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.
3. Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7. Jones JM; Meisler MH; Seldin MF; Lee BK; Eicher EM Genomics; 1992 Sep; 14(1):197-9. PubMed ID: 1358794 [TBL] [Abstract][Full Text] [Related]
4. High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6. Weber JS; Jang W; Simin K; Lu W; Yu J; Meisler MH Genomics; 1998 Nov; 54(1):107-15. PubMed ID: 9806835 [TBL] [Abstract][Full Text] [Related]
5. A candidate gene for the mouse mutation tubby. Noben-Trauth K; Naggert JK; North MA; Nishina PM Nature; 1996 Apr; 380(6574):534-8. PubMed ID: 8606774 [TBL] [Abstract][Full Text] [Related]
6. Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8. Janaswami PM; Birkenmeier EH; Cook SA; Rowe LB; Bronson RT; Davisson MT Genomics; 1997 Feb; 40(1):101-7. PubMed ID: 9070925 [TBL] [Abstract][Full Text] [Related]
7. Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss. Ikeda A; Zheng QY; Rosenstiel P; Maddatu T; Zuberi AR; Roopenian DC; North MA; Naggert JK; Johnson KR; Nishina PM Hum Mol Genet; 1999 Sep; 8(9):1761-7. PubMed ID: 10441341 [TBL] [Abstract][Full Text] [Related]
8. Abnormal cholinergic and GABAergic vascular innervation in the hypothalamic arcuate nucleus of obese tub/tub mice. Bäckberg M; Meister B Synapse; 2004 Jun; 52(4):245-57. PubMed ID: 15103691 [TBL] [Abstract][Full Text] [Related]
9. Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7. Chae TH; Allen KM; Davisson MT; Sweet HO; Walsh CA Mamm Genome; 2002 May; 13(5):239-44. PubMed ID: 12016511 [TBL] [Abstract][Full Text] [Related]
11. Fine genetic mapping of the Hyp mutation on mouse chromosome X. Du L; Desbarats M; Cornibert S; Malo D; Ecarot B Genomics; 1996 Mar; 32(2):177-83. PubMed ID: 8833143 [TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans. Nishina PM; North MA; Ikeda A; Yan Y; Naggert JK Genomics; 1998 Dec; 54(2):215-20. PubMed ID: 9828123 [TBL] [Abstract][Full Text] [Related]
13. 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; 27(2):131-40. PubMed ID: 16849632 [TBL] [Abstract][Full Text] [Related]
14. Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations. Street VA; Robinson LC; Erford SK; Tempel BL Genomics; 1995 Sep; 29(1):123-30. PubMed ID: 8530061 [TBL] [Abstract][Full Text] [Related]
15. Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome. Candille SI; Pardue MT; McCall MA; Peachey NS; Gregg RG Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2748-51. PubMed ID: 10509675 [TBL] [Abstract][Full Text] [Related]
16. The mouse mutation sarcosinemia (sar) maps to chromosome 2 in a region homologous to human 9q33-q34. Brunialti AL; Harding CO; Wolff JA; Guénet JL Genomics; 1996 Aug; 36(1):182-4. PubMed ID: 8812433 [TBL] [Abstract][Full Text] [Related]
17. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level. Mohlke KL; Purkayastha AA; Westrick RJ; Ginsburg D Genomics; 1998 Nov; 54(1):19-30. PubMed ID: 9806826 [TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 10629044 [TBL] [Abstract][Full Text] [Related]
19. Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. Sidjanin DJ; Grimes PA; Pretsch W; Neuhäuser-Klaus A; Favor J; Stambolian DE Invest Ophthalmol Vis Sci; 1997 Nov; 38(12):2502-7. PubMed ID: 9375568 [TBL] [Abstract][Full Text] [Related]