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You searched for subject:(Matriptase). Showing records 1 – 17 of 17 total matches.

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Université de Sherbrooke

1. Beaulieu, Alexandre. Étude du clivage de l'hémagglutinine de l'influenza par la matriptase .

Degree: 2013, Université de Sherbrooke

 Le virus de l’influenza infecte chaque année des millions d'humains ce qui a des impacts pour l’économie et entraîne le décès de nombreux individus. Le… (more)

Subjects/Keywords: TTSP; Hémagglutinine; Matriptase; Influenza

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APA (6th Edition):

Beaulieu, A. (2013). Étude du clivage de l'hémagglutinine de l'influenza par la matriptase . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/6666

Chicago Manual of Style (16th Edition):

Beaulieu, Alexandre. “Étude du clivage de l'hémagglutinine de l'influenza par la matriptase .” 2013. Masters Thesis, Université de Sherbrooke. Accessed October 18, 2019. http://hdl.handle.net/11143/6666.

MLA Handbook (7th Edition):

Beaulieu, Alexandre. “Étude du clivage de l'hémagglutinine de l'influenza par la matriptase .” 2013. Web. 18 Oct 2019.

Vancouver:

Beaulieu A. Étude du clivage de l'hémagglutinine de l'influenza par la matriptase . [Internet] [Masters thesis]. Université de Sherbrooke; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11143/6666.

Council of Science Editors:

Beaulieu A. Étude du clivage de l'hémagglutinine de l'influenza par la matriptase . [Masters Thesis]. Université de Sherbrooke; 2013. Available from: http://hdl.handle.net/11143/6666

2. 松下, 巧. Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現.

Degree: 博士(歯学), 2017, Osaka Dental University / 大阪歯科大学

Development of the salivary gland is characterized by extensive branching morphogenesis and lumen formation as well as differentiation into acinar and ductal cells. Although various… (more)

Subjects/Keywords: Grhl2; SPINT1; Matriptase; Salivary gland; Development

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APA (6th Edition):

松下, . (2017). Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現. (Thesis). Osaka Dental University / 大阪歯科大学. Retrieved from http://id.nii.ac.jp/1392/00000147/

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):

松下, 巧. “Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現.” 2017. Thesis, Osaka Dental University / 大阪歯科大学. Accessed October 18, 2019. http://id.nii.ac.jp/1392/00000147/.

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

MLA Handbook (7th Edition):

松下, 巧. “Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現.” 2017. Web. 18 Oct 2019.

Vancouver:

松下 . Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現. [Internet] [Thesis]. Osaka Dental University / 大阪歯科大学; 2017. [cited 2019 Oct 18]. Available from: http://id.nii.ac.jp/1392/00000147/.

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

Council of Science Editors:

松下 . Expression of Grhl2 and Its Target Gene Products in Developing Mouse Submandibular Gland : マウス顎下腺発生過程における転写因子 Grhl2 とその標的遺伝子の発現. [Thesis]. Osaka Dental University / 大阪歯科大学; 2017. Available from: http://id.nii.ac.jp/1392/00000147/

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

3. Lenoir, Anne. Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism.

Degree: Docteur es, Physiologie, 2013, Université Paris Descartes – Paris V

Dans l’organisme, le fer assure le transport d’oxygène jusqu’à tous les organes, via l’hémoglobine des globules rouges. L’hepcidine, une hormone hépatique hyposidérémiante, contrôle le taux… (more)

Subjects/Keywords: TMPRSS6; Matriptase-2; Anémie; IRIDA; Hepcidine; Fer; TMPRSS6; Matriptase-2; Anemia; IRIDA; Hepcidin; Iron; 611.018 1

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APA (6th Edition):

Lenoir, A. (2013). Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T066

Chicago Manual of Style (16th Edition):

Lenoir, Anne. “Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 18, 2019. http://www.theses.fr/2013PA05T066.

