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93 results for PSTPIP1

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Select record 21
ArticlesPeer ReviewedFull Text
Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient and relevance to the PSTPIP1 gene
Author / Creator:Lin, Zhenwu ; Hegarty, John P. ; Lin, Tony ; Ostrov, Barbara ; Wang, Yunhua ; Yu, Wei ; Kelly, Ashley A. ; Poritz, Lisa S. ; Koltun, Walter A.
Publisher:Oxford, UK: Oxford University Press
Journal title:Inflammatory bowel diseases, 2011-06, Vol.17 (6), p.E41-E42
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ArticlesPeer ReviewedFull Text
Longest Form of CCTG Microsatellite Repeat in the Promoter of the CD2BP1/PSTPIP1 Gene Is Associated with Aseptic Abscesses and with Crohn Disease in French Patients
Author / Creator:André, Marc F. J ; Aumaître, Olivier ; Grateau, Gilles ; Chamaillard, Mathias ; Costedoat-Chalumeau, Nathalie ; Cardoso, Marie-Céleste ; Henry-Berger, Joëlle ; Ramakrishna, Balakrishnan S ; Delpech, Marc ; Piette, Jean-Charles ; Creveaux, Isabelle
Publisher:Boston: Boston : Springer US
Journal title:Digestive diseases and sciences, 2010-06, Vol.55 (6), p.1681-1688
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ArticlesPeer ReviewedFull Text
PW01-001 – Pyrin-PSTPIP1 relation during cell migration
Author / Creator:Akkaya, ZY ; Balci-Peynircioglu, B ; Cetinkaya, A ; Purali, N ; Yilmaz, E
Publisher:BioMed Central
Journal title:Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A54-A54, Article A54
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ArticlesPeer ReviewedFull Text
PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype
Author / Creator:Holzinger, D ; Lohse, P ; Faßl, S ; Austermann, J ; Vogl, T ; de Jager, W ; Holland, S ; Gattorno, M ; Rodriguez-Gallego, C ; Arostegui, J ; Fessatou, S ; Isidor, B ; Ito, K ; Epple, H-J ; Bernstein, J ; Jeng, M ; Lionetti, G ; Ong, P ; Hinze, C ; Sampson, B ; Sunderkoetter, C ; Foell, D ; Chae, J ; Ombrello, A ; Brady, J ; Aksentijevich, I ; Roth, J
Publisher:Springer Science and Business Media LLC
Journal title:Pediatric Rheumatology, 2013-11, Vol.11 (S1), p.A158-A158, Article A158
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ArticlesPeer ReviewedFull Text
P02-006 - A novel PSTPIP1 mutation in PAPA syndrome
Author / Creator:Fathalla, B ; Al-Mutawa, M ; Al-Amri, F ; Al-Dosari, S ; Kambouris, M ; El-Shanti, H
Publisher:London: BioMed Central
Journal title:Pediatric Rheumatology, 2013-11, Vol.11 (S1), p.A113-A113, Article A113
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ArticlesPeer ReviewedFull Text
P02-018 - PSTPIP1 gene mutations in periodic fever patients
Author / Creator:Takabe, K ; Adachi, Y ; Saito, H ; Yamashita, T ; Wakai, Y ; Saito, K ; Shinohara, Y
Publisher:BioMed Central
Journal title:Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A125-A125, Article A125
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ArticlesPeer ReviewedFull Text
Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient with microsatellite variation in the promoter region of the PSTPIP1 gene: P-135
Author / Creator:Lin, Z ; Hegarty, J ; Lin, T ; Lin, Y ; Ostrov, B ; Kelly, A ; Poritz, L ; Koltun, W
Publisher:Baltimore: Oxford University Press
Journal title:Inflammatory bowel diseases, 2011-01, Vol.17, p.S52-S52
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ArticlesPeer ReviewedFull Text
Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient with microsatellite variation in the promoter region of the PSTPIP1 gene
Author / Creator:Lin, Z ; Hegarty, J ; Lin, T ; Lin, Y ; Ostrov, B ; Kelly, A ; Poritz, L ; Koltun, W
Publisher:Oxford, UK: Oxford University Press
Journal title:Inflammatory bowel diseases, 2011-01, Vol.17 (suppl_1), p.S52-S52
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ArticlesPeer ReviewedFull Text
PSTPIP1-LYP phosphatase interaction: structural basis and implications for autoinflammatory disorders
Publisher:Basel: Springer Nature B.V
Journal title:Cellular and molecular life sciences : CMLS, 2022-02, Vol.79 (2), p.131
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ArticlesPeer ReviewedFull Text
A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome
Author / Creator:Holzinger, D ; Austermann, J ; Lohse, P ; Aksentijevich, I ; Holland, S ; Gattorno, M ; Rodríguez-Gallego, C ; Fessatou, S ; Isidor, B ; Tokio, S ; Bernstein, J ; Sampson, B ; Sunderkoetter, C ; Roth, J
Publisher:London: BioMed Central
Journal title:Pediatric Rheumatology, 2011-09, Vol.9 (S1), p.O39-O39, Article O39
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ArticlesPeer ReviewedFull Text
PSTPIP1-associated myeloid-related proteinaemia inflammatory (PAMI) syndrome; a case presenting as a perinatal event with early central nervous system involvement?
Author / Creator:Whiteside, Bethany Gillies ; Titheradge, Hannah ; Al-Abadi, Eslam
Publisher:England: BioMed Central Ltd
Journal title:Pediatric Rheumatology, 2022-07, Vol.20 (1), p.49-9, Article 49
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ArticlesPeer ReviewedFull Text
Infevers: An evolving mutation database for auto-inflammatory syndromes
Author / Creator:Touitou, Isabelle ; Lesage, Suzanne ; McDermott, Michael ; Cuisset, Laurence ; Hoffman, Hal ; Dode, Catherine ; Shoham, Nitza ; Aganna, Ebun ; Hugot, Jean-Pierre ; Wise, Carol ; Waterham, Hans ; Pugnere, Denis ; Demaille, Jacques ; de Menthiere, Cyril Sarrauste
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2004-09, Vol.24 (3), p.194-198
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ArticlesFull Text
PTPN22 Regulates T Cell Synapse Formation through PSTPIP1- Dependent Actin Remodeling
Author / Creator:Joseph, Megan D. ; Zaza, Cecilia ; Dalby, Olivia P. L. ; Dustin, Michael L. ; Cope, Andrew P. ; Simoncelli, Sabrina
Publisher:Cold Spring Harbor Laboratory
Journal title:bioRxiv, 2025-04
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ArticlesPeer ReviewedFull Text
PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review
Author / Creator:Mejbri, Manel ; Renella, Raffaele ; Candotti, Fabio ; Jaques, Cecile ; Holzinger, Dirk ; Hofer, Michael ; Theodoropoulou, Katerina
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-08, Vol.14 (8), p.1655
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Newsletter articlesFull Text
Excess Serum Interleukin-18 Distinguishes Patients with Pathogenic Mutations in PSTPIP1
Publisher:NewsRX LLC
Journal title:Health & Medicine Week, 2021, p.2345
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Newsletter articlesFull Text
Rare missense variants in the SH3 domain of PSTPIP1 are associated with hidradenitis suppurativa
Publisher:NewsRX LLC
Journal title:Health & Medicine Week, 2022, p.4570
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ArticlesPeer ReviewedFull Text
Autoinflammatory gene mutations in Behçet’s disease
Author / Creator:Koné-Paut, I ; Sanchez, E ; Le Quellec, A ; Manna, R ; Touitou, I
Publisher:London: BMJ Publishing Group Ltd and European League Against Rheumatism
Journal title:Annals of the rheumatic diseases, 2007-06, Vol.66 (6), p.832-834
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Newsletter articlesFull Text
Study Findings from Foshan Advance Knowledge in COVID-19 (Stimulation of PSTPIP1 to trigger proinflammatory responses in asymptomatic SARS-CoV-2 infections)
Publisher:NewsRX LLC
Journal title:Respiratory Therapeutics Week, 2024, p.673
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A very rare cause of pre‐capillary pulmonary hypertension: The PAMI syndrome
Author / Creator:Iseppi, Manuela ; Savonitto, Giulio ; Tommasini, Alberto ; Pin, Alessia ; Sinagra, Gianfranco ; Stolfo, Davide
Publisher:United States: John Wiley & Sons, Inc
Journal title:PULMONARY CIRCULATION, 2023-10, Vol.13 (4), p.e12300-n/a
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Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts
Author / Creator:Löffler, W. ; Lohse, P. ; Weihmayr, T. ; Widenmayer, W.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Infection, 2017-08, Vol.45 (4), p.395-402
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Showing 21 to 40 of 93 results

