220 related articles for article (PubMed ID: 9094208)
1. Paternal transmission of the mouse Thp mutation is lethal in some genetic backgrounds.
Rogers I; Okano K; Varmuza S
Dev Genet; 1997; 20(1):23-8. PubMed ID: 9094208
[TBL] [Abstract][Full Text] [Related]
2. [Two doses of the paternal Tme gene do not compensate for the lethality of the Thp deletion in mice].
Agul'nik AI; Agul'nik SI; Rubinskiĭ AO
Genetika; 1990 Nov; 26(11):2076-8. PubMed ID: 2074014
[TBL] [Abstract][Full Text] [Related]
3. Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice.
Neumann PE; Frankel WN; Letts VA; Coffin JM; Copp AJ; Bernfield M
Nat Genet; 1994 Apr; 6(4):357-62. PubMed ID: 8054974
[TBL] [Abstract][Full Text] [Related]
4. Dominant lethality of the mouse skeletal mutation tail-short (Ts) is determined by the Ts allele from mating partners.
Ishijima J; Yasui H; Morishima M; Shiroishi T
Genomics; 1998 May; 49(3):341-50. PubMed ID: 9615218
[TBL] [Abstract][Full Text] [Related]
5. Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds.
Ludwig T; Eggenschwiler J; Fisher P; D'Ercole AJ; Davenport ML; Efstratiadis A
Dev Biol; 1996 Aug; 177(2):517-35. PubMed ID: 8806828
[TBL] [Abstract][Full Text] [Related]
6. Neural tube defects without neural crest defects in splotch mice.
Franz T
Teratology; 1992 Dec; 46(6):599-604. PubMed ID: 1290160
[TBL] [Abstract][Full Text] [Related]
7. Intraspecific mating with CzechII/Ei mice rescue lethality associated with loss of function mutations of the imprinted genes, Igf2r and Cdkn1c.
Hagan JP; Kozlov SV; Chiang Y; Sewell L; Stewart CL
Genomics; 2004 Nov; 84(5):836-43. PubMed ID: 15475262
[TBL] [Abstract][Full Text] [Related]
8. Identification of a new chemically induced allele (Lp(m1Jus)) at the loop-tail locus: morphology, histology, and genetic mapping.
Kibar Z; Underhill DA; Canonne-Hergaux F; Gauthier S; Justice MJ; Gros P
Genomics; 2001 Mar; 72(3):331-7. PubMed ID: 11401449
[TBL] [Abstract][Full Text] [Related]
9. Rescue of the T-associated maternal effect in mice carrying null mutations in Igf-2 and Igf2r, two reciprocally imprinted genes.
Filson AJ; Louvi A; Efstratiadis A; Robertson EJ
Development; 1993 Jul; 118(3):731-6. PubMed ID: 8076514
[TBL] [Abstract][Full Text] [Related]
10. Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene.
Wang ZQ; Fung MR; Barlow DP; Wagner EF
Nature; 1994 Dec; 372(6505):464-7. PubMed ID: 7984240
[TBL] [Abstract][Full Text] [Related]
11. Disruption of the mouse necdin gene results in early post-natal lethality.
Gérard M; Hernandez L; Wevrick R; Stewart CL
Nat Genet; 1999 Oct; 23(2):199-202. PubMed ID: 10508517
[TBL] [Abstract][Full Text] [Related]
12. Circletail, a new mouse mutant with severe neural tube defects: chromosomal localization and interaction with the loop-tail mutation.
Murdoch JN; Rachel RA; Shah S; Beermann F; Stanier P; Mason CA; Copp AJ
Genomics; 2001 Nov; 78(1-2):55-63. PubMed ID: 11707073
[TBL] [Abstract][Full Text] [Related]
13. Tail short variable: characterization of a new mouse mutant, and its possible analogy to certain human vascular disruption defects.
Seller MJ; Wallace ME
Teratology; 1993 Oct; 48(4):383-91. PubMed ID: 8278937
[TBL] [Abstract][Full Text] [Related]
14. Imprinting at the mouse Ins2 locus: evidence for cis- and trans-allelic interactions.
Duvillié B; Bucchini D; Tang T; Jami J; Pàldi A
Genomics; 1998 Jan; 47(1):52-7. PubMed ID: 9465295
[TBL] [Abstract][Full Text] [Related]
15. Two doses of the paternal Tme gene do not compensate the lethality of the Thp deletion.
Agulnik AI; Agulnik SI; Ruvinsky AO
J Hered; 1991; 82(4):351-3. PubMed ID: 1880396
[TBL] [Abstract][Full Text] [Related]
16. Imprinted expression of the Igf2r gene depends on an intronic CpG island.
Wutz A; Smrzka OW; Schweifer N; Schellander K; Wagner EF; Barlow DP
Nature; 1997 Oct; 389(6652):745-9. PubMed ID: 9338788
[TBL] [Abstract][Full Text] [Related]
17. Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia.
Ruvinsky I; Chertkov O; Borue XV; Agulnik SI; Gibson-Brown JJ; Lyle SR; Silver LM
Mamm Genome; 2002 Dec; 13(12):675-9. PubMed ID: 12514744
[TBL] [Abstract][Full Text] [Related]
18. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.
Kaneko-Ishino T; Kuroiwa Y; Miyoshi N; Kohda T; Suzuki R; Yokoyama M; Viville S; Barton SC; Ishino F; Surani MA
Nat Genet; 1995 Sep; 11(1):52-9. PubMed ID: 7550314
[TBL] [Abstract][Full Text] [Related]
19. Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.
Franke B; Klootwijk R; Hekking JW; de Boer RT; ten Donkelaar HJ; Mariman EC; van Straaten HW
Anat Embryol (Berl); 2003 Oct; 207(3):255-62. PubMed ID: 14523648
[TBL] [Abstract][Full Text] [Related]
20. Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.
Keller SA; Jones JM; Boyle A; Barrow LL; Killen PD; Green DG; Kapousta NV; Hitchcock PF; Swank RT; Meisler MH
Genomics; 1994 Sep; 23(2):309-20. PubMed ID: 7835879
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]