MLA Handbook (7th Edition):

Lenoir, Anne. “Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism.” 2013. Web. 18 Oct 2019.

Vancouver:

Lenoir A. Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2013PA05T066.

Council of Science Editors:

Lenoir A. Etude des mécanismes régulateurs de l’activité de la Matriptase-2 : recherche de ses partenaires impliqués dans le métabolisme du fer : Study of regulatory mechanisms of Matriptase-2 activity : search of its partners implied in iron metabolism. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T066


Université de Sherbrooke

4. Béliveau, François. Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer .

Degree: 2012, Université de Sherbrooke

 Les protéases à sérine transmembranaires de type II (TTSP) forment une famille d'enzymes protéolytiques nouvellement identifiée dont les rôles physiologiques restent encore peu connus. Ces… (more)

Subjects/Keywords: Internalisation; Spécificité enzymatique; TMPRSS6; Matriptase-2; Protéase; TTSP

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APA (6th Edition):

Béliveau, F. (2012). Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer . (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/6224

Chicago Manual of Style (16th Edition):

Béliveau, François. “Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer .” 2012. Doctoral Dissertation, Université de Sherbrooke. Accessed October 18, 2019. http://hdl.handle.net/11143/6224.

MLA Handbook (7th Edition):

Béliveau, François. “Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer .” 2012. Web. 18 Oct 2019.

Vancouver:

Béliveau F. Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer . [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11143/6224.

Council of Science Editors:

Béliveau F. Spécificité enzymatique et régulation fonctionnelle de la matriptase-2, une protéase à sérine transmembranaire de type II essentielle à l'homéostasie du fer . [Doctoral Dissertation]. Université de Sherbrooke; 2012. Available from: http://hdl.handle.net/11143/6224


Université de Sherbrooke

5. Colombo, Éloïc. Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase .

Degree: 2019, Université de Sherbrooke

 La matriptase est une enzyme appartenant à la famille des protéases à sérine transmembranaires de type II (TTSPs) et joue un rôle physiologique important dans… (more)

Subjects/Keywords: TTSPs; Matriptase; Inhibiteur peptidomimétique à liaison forte; Sélectivité; Anti-influenza

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APA (6th Edition):

Colombo, . (2019). Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase . (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/14514

Chicago Manual of Style (16th Edition):

Colombo, Éloïc. “Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase .” 2019. Doctoral Dissertation, Université de Sherbrooke. Accessed October 18, 2019. http://hdl.handle.net/11143/14514.

MLA Handbook (7th Edition):

Colombo, Éloïc. “Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase .” 2019. Web. 18 Oct 2019.

Vancouver:

Colombo . Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase . [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11143/14514.

Council of Science Editors:

Colombo . Conception, synthèse et caractérisation biologique d'inhibiteurs peptidomimétiques de la matriptase . [Doctoral Dissertation]. Université de Sherbrooke; 2019. Available from: http://hdl.handle.net/11143/14514


Wayne State University

6. Conley-Lacomb, M. Katie. Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression.

Degree: PhD, Cancer Biology, 2010, Wayne State University

  Platelet Derived Growth Factor (PDGF) is a family of mesenchymal growth factors that regulate cell proliferation, migration, and differentiation. Unlike the classic PDGF ligands… (more)

Subjects/Keywords: Growth Factors; Matriptase; PDGF D; Protease; PTEN; Cell Biology

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APA (6th Edition):

Conley-Lacomb, M. K. (2010). Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/58

Chicago Manual of Style (16th Edition):

Conley-Lacomb, M Katie. “Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression.” 2010. Doctoral Dissertation, Wayne State University. Accessed October 18, 2019. https://digitalcommons.wayne.edu/oa_dissertations/58.

MLA Handbook (7th Edition):

Conley-Lacomb, M Katie. “Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression.” 2010. Web. 18 Oct 2019.

Vancouver:

Conley-Lacomb MK. Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression. [Internet] [Doctoral dissertation]. Wayne State University; 2010. [cited 2019 Oct 18]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/58.