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Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient and relevance to the PSTPIP1 gene

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Longest Form of CCTG Microsatellite Repeat in the Promoter of the CD2BP1/PSTPIP1 Gene Is Associated with Aseptic Abscesses and with Crohn Disease in French Patients

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PW01-001 – Pyrin-PSTPIP1 relation during cell migration

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PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype

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P02-006 - A novel PSTPIP1 mutation in PAPA syndrome

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P02-018 - PSTPIP1 gene mutations in periodic fever patients

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Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient with microsatellite variation in the promoter region of the PSTPIP1 gene: P-135

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Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient with microsatellite variation in the promoter region of the PSTPIP1 gene

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PSTPIP1-LYP phosphatase interaction: structural basis and implications for autoinflammatory disorders

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A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome

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PSTPIP1-associated myeloid-related proteinaemia inflammatory (PAMI) syndrome; a case presenting as a perinatal event with early central nervous system involvement?

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Infevers: An evolving mutation database for auto-inflammatory syndromes

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PTPN22 Regulates T Cell Synapse Formation through PSTPIP1- Dependent Actin Remodeling

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PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review

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Excess Serum Interleukin-18 Distinguishes Patients with Pathogenic Mutations in PSTPIP1

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Rare missense variants in the SH3 domain of PSTPIP1 are associated with hidradenitis suppurativa

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Autoinflammatory gene mutations in Behçet’s disease

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Study Findings from Foshan Advance Knowledge in COVID-19 (Stimulation of PSTPIP1 to trigger proinflammatory responses in asymptomatic SARS-CoV-2 infections)

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A very rare cause of pre‐capillary pulmonary hypertension: The PAMI syndrome

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Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts

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