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Items: 1 to 20 of 126

1.

The murine tub (rd5) mutation is not associated with a primary axonemal defect.

Ohlemiller KK, Mosinger Ogilvie J, Lett JM, Hughes RM, LaRegina MC, Olson LM.

Cell Tissue Res. 1998 Mar;291(3):489-95.

PMID:
9477305
2.

Cochlear and retinal degeneration in the tubby mouse.

Ohlemiller KK, Hughes RM, Mosinger-Ogilvie J, Speck JD, Grosof DH, Silverman MS.

Neuroreport. 1995 Apr 19;6(6):845-9.

PMID:
7612867
3.

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene.

Ikeda S, Shiva N, Ikeda A, Smith RS, Nusinowitz S, Yan G, Lin TR, Chu S, Heckenlively JR, North MA, Naggert JK, Nishina PM, Duyao MP.

Hum Mol Genet. 2000 Jan 22;9(2):155-63.

PMID:
10607826
4.

Genetic modification of retinal degeneration in tubby mice.

Ikeda A, Naggert JK, Nishina PM.

Exp Eye Res. 2002 Apr;74(4):455-61.

PMID:
12076089
5.

Targeted deletion of the tub mouse obesity gene reveals that tubby is a loss-of-function mutation.

Stubdal H, Lynch CA, Moriarty A, Fang Q, Chickering T, Deeds JD, Fairchild-Huntress V, Charlat O, Dunmore JH, Kleyn P, Huszar D, Kapeller R.

Mol Cell Biol. 2000 Feb;20(3):878-82.

6.

Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome.

Fath MA, Mullins RF, Searby C, Nishimura DY, Wei J, Rahmouni K, Davis RE, Tayeh MK, Andrews M, Yang B, Sigmund CD, Stone EM, Sheffield VC.

Hum Mol Genet. 2005 May 1;14(9):1109-18. Epub 2005 Mar 16.

PMID:
15772095
7.

Abnormal sperm and photoreceptor axonemes in Usher's syndrome.

Hunter DG, Fishman GA, Mehta RS, Kretzer FL.

Arch Ophthalmol. 1986 Mar;104(3):385-9.

PMID:
3954639
8.

Defective carbohydrate metabolism in mice homozygous for the tubby mutation.

Wang Y, Seburn K, Bechtel L, Lee BY, Szatkiewicz JP, Nishina PM, Naggert JK.

Physiol Genomics. 2006 Oct 11;27(2):131-40. Epub 2006 Jul 18.

9.

A candidate gene for the mouse mutation tubby.

Noben-Trauth K, Naggert JK, North MA, Nishina PM.

Nature. 1996 Apr 11;380(6574):534-8.

PMID:
8606774
10.

Progression of cochlear and retinal degeneration in the tubby (rd5) mouse.

Ohlemiller KK, Hughes RM, Lett JM, Ogilvie JM, Speck JD, Wright JS, Faddis BT.

Audiol Neurootol. 1997 Jul-Aug;2(4):175-85.

PMID:
9390831
11.

Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina.

Ikeda S, He W, Ikeda A, Naggert JK, North MA, Nishina PM.

Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2706-12.

PMID:
10509669
12.

Delay of photoreceptor degeneration in tubby mouse by sulforaphane.

Kong L, Tanito M, Huang Z, Li F, Zhou X, Zaharia A, Yodoi J, McGinnis JF, Cao W.

J Neurochem. 2007 May;101(4):1041-52. Epub 2007 Mar 30.

13.

Retinal degeneration mutants in the mouse.

Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR.

Vision Res. 2002 Feb;42(4):517-25. Review.

14.

Sperm abnormalities in retinitis pigmentosa.

Connor WE, Weleber RG, DeFrancesco C, Lin DS, Wolf DP.

Invest Ophthalmol Vis Sci. 1997 Nov;38(12):2619-28.

PMID:
9375581
15.

Prominent neuronal-specific tub gene expression in cellular targets of tubby mice mutation.

Sahly I, Gogat K, Kobetz A, Marchant D, Menasche M, Castel M, Revah F, Dufier J, Guerre-Millo M, Abitbol MM.

Hum Mol Genet. 1998 Sep;7(9):1437-47.

PMID:
9700199
16.

Unravelling the genetics of deafness.

Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD.

Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Review.

PMID:
9153119
17.

Evidence of altered hypothalamic pro-opiomelanocortin/ neuropeptide Y mRNA expression in tubby mice.

Guan XM, Yu H, Van der Ploeg LH.

Brain Res Mol Brain Res. 1998 Aug 31;59(2):273-9.

PMID:
9729427
18.
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