Council of Science Editors:

Conley-Lacomb MK. Matriptase/pdgf D/beta-Pdgfr Signaling Axis In Human Prostate Cancer: The Role Of Pten In The Regulation Of Pdgf D Expression. [Doctoral Dissertation]. Wayne State University; 2010. Available from: https://digitalcommons.wayne.edu/oa_dissertations/58


University of California – San Francisco

7. Darragh, Molly Rose. Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>.

Degree: Biophysics, 2010, University of California – San Francisco

 Cancer is a disease which develops as the result of many negative changes in the biology of otherwise healthy tissue. Non-invasive imaging of aberrant, tumor-associated… (more)

Subjects/Keywords: Biology, Molecular; Cancer; Matriptase; Molecular Imaging; Protease; Protease Activity

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APA (6th Edition):

Darragh, M. R. (2010). Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/69q0228b

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):

Darragh, Molly Rose. “Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>.” 2010. Thesis, University of California – San Francisco. Accessed October 18, 2019. http://www.escholarship.org/uc/item/69q0228b.

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

MLA Handbook (7th Edition):

Darragh, Molly Rose. “Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>.” 2010. Web. 18 Oct 2019.

Vancouver:

Darragh MR. Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/69q0228b.

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

Council of Science Editors:

Darragh MR. Targeting the Active Serine Protease MT-SP1 for Tumor Detection <italics>in vivo</italics>. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/69q0228b

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

8. Menou, Awen. Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie. Biomolécules et thérapeutiques, 2017, Sorbonne Paris Cité

La Fibrose Pulmonaire Idiopathique (FPI) est une pathologie pulmonaire chronique, progressive, irréversible et mortelle, dont les thérapeutiques sont insuffisantes à ce jour. L'activation de la… (more)

Subjects/Keywords: TTSPs; Matriptase; Human Airway Trypsin-like protease; HAT; Récepteur 2 activé par des protéases; PAR-2; TTSPs; Matriptase; Human Airway Trypsin-like protease; HAT; Protease-Activated Receptor-2; PAR-2

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APA (6th Edition):

Menou, A. (2017). Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC020

Chicago Manual of Style (16th Edition):

Menou, Awen. “Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 18, 2019. http://www.theses.fr/2017USPCC020.

MLA Handbook (7th Edition):

Menou, Awen. “Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis.” 2017. Web. 18 Oct 2019.

Vancouver:

Menou A. Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2017USPCC020.

Council of Science Editors:

Menou A. Implication des protéases à sérine de la famille des Type II Transmembrane Serine Proteases dans la Fibrose Pulmonaire Idiopathique : Serine proteases of the Type II Transmembrane Serine Proteases family involvement in Idiopathic Pulmonary Fibrosis. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC020

9. Cheung, Ka-chun. Role of matriptase (ST14) in chronic myeloid leukaemia.

Degree: 2014, University of Adelaide

 Chronic myeloid leukaemia (CML) is characterised by a reciprocal chromosomal translocation that gives rise to a 22q-, or Philadelphia (Ph) chromosome and a derivative 9+.… (more)

Subjects/Keywords: matriptase; ST14; chronic myeloid leukaemia

matriptase, acts as a tumour suppressor gene in solid tumours, but has also been linked to… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

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APA (6th Edition):

Cheung, K. (2014). Role of matriptase (ST14) in chronic myeloid leukaemia. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/85926

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):

Cheung, Ka-chun. “Role of matriptase (ST14) in chronic myeloid leukaemia.” 2014. Thesis, University of Adelaide. Accessed October 18, 2019. http://hdl.handle.net/2440/85926.

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

MLA Handbook (7th Edition):

Cheung, Ka-chun. “Role of matriptase (ST14) in chronic myeloid leukaemia.” 2014. Web. 18 Oct 2019.

Vancouver:

Cheung K. Role of matriptase (ST14) in chronic myeloid leukaemia. [Internet] [Thesis]. University of Adelaide; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2440/85926.

