These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
505 related articles for article (PubMed ID: 15793586)
1. A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Bond J; Roberts E; Springell K; Lizarraga SB; Scott S; Higgins J; Hampshire DJ; Morrison EE; Leal GF; Silva EO; Costa SM; Baralle D; Raponi M; Karbani G; Rashid Y; Jafri H; Bennett C; Corry P; Walsh CA; Woods CG Nat Genet; 2005 Apr; 37(4):353-5. PubMed ID: 15793586 [TBL] [Abstract][Full Text] [Related]
2. CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly. Sukumaran SK; Stumpf M; Salamon S; Ahmad I; Bhattacharya K; Fischer S; Müller R; Altmüller J; Budde B; Thiele H; Tariq M; Malik NA; Nürnberg P; Baig SM; Hussain MS; Noegel AA Mol Genet Genomics; 2017 Apr; 292(2):365-383. PubMed ID: 28004182 [TBL] [Abstract][Full Text] [Related]
5. Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. Kumar A; Girimaji SC; Duvvari MR; Blanton SH Am J Hum Genet; 2009 Feb; 84(2):286-90. PubMed ID: 19215732 [TBL] [Abstract][Full Text] [Related]
6. Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. Issa L; Mueller K; Seufert K; Kraemer N; Rosenkotter H; Ninnemann O; Buob M; Kaindl AM; Morris-Rosendahl DJ Orphanet J Rare Dis; 2013 Apr; 8():59. PubMed ID: 23587236 [TBL] [Abstract][Full Text] [Related]
7. Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disability. Saima ; Khan A; Ali S; Jiang J; Miao Z; Kamil A; Khan SN; Arold ST Neurogenetics; 2024 Jul; 25(3):179-191. PubMed ID: 38795246 [TBL] [Abstract][Full Text] [Related]
8. What primary microcephaly can tell us about brain growth. Cox J; Jackson AP; Bond J; Woods CG Trends Mol Med; 2006 Aug; 12(8):358-66. PubMed ID: 16829198 [TBL] [Abstract][Full Text] [Related]
9. An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan. Rasool S; Baig JM; Moawia A; Ahmad I; Iqbal M; Waseem SS; Asif M; Abdullah U; Makhdoom EUH; Kaygusuz E; Zakaria M; Ramzan S; Haque SU; Mir A; Anjum I; Fiaz M; Ali Z; Tariq M; Saba N; Hussain W; Budde B; Irshad S; Noegel AA; Höning S; Baig SM; Nürnberg P; Hussain MS Mol Genet Genomic Med; 2020 Sep; 8(9):e1408. PubMed ID: 32677750 [TBL] [Abstract][Full Text] [Related]
10. CDK5RAP2 functions in centrosome to spindle pole attachment and DNA damage response. Barr AR; Kilmartin JV; Gergely F J Cell Biol; 2010 Apr; 189(1):23-39. PubMed ID: 20368616 [TBL] [Abstract][Full Text] [Related]
11. Molecular evolution of the brain size regulator genes CDK5RAP2 and CENPJ. Evans PD; Vallender EJ; Lahn BT Gene; 2006 Jun; 375():75-9. PubMed ID: 16631324 [TBL] [Abstract][Full Text] [Related]
12. Primary microcephaly 3 (MCPH3): revisiting two critical mutations. Park JS; Lee MK; Rosales JL; Lee KY Cell Cycle; 2011 Apr; 10(8):1331-3. PubMed ID: 21512315 [No Abstract] [Full Text] [Related]
13. WDR62 is associated with the spindle pole and is mutated in human microcephaly. Nicholas AK; Khurshid M; Désir J; Carvalho OP; Cox JJ; Thornton G; Kausar R; Ansar M; Ahmad W; Verloes A; Passemard S; Misson JP; Lindsay S; Gergely F; Dobyns WB; Roberts E; Abramowicz M; Woods CG Nat Genet; 2010 Nov; 42(11):1010-4. PubMed ID: 20890279 [TBL] [Abstract][Full Text] [Related]
14. Molecular and cellular basis of autosomal recessive primary microcephaly. Barbelanne M; Tsang WY Biomed Res Int; 2014; 2014():547986. PubMed ID: 25548773 [TBL] [Abstract][Full Text] [Related]
15. CEP215 is involved in the dynein-dependent accumulation of pericentriolar matrix proteins for spindle pole formation. Lee S; Rhee K Cell Cycle; 2010 Feb; 9(4):774-83. PubMed ID: 20139723 [TBL] [Abstract][Full Text] [Related]
16. Human microcephaly ASPM protein is a spindle pole-focusing factor that functions redundantly with CDK5RAP2. Tungadi EA; Ito A; Kiyomitsu T; Goshima G J Cell Sci; 2017 Nov; 130(21):3676-3684. PubMed ID: 28883092 [TBL] [Abstract][Full Text] [Related]
17. The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis. Bakircioglu M; Carvalho OP; Khurshid M; Cox JJ; Tuysuz B; Barak T; Yilmaz S; Caglayan O; Dincer A; Nicholas AK; Quarrell O; Springell K; Karbani G; Malik S; Gannon C; Sheridan E; Crosier M; Lisgo SN; Lindsay S; Bilguvar K; Gergely F; Gunel M; Woods CG Am J Hum Genet; 2011 May; 88(5):523-35. PubMed ID: 21529752 [TBL] [Abstract][Full Text] [Related]