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Items: 18

1.

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

Münch C, Sedlmeier R, Meyer T, Homberg V, Sperfeld AD, Kurt A, Prudlo J, Peraus G, Hanemann CO, Stumm G, Ludolph AC.

Neurology. 2004 Aug 24;63(4):724-6.

PMID:
15326253
2.

Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules.

Gauthier LR, Charrin BC, Borrell-Pagès M, Dompierre JP, Rangone H, Cordelières FP, De Mey J, MacDonald ME, Lessmann V, Humbert S, Saudou F.

Cell. 2004 Jul 9;118(1):127-38.

3.

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.

Kim JC, Badano JL, Sibold S, Esmail MA, Hill J, Hoskins BE, Leitch CC, Venner K, Ansley SJ, Ross AJ, Leroux MR, Katsanis N, Beales PL.

Nat Genet. 2004 May;36(5):462-70. Epub 2004 Apr 25.

PMID:
15107855
4.

Mutant dynactin in motor neuron disease.

Puls I, Jonnakuty C, LaMonte BH, Holzbaur EL, Tokito M, Mann E, Floeter MK, Bidus K, Drayna D, Oh SJ, Brown RH Jr, Ludlow CL, Fischbeck KH.

Nat Genet. 2003 Apr;33(4):455-6. Epub 2003 Mar 10.

PMID:
12627231
5.

Genomic organization of the DCTN1-SLC4A5 locus encoding both NBC4 and p150(Glued).

Pushkin A, Abuladze N, Newman D, Tatishchev S, Kurtz I.

Cytogenet Cell Genet. 2001;95(3-4):163-8.

PMID:
12063394
6.

Dynactin is necessary for synapse stabilization.

Eaton BA, Fetter RD, Davis GW.

Neuron. 2002 May 30;34(5):729-41.

7.

Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.

LaMonte BH, Wallace KE, Holloway BA, Shelly SS, Ascaño J, Tokito M, Van Winkle T, Howland DS, Holzbaur EL.

Neuron. 2002 May 30;34(5):715-27.

8.

Japanese family with parkinsonism, depression, weight loss, and central hypoventilation.

Tsuboi Y, Wszolek ZK, Kusuhara T, Doh-ura K, Yamada T.

Neurology. 2002 Apr 9;58(7):1025-30.

PMID:
11940687
9.

Human DCTN1: genomic structure and evaluation as a candidate for Alström syndrome.

Collin GB, Nishina PM, Marshall JD, Naggert JK.

Genomics. 1998 Nov 1;53(3):359-64.

PMID:
9799602
10.

Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases.

Korthaus D, Wedemeyer N, Lengeling A, Ronsiek M, Jockusch H, Schmitt-John T.

Genomics. 1997 Jul 15;43(2):242-4.

PMID:
9244444
11.

Mouse p150Glued (dynactin 1) cDNA sequence and evaluation as a candidate for the neuromuscular disease mutation mnd2.

Jang W, Weber JS, Tokito MK, Holzbaur EL, Meisler MH.

Biochem Biophys Res Commun. 1997 Feb 13;231(2):344-7.

PMID:
9070275
12.

Localization of the DCTN1 gene encoding p150Glued to human chromosome 2p13 by fluorescence in situ hybridization.

Holzbaur EL, Tokito MK.

Genomics. 1996 Feb 1;31(3):398-9. No abstract available.

PMID:
8838327
13.

DYNEINS: molecular structure and cellular function.

Holzbaur EL, Vallee RB.

Annu Rev Cell Biol. 1994;10:339-72. Review. No abstract available.

PMID:
7888180
14.

Familial parkinsonism, apathy, weight loss, and central hypoventilation: successful long-term management.

Roy EP 3rd, Riggs JE, Martin JD, Ringel RA, Gutmann L.

Neurology. 1988 Apr;38(4):637-9.

PMID:
3352925
15.
16.

[Familial parkinsonian syndrome with athymhormia and hypoventilation].

Lechevalier B, Schupp C, Fallet-Bianco C, Viader F, Eustache F, Chapon F, Morin P.

Rev Neurol (Paris). 1992;148(1):39-46. Review. French.

PMID:
1604112
17.

Hereditary mental depression and Parkinsonism with taurine deficiency.

Perry TL, Bratty PJ, Hansen S, Kennedy J, Urquhart N, Dolman CL.

Arch Neurol. 1975 Feb;32(2):108-13.

PMID:
1122173
18.

Familial fatal Parkinsonism with alveolar hypoventilation and mental depression.

Purdy A, Hahn A, Barnett HJ, Bratty P, Ahmad D, Lloyd KG, McGeer EG, Perry TL.

Ann Neurol. 1979 Dec;6(6):523-31.

PMID:
43704

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