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

Council of Science Editors:

Cheung K. Role of matriptase (ST14) in chronic myeloid leukaemia. [Thesis]. University of Adelaide; 2014. Available from: http://hdl.handle.net/2440/85926

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


University of California – San Francisco

10. Barker, Adrian. Protease-activated receptor-2 (PAR2) in epithelial biology.

Degree: Biomedical Sciences, 2013, University of California – San Francisco

 Protease-activated receptor-2 is a G-protein-coupled receptor involved in inflammatory and pain responses, as well as pathogenesis in the gastrointestinal and cardiovascular systems, among others. Efforts… (more)

Subjects/Keywords: Developmental biology; Cellular biology; epithelial cell extrusion; epithelium; HAI1; matriptase; PAR2; zebrafish

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APA (6th Edition):

Barker, A. (2013). Protease-activated receptor-2 (PAR2) in epithelial biology. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2b49z9sm

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):

Barker, Adrian. “Protease-activated receptor-2 (PAR2) in epithelial biology.” 2013. Thesis, University of California – San Francisco. Accessed October 18, 2019. http://www.escholarship.org/uc/item/2b49z9sm.

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

MLA Handbook (7th Edition):

Barker, Adrian. “Protease-activated receptor-2 (PAR2) in epithelial biology.” 2013. Web. 18 Oct 2019.

Vancouver:

Barker A. Protease-activated receptor-2 (PAR2) in epithelial biology. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/2b49z9sm.

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

Council of Science Editors:

Barker A. Protease-activated receptor-2 (PAR2) in epithelial biology. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/2b49z9sm

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

11. St-Georges, Catherine. Optimisation d'inhibiteurs de la matriptase-2 .

Degree: 2017, Université de Sherbrooke

 L’hémochromatose est une maladie héréditaire caractérisée par une surcharge de fer dans l’organisme. Chez une personne saine, l’excès de fer est excrété au niveau des… (more)

Subjects/Keywords: Matriptase-2; Matriptase; Hepsine; Inhibiteurs; Sélectivité; Peptidomimétiques; Piège à sérine; Cétobenzothiazole

…11 I.3 La matriptase-2… …15 I.3.1.3. La régulation du fer par la matriptase-2… …20 I.4 La matriptase et l’hepsine… …21 I.5 Les inhibiteurs naturels de la matriptase-2… …23 I.6 Les inhibiteurs synthétiques de la matriptase-2… 

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APA (6th Edition):

St-Georges, C. (2017). Optimisation d'inhibiteurs de la matriptase-2 . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/10504

Chicago Manual of Style (16th Edition):

St-Georges, Catherine. “Optimisation d'inhibiteurs de la matriptase-2 .” 2017. Masters Thesis, Université de Sherbrooke. Accessed October 18, 2019. http://hdl.handle.net/11143/10504.

MLA Handbook (7th Edition):

St-Georges, Catherine. “Optimisation d'inhibiteurs de la matriptase-2 .” 2017. Web. 18 Oct 2019.

Vancouver:

St-Georges C. Optimisation d'inhibiteurs de la matriptase-2 . [Internet] [Masters thesis]. Université de Sherbrooke; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11143/10504.

Council of Science Editors:

St-Georges C. Optimisation d'inhibiteurs de la matriptase-2 . [Masters Thesis]. Université de Sherbrooke; 2017. Available from: http://hdl.handle.net/11143/10504


Kyoto University / 京都大学

12. Kojima, Kenji. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究.

Degree: 博士(農学), 2014, Kyoto University / 京都大学

新制・論文博士

乙第12878号

論農博第2805号

Subjects/Keywords: protein engineering; matriptase; hepatocyte growth factor activator inhibitor type 1; thermolysin; mutant

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APA (6th Edition):

Kojima, K. (2014). Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/193550 ; http://dx.doi.org/10.14989/doctor.r12878

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):

Kojima, Kenji. “Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究.” 2014. Thesis, Kyoto University / 京都大学. Accessed October 18, 2019. http://hdl.handle.net/2433/193550 ; http://dx.doi.org/10.14989/doctor.r12878.

