (16th Edition):

Pilati, Camilla. “Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed April 13, 2021. http://www.theses.fr/2013PA05S011.

MLA Handbook (7th Edition):

Pilati, Camilla. “Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas.” 2013. Web. 13 Apr 2021.

Vancouver:

Pilati C. Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2013PA05S011.

Council of Science Editors:

Pilati C. Caractérisation moléculaire des adénomes hépatocellulaires : Molecular characterization of hepatocellular adenomas. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05S011

10. Romanet, Pauline. Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus.

Degree: Docteur es, Neurosciences, 2018, Aix Marseille Université

La Néoplasie Endocrinienne Multiple de type 1 (NEM1) est une maladie génétique qui associe hyperparathyroïdie primaire, tumeurs neuroendocrines digestives et adénomes hypophysaires. Elle est due… (more)

Subjects/Keywords: Men1; Gnas; Syndrome de McCune-Albright; Génétique; Database; ADN circulant; Adénome hypophysaire; Nem1; Néoplasme Endocrinienne Multiple de type 1; Empreinte; Gnas; Men1; McCune-Albright; Genetics; Database; Cell-Free circulating DNA; Pituitary adenomas; Imprinting locus

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APA (6th Edition):

Romanet, P. (2018). Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2018AIXM0278

Chicago Manual of Style (16th Edition):

Romanet, Pauline. “Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus.” 2018. Doctoral Dissertation, Aix Marseille Université. Accessed April 13, 2021. http://www.theses.fr/2018AIXM0278.

MLA Handbook (7th Edition):

Romanet, Pauline. “Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus.” 2018. Web. 13 Apr 2021.

Vancouver:

Romanet P. Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus. [Internet] [Doctoral dissertation]. Aix Marseille Université 2018. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2018AIXM0278.

Council of Science Editors:

Romanet P. Etiologies héréditaires et somatiques des adénomes hypophysaires : étude du gène Men1 et du locus Gnas : Hereditary and somatic etiologies of pituitary adenomas : study of the Men1 gene and the Gnas locus. [Doctoral Dissertation]. Aix Marseille Université 2018. Available from: http://www.theses.fr/2018AIXM0278


Université Paris-Sud – Paris XI

11. Grybek, Virginie. Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance.

Degree: Docteur es, Sciences de la vie et de la santé, 2015, Université Paris-Sud – Paris XI

GNAS est un locus complexe soumis à l'empreinte parentale. Il code pour cinq transcrits alternatifs dont l’expression est régulée de manière parentale, tissulaire et développementale… (more)

Subjects/Keywords: GNAS; Empreinte parentale; Pseudohypoparathyroïdie; Croissance fœtale; Croissance post-natale; Cellules souches embryonnaires; Cellules souches pluripotentes induites; GNAS; Parental imprinting; Pseudohypoparathyroidism; Fetal growth; Postnatal growth; Embryonic stem cells; Pluripotent induced stem cells

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Grybek, V. (2015). Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA11T002

Chicago Manual of Style (16th Edition):

Grybek, Virginie. “Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 13, 2021. http://www.theses.fr/2015PA11T002.

MLA Handbook (7th Edition):

Grybek, Virginie. “Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance.” 2015. Web. 13 Apr 2021.

Vancouver:

Grybek V. Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2015PA11T002.

Council of Science Editors:

Grybek V. Etude d’un locus soumis à empreinte parentale : le locus GNAS. Rôle des transcrits et maintien de l’empreinte : Study of a Human Imprinted Locus : the GNAS Locus. Role of the GNAS Transcripts and Imprinting Maintenance. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA11T002

12. Mariana Tenorio Antunes Reis. Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP).

Degree: 2014, University of São Paulo

 INTRODUÇÃO: A primeira doença humana atribuída à resistência hormonal foi o pseudo-hipoparatireoidismo (PHP), uma doença rara caracterizada por hipocalcemia, hiperfosfatemia e níveis elevados de hormônio… (more)

Subjects/Keywords: Hiperfosfatemia; Hipocalcemia; Hormônio paratireóideo; Osteodistrofia hereditária de Albright; Proteína GNAS humana; Proteína-G estimuladora Gs; Pseudo-hipoparatireoidismo; Pseudopseudo-hipoparatireoidismo; Albright hereditary osteodystrophy; G-Protein/stimulatory Gs; GNAS protein/human; Hyperphosphatemia; Hypocalcemia; Parathyroid hormone; Pseudohypoparathyroidism; Pseudopseudohypoparathyroidism

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Reis, M. T. A. (2014). Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP). (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-26022015-153923/

Chicago Manual of Style (16th Edition):

Reis, Mariana Tenorio Antunes. “Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP).” 2014. Doctoral Dissertation, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-26022015-153923/.

MLA Handbook (7th Edition):

Reis, Mariana Tenorio Antunes. “Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP).” 2014. Web. 13 Apr 2021.

Vancouver:

Reis MTA. Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP). [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-26022015-153923/.

