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6. The Phenotypic Spectrum of PNKP-Associated Disease and the Absence of Immunodeficiency and Cancer Predisposition in a Dutch Cohort. Garrelfs MR; Takada S; Kamsteeg EJ; Pegge S; Mancini G; Engelen M; van de Warrenburg B; Rennings A; van Gaalen J; Peters I; Weemaes C; van der Burg M; Willemsen MA Pediatr Neurol; 2020 Dec; 113():26-32. PubMed ID: 32980744 [TBL] [Abstract][Full Text] [Related]
7. Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair. Kalasova I; Hailstone R; Bublitz J; Bogantes J; Hofmann W; Leal A; Hanzlikova H; Caldecott KW Nucleic Acids Res; 2020 Jul; 48(12):6672-6684. PubMed ID: 32504494 [TBL] [Abstract][Full Text] [Related]
8. Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Shen J; Gilmore EC; Marshall CA; Haddadin M; Reynolds JJ; Eyaid W; Bodell A; Barry B; Gleason D; Allen K; Ganesh VS; Chang BS; Grix A; Hill RS; Topcu M; Caldecott KW; Barkovich AJ; Walsh CA Nat Genet; 2010 Mar; 42(3):245-9. PubMed ID: 20118933 [TBL] [Abstract][Full Text] [Related]
9. Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia. da Costa SCG; Rezende Filho FM; de Freitas JL; de Assis Pereira Matos PCA; Della-Ripa B; França MC; Marques W; Santos M; Cronemberger IVB; Vale TC; Kok F; Alonso I; Pedroso JL; Barsottini OGP Mov Disord; 2022 Jun; 37(6):1309-1316. PubMed ID: 35426160 [TBL] [Abstract][Full Text] [Related]
10. Pitfalls in ataxia with ocular motor apraxia type 1: pseudodominant inheritance and very late onset. Laurencin C; Anheim M; Larrieu L; Tilikete C; Koenig M; Thobois S J Neurol; 2015 May; 262(5):1366-8. PubMed ID: 25845762 [No Abstract] [Full Text] [Related]
11. From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations. Gatti M; Magri S; Nanetti L; Sarto E; Di Bella D; Salsano E; Pantaleoni C; Mariotti C; Taroni F Am J Med Genet A; 2019 Nov; 179(11):2277-2283. PubMed ID: 31436889 [TBL] [Abstract][Full Text] [Related]
12. Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing loss. Nakashima M; Takano K; Osaka H; Aida N; Tsurusaki Y; Miyake N; Saitsu H; Matsumoto N J Hum Genet; 2014 Aug; 59(8):471-4. PubMed ID: 24965255 [TBL] [Abstract][Full Text] [Related]
13. Exploring the Pathogenicity of SETX I1942T Variant in Ataxia with Oculomotor Apraxia Type 2 Through Segregation Analysis. Ros-Arlanzón P; Serrano-Serrano B; Aledo-Sala C; Guevara-Dalrymple N; Martí-Martínez S Mov Disord Clin Pract; 2024 Aug; 11(8):1041-1043. PubMed ID: 38817201 [No Abstract] [Full Text] [Related]
14. Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1. Renaud M; Moreira MC; Ben Monga B; Rodriguez D; Debs R; Charles P; Chaouch M; Ferrat F; Laurencin C; Vercueil L; Mallaret M; M'Zahem A; Pacha LA; Tazir M; Tilikete C; Ollagnon E; Ochsner F; Kuntzer T; Jung HH; Beis JM; Netter JC; Djamshidian A; Bower M; Bottani A; Walsh R; Murphy S; Reiley T; Bieth É; Roelens F; Poll-The BT; Lourenço CM; Jardim LB; Straussberg R; Landrieu P; Roze E; Thobois S; Pouget J; Guissart C; Goizet C; Dürr A; Tranchant C; Koenig M; Anheim M JAMA Neurol; 2018 Apr; 75(4):495-502. PubMed ID: 29356829 [TBL] [Abstract][Full Text] [Related]
15. XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia. Hoch NC; Hanzlikova H; Rulten SL; Tétreault M; Komulainen E; Ju L; Hornyak P; Zeng Z; Gittens W; Rey SA; Staras K; Mancini GM; McKinnon PJ; Wang ZQ; Wagner JD; ; Yoon G; Caldecott KW Nature; 2017 Jan; 541(7635):87-91. PubMed ID: 28002403 [TBL] [Abstract][Full Text] [Related]
16. Compound Heterozygous Mutations in Bitarafan F; Khodaeian M; Almadani N; Kalhor A; Sardehaei EA; Garshasbi M Fetal Pediatr Pathol; 2021 Apr; 40(2):174-180. PubMed ID: 31707899 [TBL] [Abstract][Full Text] [Related]
17. Oculomotor apraxia in Gaucher disease. Nagappa M; Bindu PS; Taly AB; Sinha S Pediatr Neurol; 2015 Apr; 52(4):468-9. PubMed ID: 25687160 [No Abstract] [Full Text] [Related]
18. Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation. Nair P; Hamzeh AR; Mohamed M; Saif F; Tawfiq N; El Halik M; Al-Ali MT; Bastaki F Am J Med Genet A; 2016 Aug; 170(8):2127-32. PubMed ID: 27232581 [TBL] [Abstract][Full Text] [Related]
19. Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair. Reynolds JJ; Walker AK; Gilmore EC; Walsh CA; Caldecott KW Nucleic Acids Res; 2012 Aug; 40(14):6608-19. PubMed ID: 22508754 [TBL] [Abstract][Full Text] [Related]
20. Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation. Entezam M; Razipour M; Talebi S; Beiraghi Toosi M; Keramatipour M Brain Dev; 2019 Feb; 41(2):182-186. PubMed ID: 30195441 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]