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

MLA Handbook (7th Edition):

Kojima, Kenji. “Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究.” 2014. Web. 18 Oct 2019.

Vancouver:

Kojima K. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2433/193550 ; http://dx.doi.org/10.14989/doctor.r12878.

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

Council of Science Editors:

Kojima K. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 : サーモライシン、マトリプターゼおよび肝細胞増殖因子活性化因子阻害物質タイプ1の構造と機能に関するタンパク質工学的研究. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/193550 ; http://dx.doi.org/10.14989/doctor.r12878

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

13. Maxson, Julia Elizabeth. Processing and trafficking of the iron regulatory protein, hemojuvelin.

Degree: PhD, 2011, Oregon Health Sciences University

Subjects/Keywords: Membrane proteins; Hemojuvelin; Furin; Matriptase-2; Membrane Proteins; Protein Transport; Iron-Regulatory Proteins

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APA (6th Edition):

Maxson, J. E. (2011). Processing and trafficking of the iron regulatory protein, hemojuvelin. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667

Chicago Manual of Style (16th Edition):

Maxson, Julia Elizabeth. “Processing and trafficking of the iron regulatory protein, hemojuvelin.” 2011. Doctoral Dissertation, Oregon Health Sciences University. Accessed October 18, 2019. doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667.

MLA Handbook (7th Edition):

Maxson, Julia Elizabeth. “Processing and trafficking of the iron regulatory protein, hemojuvelin.” 2011. Web. 18 Oct 2019.

Vancouver:

Maxson JE. Processing and trafficking of the iron regulatory protein, hemojuvelin. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2011. [cited 2019 Oct 18]. Available from: doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667.

Council of Science Editors:

Maxson JE. Processing and trafficking of the iron regulatory protein, hemojuvelin. [Doctoral Dissertation]. Oregon Health Sciences University; 2011. Available from: doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667


Kyoto University

14. Kojima, Kenji. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 .

Degree: 2014, Kyoto University

Subjects/Keywords: protein engineering; matriptase; hepatocyte growth factor activator inhibitor type 1; thermolysin; mutant

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

APA (6th Edition):

Kojima, K. (2014). Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/193550

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):

Kojima, Kenji. “Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 .” 2014. Thesis, Kyoto University. Accessed October 18, 2019. http://hdl.handle.net/2433/193550.

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

MLA Handbook (7th Edition):

Kojima, Kenji. “Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 .” 2014. Web. 18 Oct 2019.

Vancouver:

Kojima K. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 . [Internet] [Thesis]. Kyoto University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2433/193550.

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

Council of Science Editors:

Kojima K. Protein Engineering Studies on Structure and Function of Thermolysin, Matriptase, and Hepatocyte Growth Factor Activator Inhibitor Type 1 . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/193550

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


Université de Sherbrooke

15. Gravel, Emilie. Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance .

Degree: 2016, Université de Sherbrooke

 Résumé: Chaque année, les épidémies saisonnières d’influenza causent de 3 à 5 millions de cas sévères de maladie, entraînant entre 250 000 et 500 000… (more)

Subjects/Keywords: Influenza; Hémagglutinine; Protéases à sérine transmembranaires de type II (TTSP); Matriptase; Hepsine; Clivage protéolytique; Inhibiteur; Résistance; Hemagglutinin; Type II transmembrane serine proteases (TTSP); Hepsin; Proteolytic cleavage; Inhibitor; Resistance

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APA (6th Edition):

Gravel, E. (2016). Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/9464

Chicago Manual of Style (16th Edition):

Gravel, Emilie. “Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance .” 2016. Masters Thesis, Université de Sherbrooke. Accessed October 18, 2019. http://hdl.handle.net/11143/9464.