Council of Science Editors:

Reis MTA. Avaliação fenotípica e de defeitos moleculares no GNAS em pacientes com pseudo-hipoparatireoidismo (PHP) e pseudopseudo-hipoparatireoidismo (PPHP). [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-26022015-153923/


Freie Universität Berlin

13. Thormeyer, Vera. Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose.

Degree: 2019, Freie Universität Berlin

 The congenital hypothyroidism is the most common neonatal endocrine disorder with an incidence of 1:4000 – 1:3000 worldwide. The disease is primarly caused by a… (more)

Subjects/Keywords: congenital hypothyroidism; DNA methylation; pyrosequencing; GNAS; monozygotic twins; hypothyroidism; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Thormeyer, V. (2019). Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-1870

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Thormeyer, Vera. “Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose.” 2019. Thesis, Freie Universität Berlin. Accessed April 13, 2021. http://dx.doi.org/10.17169/refubium-1870.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Thormeyer, Vera. “Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose.” 2019. Web. 13 Apr 2021.

Vancouver:

Thormeyer V. Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose. [Internet] [Thesis]. Freie Universität Berlin; 2019. [cited 2021 Apr 13]. Available from: http://dx.doi.org/10.17169/refubium-1870.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Thormeyer V. Analyse der DNA-Methylierung des GNAS-Gens bei diskordanten, monozygoten Zwillingen mit kongenitaler Hypothyreose. [Thesis]. Freie Universität Berlin; 2019. Available from: http://dx.doi.org/10.17169/refubium-1870

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Leiden University

14. Majoor, B.C.J. Fibrous dysplasia.

Degree: 2018, Leiden University

  <table width="100%"> <tbody><tr> <td> Fibrous dysplasia is a heterogeneous rare bone disorder that is caused by the mosaic distribution of a postzygotic mutation of… (more)

Subjects/Keywords: Fibrous Dysplasia; McCune-Albright syndrome; Mazabraud's syndrome; GNAS-gene; Rare bone disease

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Majoor, B. C. J. (2018). Fibrous dysplasia. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/62059

Chicago Manual of Style (16th Edition):

Majoor, B C J. “Fibrous dysplasia.” 2018. Doctoral Dissertation, Leiden University. Accessed April 13, 2021. http://hdl.handle.net/1887/62059.

MLA Handbook (7th Edition):

Majoor, B C J. “Fibrous dysplasia.” 2018. Web. 13 Apr 2021.

Vancouver:

Majoor BCJ. Fibrous dysplasia. [Internet] [Doctoral dissertation]. Leiden University; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1887/62059.

Council of Science Editors:

Majoor BCJ. Fibrous dysplasia. [Doctoral Dissertation]. Leiden University; 2018. Available from: http://hdl.handle.net/1887/62059


University of Queensland

15. Liu, Cheng. Molecular characterisation of serrated precursors in colorectal carcinoma.

Degree: Faculty of Medicine, 2020, University of Queensland

Subjects/Keywords: SSA; SSAD; TSA; Colorectal carcinoma; BRAF; KRAS; GNAS; MLH1; Methylation; Array; 1112 Oncology and Carcinogenesis

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APA (6th Edition):

Liu, C. (2020). Molecular characterisation of serrated precursors in colorectal carcinoma. (Thesis). University of Queensland. Retrieved from https://espace.library.uq.edu.au/view/UQ:aa23173/thumbnail_s44214735_final_thesis_t.jpg ; https://espace.library.uq.edu.au/view/UQ:aa23173/s44214735_final_thesis.pdf ; https://espace.library.uq.edu.au/view/UQ:aa23173

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Liu, Cheng. “Molecular characterisation of serrated precursors in colorectal carcinoma.” 2020. Thesis, University of Queensland. Accessed April 13, 2021. https://espace.library.uq.edu.au/view/UQ:aa23173/thumbnail_s44214735_final_thesis_t.jpg ; https://espace.library.uq.edu.au/view/UQ:aa23173/s44214735_final_thesis.pdf ; https://espace.library.uq.edu.au/view/UQ:aa23173.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Liu, Cheng. “Molecular characterisation of serrated precursors in colorectal carcinoma.” 2020. Web. 13 Apr 2021.

Vancouver:

Liu C. Molecular characterisation of serrated precursors in colorectal carcinoma. [Internet] [Thesis]. University of Queensland; 2020. [cited 2021 Apr 13]. Available from: https://espace.library.uq.edu.au/view/UQ:aa23173/thumbnail_s44214735_final_thesis_t.jpg ; https://espace.library.uq.edu.au/view/UQ:aa23173/s44214735_final_thesis.pdf ; https://espace.library.uq.edu.au/view/UQ:aa23173.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Liu C. Molecular characterisation of serrated precursors in colorectal carcinoma. [Thesis]. University of Queensland; 2020. Available from: https://espace.library.uq.edu.au/view/UQ:aa23173/thumbnail_s44214735_final_thesis_t.jpg ; https://espace.library.uq.edu.au/view/UQ:aa23173/s44214735_final_thesis.pdf ; https://espace.library.uq.edu.au/view/UQ:aa23173

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University

16. Isobe, Yuu. Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia .

Degree: 2019, Kyoto University

Subjects/Keywords: Fibrous dysplasia; GNAS (guanine nucleotide-binding protein; alpha; stimulating activity polypeptide 1); MFD (monostotic fibrous dysplasia); Arg201 (arginine 201)

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Isobe, Y. (2019). Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Isobe, Yuu. “Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia .” 2019. Thesis, Kyoto University. Accessed April 13, 2021. http://hdl.handle.net/2433/242351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Isobe, Yuu. “Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia .” 2019. Web. 13 Apr 2021.

Vancouver:

Isobe Y. Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia . [Internet] [Thesis]. Kyoto University; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/242351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Isobe Y. Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.