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Showing results for peter loken
Your search for Peter Locken retrieved no results
Multiparameter flow cytometry in the evaluation of myelodysplasia: Analytical issues: Recommendations from the European LeukemiaNet/International Myelodysplastic Syndrome Flow Cytometry Working Group.
Porwit A, Béné MC, Duetz C, Matarraz S, Oelschlaegel U, Westers TM, Wagner-Ballon O, Kordasti S, Valent P, Preijers F, Alhan C, Bellos F, Bettelheim P, Burbury K, Chapuis N, Cremers E, Della Porta MG, Dunlop A, Eidenschink-Brodersen L, Font P, Fontenay M, Hobo W, Ireland R, Johansson U, Loken MR, Ogata K, Orfao A, Psarra K, Saft L, Subira D, Te Marvelde J, Wells DA, van der Velden VHJ, Kern W, van de Loosdrecht AA. Porwit A, et al. Cytometry B Clin Cytom. 2023 Jan;104(1):27-50. doi: 10.1002/cyto.b.22108. Epub 2022 Dec 20. Cytometry B Clin Cytom. 2023. PMID: 36537621 Free PMC article. Review.
Genetic complexity in Joubert syndrome and related disorders.
Harris PC. Harris PC. Kidney Int. 2007 Dec;72(12):1421-3. doi: 10.1038/sj.ki.5002577. Kidney Int. 2007. PMID: 18046420 Free article. Review.
Three of these are also associated with the lethal Meckel syndrome, and two with Senior-Loken syndrome; both of these disorders share Joubert syndrome phenotypes, illustrating the genetic complexity of this....
Three of these are also associated with the lethal Meckel syndrome, and two with Senior-Loken syndrome; both of these disorders share …
Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Loken syndrome?
Vogel P, Gelfman CM, Issa T, Payne BJ, Hansen GM, Read RW, Jones C, Pitcher MR, Ding ZM, DaCosta CM, Shadoan MK, Vance RB, Powell DR. Vogel P, et al. Vet Pathol. 2015 May;52(3):580-95. doi: 10.1177/0300985814547392. Epub 2014 Aug 26. Vet Pathol. 2015. PMID: 25161209
At least 10% of NPHP cases present with extrarenal conditions, which most often include retinal degeneration. Senior-Loken syndrome is characterized by the concurrent development of autosomal recessive NPHP and retinitis pigmentosa. ...In reviewing all other reported mouse …
At least 10% of NPHP cases present with extrarenal conditions, which most often include retinal degeneration. Senior-Loken syndrome i …
Definitions and standards in the diagnosis and treatment of the myelodysplastic syndromes: Consensus statements and report from a working conference.
Valent P, Horny HP, Bennett JM, Fonatsch C, Germing U, Greenberg P, Haferlach T, Haase D, Kolb HJ, Krieger O, Loken M, van de Loosdrecht A, Ogata K, Orfao A, Pfeilstöcker M, Rüter B, Sperr WR, Stauder R, Wells DA. Valent P, et al. Leuk Res. 2007 Jun;31(6):727-36. doi: 10.1016/j.leukres.2006.11.009. Epub 2007 Jan 25. Leuk Res. 2007. PMID: 17257673 Review.
Genetic profile of syndromic retinitis pigmentosa in Portugal.
Cortinhal T, Santos C, Vaz-Pereira S, Marta A, Duarte L, Miranda V, Costa J, Sousa AB, Peter VG, Kaminska K, Rivolta C, Carvalho AL, Saraiva J, Soares CA, Silva R, Murta J, Santos LC, Marques JP. Cortinhal T, et al. Graefes Arch Clin Exp Ophthalmol. 2024 Jun;262(6):1883-1897. doi: 10.1007/s00417-023-06360-2. Epub 2024 Jan 8. Graefes Arch Clin Exp Ophthalmol. 2024. PMID: 38189974 Free PMC article.
Usher syndrome was the most frequent diagnosis (62.0%), followed by Bardet-Biedl (19.0%) and Senior-Loken syndromes (7.0%). Deleterious variants were identified in 86/100 families for a diagnostic yield of 86.0% (87.1% for Usher and 94.7% for Bardet-Biedl). ...
Usher syndrome was the most frequent diagnosis (62.0%), followed by Bardet-Biedl (19.0%) and Senior-Loken syndromes (7.0%). Deleterio …
Flow cytometric analysis of myelodysplasia: Pre-analytical and technical issues-Recommendations from the European LeukemiaNet.
van der Velden VHJ, Preijers F, Johansson U, Westers TM, Dunlop A, Porwit A, Béné MC, Valent P, Te Marvelde J, Wagner-Ballon O, Oelschlaegel U, Saft L, Kordasti S, Ireland R, Cremers E, Alhan C, Duetz C, Hobo W, Chapuis N, Fontenay M, Bettelheim P, Eidenshink-Brodersen L, Font P, Loken MR, Matarraz S, Ogata K, Orfao A, Psarra K, Subirá D, Wells DA, Della Porta MG, Burbury K, Bellos F, Weiß E, Kern W, van de Loosdrecht A. van der Velden VHJ, et al. Cytometry B Clin Cytom. 2023 Jan;104(1):15-26. doi: 10.1002/cyto.b.22046. Epub 2021 Dec 11. Cytometry B Clin Cytom. 2023. PMID: 34894176 Free PMC article.
"Context-dependent learning in social interaction: Trait impressions support flexible social choices": Correction to Hackel et al. (2022).
[No authors listed] [No authors listed] J Pers Soc Psychol. 2022 Oct;123(4):675. doi: 10.1037/pspa0000325. J Pers Soc Psychol. 2022. PMID: 36136778
Reports an error in "Context-dependent learning in social interaction: Trait impressions support flexible social choices" by Leor M. Hackel, Peter Mende-Siedlecki, Siri Loken and David M. Amodio (Journal of Personality and Social Psychology, Advanced Online Publicat …
Reports an error in "Context-dependent learning in social interaction: Trait impressions support flexible social choices" by Leor M. Hackel, …
Clinical application of flow cytometry in patients with unexplained cytopenia and suspected myelodysplastic syndrome: A report of the European LeukemiaNet International MDS-Flow Cytometry Working Group.
van de Loosdrecht AA, Kern W, Porwit A, Valent P, Kordasti S, Cremers E, Alhan C, Duetz C, Dunlop A, Hobo W, Preijers F, Wagner-Ballon O, Chapuis N, Fontenay M, Bettelheim P, Eidenschink-Brodersen L, Font P, Johansson U, Loken MR, Te Marvelde JG, Matarraz S, Ogata K, Oelschlaegel U, Orfao A, Psarra K, Subirá D, Wells DA, Béné MC, Della Porta MG, Burbury K, Bellos F, van der Velden VHJ, Westers TM, Saft L, Ireland R. van de Loosdrecht AA, et al. Cytometry B Clin Cytom. 2023 Jan;104(1):77-86. doi: 10.1002/cyto.b.22044. Epub 2021 Dec 13. Cytometry B Clin Cytom. 2023. PMID: 34897979 Free article.
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Märker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R. Arts HH, et al. Nat Genet. 2007 Jul;39(7):882-8. doi: 10.1038/ng2069. Epub 2007 Jun 10. Nat Genet. 2007. PMID: 17558407
Protein-protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronophthisis (NPHP), Leber congenital amaurosis, Senior-Loken syndrome (SLSN) or Joubert syndrome (JBTS). However, details of the molecular …
Protein-protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronopht …
37 results