141 related articles for article (PubMed ID: 12195424)
21. Processive bidirectional motion of dynein-dynactin complexes in vitro.
Ross JL; Wallace K; Shuman H; Goldman YE; Holzbaur EL
Nat Cell Biol; 2006 Jun; 8(6):562-70. PubMed ID: 16715075
[TBL] [Abstract][Full Text] [Related]
22. Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1.
Smith DS; Niethammer M; Ayala R; Zhou Y; Gambello MJ; Wynshaw-Boris A; Tsai LH
Nat Cell Biol; 2000 Nov; 2(11):767-75. PubMed ID: 11056530
[TBL] [Abstract][Full Text] [Related]
23. Microtubule binding proteins CLIP-170, EB1, and p150Glued form distinct plus-end complexes.
Ligon LA; Shelly SS; Tokito MK; Holzbaur EL
FEBS Lett; 2006 Feb; 580(5):1327-32. PubMed ID: 16455083
[TBL] [Abstract][Full Text] [Related]
24. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.
Tassabehji M
Hum Mol Genet; 2003 Oct; 12 Spec No 2():R229-37. PubMed ID: 12952863
[TBL] [Abstract][Full Text] [Related]
25. Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval.
Zhao C; Avilés C; Abel RA; Almli CR; McQuillen P; Pleasure SJ
Development; 2005 Jun; 132(12):2917-27. PubMed ID: 15930120
[TBL] [Abstract][Full Text] [Related]
26. Metabolic abnormalities in Williams-Beuren syndrome.
Palacios-Verdú MG; Segura-Puimedon M; Borralleras C; Flores R; Del Campo M; Campuzano V; Pérez-Jurado LA
J Med Genet; 2015 Apr; 52(4):248-55. PubMed ID: 25663682
[TBL] [Abstract][Full Text] [Related]
27. Growth defects and impaired cognitive-behavioral abilities in mice with knockout for Eif4h, a gene located in the mouse homolog of the Williams-Beuren syndrome critical region.
Capossela S; Muzio L; Bertolo A; Bianchi V; Dati G; Chaabane L; Godi C; Politi LS; Biffo S; D'Adamo P; Mallamaci A; Pannese M
Am J Pathol; 2012 Mar; 180(3):1121-1135. PubMed ID: 22234171
[TBL] [Abstract][Full Text] [Related]
28. [Dynein and dynactin as organizers of the system of cell microtubules].
Burakov AV; Nadezhdina ES
Ontogenez; 2006; 37(5):323-39. PubMed ID: 17066975
[TBL] [Abstract][Full Text] [Related]
29. Hemizygous deletion of the HPC-1/syntaxin 1A gene (STX1A) in patients with Williams syndrome.
Nakayama T; Matsuoka R; Kimura M; Hirota H; Mikoshiba K; Shimizu Y; Shimizu N; Akagawa K
Cytogenet Cell Genet; 1998; 82(1-2):49-51. PubMed ID: 9763659
[TBL] [Abstract][Full Text] [Related]
30. The membrane-tubulating potential of amphiphysin 2/BIN1 is dependent on the microtubule-binding cytoplasmic linker protein 170 (CLIP-170).
Meunier B; Quaranta M; Daviet L; Hatzoglou A; Leprince C
Eur J Cell Biol; 2009 Feb; 88(2):91-102. PubMed ID: 19004523
[TBL] [Abstract][Full Text] [Related]
31. Function of dynein and dynactin in herpes simplex virus capsid transport.
Döhner K; Wolfstein A; Prank U; Echeverri C; Dujardin D; Vallee R; Sodeik B
Mol Biol Cell; 2002 Aug; 13(8):2795-809. PubMed ID: 12181347
[TBL] [Abstract][Full Text] [Related]
32. Chlamydia trachomatis uses host cell dynein to traffic to the microtubule-organizing center in a p50 dynamitin-independent process.
Grieshaber SS; Grieshaber NA; Hackstadt T
J Cell Sci; 2003 Sep; 116(Pt 18):3793-802. PubMed ID: 12902405
[TBL] [Abstract][Full Text] [Related]
33. The role of the lissencephaly protein Pac1 during nuclear migration in budding yeast.
Lee WL; Oberle JR; Cooper JA
J Cell Biol; 2003 Feb; 160(3):355-64. PubMed ID: 12566428
[TBL] [Abstract][Full Text] [Related]
34. A motor neuron disease-associated mutation in p150Glued perturbs dynactin function and induces protein aggregation.
Levy JR; Sumner CJ; Caviston JP; Tokito MK; Ranganathan S; Ligon LA; Wallace KE; LaMonte BH; Harmison GG; Puls I; Fischbeck KH; Holzbaur EL
J Cell Biol; 2006 Feb; 172(5):733-45. PubMed ID: 16505168
[TBL] [Abstract][Full Text] [Related]
35. A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function.
Faulkner NE; Dujardin DL; Tai CY; Vaughan KT; O'Connell CB; Wang Y; Vallee RB
Nat Cell Biol; 2000 Nov; 2(11):784-91. PubMed ID: 11056532
[TBL] [Abstract][Full Text] [Related]
36. Cytoplasmic dynein mediates adenovirus binding to microtubules.
Kelkar SA; Pfister KK; Crystal RG; Leopold PL
J Virol; 2004 Sep; 78(18):10122-32. PubMed ID: 15331745
[TBL] [Abstract][Full Text] [Related]
37. Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
DeSilva U; Elnitski L; Idol JR; Doyle JL; Gan W; Thomas JW; Schwartz S; Dietrich NL; Beckstrom-Sternberg SM; McDowell JC; Blakesley RW; Bouffard GG; Thomas PJ; Touchman JW; Miller W; Green ED
Genome Res; 2002 Jan; 12(1):3-15. PubMed ID: 11779826
[TBL] [Abstract][Full Text] [Related]
38. The Williams syndrome cognitive profile.
Mervis CB; Robinson BF; Bertrand J; Morris CA; Klein-Tasman BP; Armstrong SC
Brain Cogn; 2000 Dec; 44(3):604-28. PubMed ID: 11104544
[TBL] [Abstract][Full Text] [Related]
39. Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
Durkin ME; Keck-Waggoner CL; Popescu NC; Thorgeirsson SS
Genomics; 2001 Apr; 73(1):20-7. PubMed ID: 11352562
[TBL] [Abstract][Full Text] [Related]
40. BAZ1B is a candidate gene responsible for hypothyroidism in Williams syndrome.
Allegri L; Baldan F; Mio C; De Felice M; Amendola E; Damante G
Eur J Med Genet; 2020 Jun; 63(6):103894. PubMed ID: 32081709
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