MLA Handbook (7th Edition):

Gravel, Emilie. “Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance .” 2016. Web. 18 Oct 2019.

Vancouver:

Gravel E. Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance . [Internet] [Masters thesis]. Université de Sherbrooke; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11143/9464.

Council of Science Editors:

Gravel E. Hepsine et matriptase activent l’hémagglutinine des virus influenza A et B et leur inhibition représente une nouvelle stratégie thérapeutique n’entraînant pas le développement de résistance . [Masters Thesis]. Université de Sherbrooke; 2016. Available from: http://hdl.handle.net/11143/9464

16. Zoratti, Gina Lynn. Matriptase Mediated C-Met Signaling In Breast Cancer.

Degree: PhD, Cancer Biology, 2014, Wayne State University

MATRIPTASE MEDIATED c-MET SIGNALING IN CRITICAL FOR BREAST CANCER PROGRESSION by GINA ZORATTI Historically proteases have been associated with tumor progression and metastasis through… (more)

Subjects/Keywords: c-Met; HGF; Matriptase; proteases; Biology; Medicine and Health Sciences

…70 3.13 Matriptase gelatin zymography… …72 4.1 Matriptase hypomorphic mice… …72 4.2 Matriptase conditional knockout mice… …73 Chapter 5: Matriptase mediated c-Met signaling- Results in invasive ductal breast… …mammary carcinomas.................................... 77 5.3 Matriptase hypomorphic mice have… 

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

APA (6th Edition):

Zoratti, G. L. (2014). Matriptase Mediated C-Met Signaling In Breast Cancer. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/949

Chicago Manual of Style (16th Edition):

Zoratti, Gina Lynn. “Matriptase Mediated C-Met Signaling In Breast Cancer.” 2014. Doctoral Dissertation, Wayne State University. Accessed October 18, 2019. https://digitalcommons.wayne.edu/oa_dissertations/949.

MLA Handbook (7th Edition):

Zoratti, Gina Lynn. “Matriptase Mediated C-Met Signaling In Breast Cancer.” 2014. Web. 18 Oct 2019.

Vancouver:

Zoratti GL. Matriptase Mediated C-Met Signaling In Breast Cancer. [Internet] [Doctoral dissertation]. Wayne State University; 2014. [cited 2019 Oct 18]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/949.

Council of Science Editors:

Zoratti GL. Matriptase Mediated C-Met Signaling In Breast Cancer. [Doctoral Dissertation]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_dissertations/949


University of Central Florida

17. Chen, Mengqian. Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer.

Degree: 2007, University of Central Florida

 The glycosylphosphatidylinositol (GPI)-anchored serine protease prostasin (PRSS8) is expressed at the apical membrane surface of epithelial cells and acts as a suppressor of tumor invasion… (more)

Subjects/Keywords: Prostasin; EGFR; prostate cancer; SREBP; Slug; Matriptase; Cancer Biology; Microbiology; Molecular Biology

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

APA (6th Edition):

Chen, M. (2007). Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer. (Doctoral Dissertation). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/3115

Chicago Manual of Style (16th Edition):

Chen, Mengqian. “Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer.” 2007. Doctoral Dissertation, University of Central Florida. Accessed October 18, 2019. https://stars.library.ucf.edu/etd/3115.

MLA Handbook (7th Edition):

Chen, Mengqian. “Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer.” 2007. Web. 18 Oct 2019.

Vancouver:

Chen M. Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer. [Internet] [Doctoral dissertation]. University of Central Florida; 2007. [cited 2019 Oct 18]. Available from: https://stars.library.ucf.edu/etd/3115.

Council of Science Editors:

Chen M. Mechanism Of Action And Regulation Of Membrane Serine Protease Prostasin In The Prostate And Prostate Cancer. [Doctoral Dissertation]. University of Central Florida; 2007. Available from: https://stars.library.ucf.edu/etd/3115

.