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Items: 1 to 50 of 146

1.

Sex reversal in C57BL/6J XY mice caused by increased expression of ovarian genes and insufficient activation of the testis determining pathway.

Correa SM, Washburn LL, Kahlon RS, Musson MC, Bouma GJ, Eicher EM, Albrecht KH.

PLoS Genet. 2012;8(4):e1002569. doi: 10.1371/journal.pgen.1002569. Epub 2012 Apr 5.

2.

New candidate genes identified for controlling mouse gonadal sex determination and the early stages of granulosa and Sertoli cell differentiation.

Bouma GJ, Hudson QJ, Washburn LL, Eicher EM.

Biol Reprod. 2010 Feb;82(2):380-9. doi: 10.1095/biolreprod.109.079822. Epub 2009 Oct 28.

3.

Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice.

Wilhelm D, Washburn LL, Truong V, Fellous M, Eicher EM, Koopman P.

Mech Dev. 2009 May-Jun;126(5-6):324-36. doi: 10.1016/j.mod.2009.02.006. Epub 2009 Mar 6.

4.

The mouse A/HeJ Y chromosome: another good Y gone bad.

Hunt PA, Jackson JM, Horan S, Lawson CA, Grindell L, Washburn LL, Eicher EM.

Chromosome Res. 2008;16(4):623-36. doi: 10.1007/s10577-008-1216-8. Epub 2008 May 20.

PMID:
18483871
5.

The chromosome 11 region from strain 129 provides protection from sex reversal in XYPOS mice.

Nikolova G, Sinsheimer JS, Eicher EM, Vilain E.

Genetics. 2008 May;179(1):419-27. doi: 10.1534/genetics.108.088088. Epub 2008 May 5.

6.

Correct dosage of Fog2 and Gata4 transcription factors is critical for fetal testis development in mice.

Bouma GJ, Washburn LL, Albrecht KH, Eicher EM.

Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):14994-9. Epub 2007 Sep 11.

7.

Transcriptional profile of mouse pre-granulosa and Sertoli cells isolated from early-differentiated fetal gonads.

Bouma GJ, Affourtit JP, Bult CJ, Eicher EM.

Gene Expr Patterns. 2007 Jan;7(1-2):113-23. Epub 2006 Jun 6.

PMID:
16839824
8.

Gonadal sex reversal in mutant Dax1 XY mice: a failure to upregulate Sox9 in pre-Sertoli cells.

Bouma GJ, Albrecht KH, Washburn LL, Recknagel AK, Churchill GA, Eicher EM.

Development. 2005 Jul;132(13):3045-54.

9.

Using real time RT-PCR analysis to determine multiple gene expression patterns during XX and XY mouse fetal gonad development.

Bouma GJ, Hart GT, Washburn LL, Recknagel AK, Eicher EM.

Gene Expr Patterns. 2004 Nov;5(1):141-9.

PMID:
15533830
10.

New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.

Lorenz-Depiereux B, Guido VE, Johnson KR, Zheng QY, Gagnon LH, Bauschatz JD, Davisson MT, Washburn LL, Donahue LR, Strom TM, Eicher EM.

Mamm Genome. 2004 Mar;15(3):151-61.

11.

Overlapping deletions spanning the proximal two-thirds of the mouse t complex.

Bergstrom DE, Bergstrom RA, Munroe RJ, Lee BK, Browning VL, You Y, Eicher EM, Schimenti JC.

Mamm Genome. 2003 Dec;14(12):817-29.

12.

High-resolution genetic map of X-linked juvenile-type granulosa cell tumor susceptibility genes in mouse.

Dorward AM, Shultz KL, Ackert-Bicknell CL, Eicher EM, Beamer WG.

Cancer Res. 2003 Dec 1;63(23):8197-202.

13.
14.

Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6.

Zhang Q, Zhao B, Li W, Oiso N, Novak EK, Rusiniak ME, Gautam R, Chintala S, O'Brien EP, Zhang Y, Roe BA, Elliott RW, Eicher EM, Liang P, Kratz C, Legius E, Spritz RA, O'Sullivan TN, Copeland NG, Jenkins NA, Swank RT.

Nat Genet. 2003 Feb;33(2):145-53. Epub 2003 Jan 27.

PMID:
12548288
15.

Gonadal differentiation, sex determination and normal Sry expression in mice require direct interaction between transcription partners GATA4 and FOG2.

Tevosian SG, Albrecht KH, Crispino JD, Fujiwara Y, Eicher EM, Orkin SH.

Development. 2002 Oct;129(19):4627-34.

16.
17.
18.

A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis.

Mazeyrat S, Saut N, Grigoriev V, Mahadevaiah SK, Ojarikre OA, Rattigan A, Bishop C, Eicher EM, Mitchell MJ, Burgoyne PS.

Nat Genet. 2001 Sep;29(1):49-53.

PMID:
11528390
19.
20.

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.

Gwynn B, Ciciotte SL, Hunter SJ, Washburn LL, Smith RS, Andersen SG, Swank RT, Dell'Angelica EC, Bonifacino JS, Eicher EM, Peters LL.

Blood. 2000 Dec 15;96(13):4227-35.

PMID:
11110696
21.

Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination.

Bergstrom DE, Young M, Albrecht KH, Eicher EM.

Genesis. 2000 Nov-Dec;28(3-4):111-24.

22.
23.

Sry induces cell proliferation in the mouse gonad.

Schmahl J, Eicher EM, Washburn LL, Capel B.

Development. 2000 Jan;127(1):65-73.

24.

Migration of mesonephric cells into the mammalian gonad depends on Sry.

Capel B, Albrecht KH, Washburn LL, Eicher EM.

Mech Dev. 1999 Jun;84(1-2):127-31.

25.

Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3).

Jaubert J, Jaubert F, Martin N, Washburn LL, Lee BK, Eicher EM, Guénet JL.

Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10278-83.

26.

Genetic and physical mapping of the dreher locus on mouse chromosome 1.

Bergstrom DE, Gagnon LH, Eicher EM.

Genomics. 1999 Aug 1;59(3):291-9.

PMID:
10444330
27.

The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.

Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT.

Hum Mol Genet. 1999 Feb;8(2):323-30.

PMID:
9931340
28.

Multigenic and imprinting control of ovarian granulosa cell tumorigenesis in mice.

Beamer WG, Shultz KL, Tennent BJ, Nadeau JH, Churchill GA, Eicher EM.

Cancer Res. 1998 Aug 15;58(16):3694-9.

30.

Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal.

Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC.

Nat Genet. 1996 Oct;14(2):206-9.

PMID:
8841197
31.
32.

Sex reversal in C57BL/6J-YPOS mice corrected by a Sry transgene.

Eicher EM, Shown EP, Washburn LL.

Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1333):263-8; discussion 268-9.

PMID:
8570690
33.

Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genes.

Servadio A, McCall A, Zoghbi H, Eicher EM.

Genomics. 1995 Oct 10;29(3):812-3. No abstract available.

PMID:
8575786
34.
35.

The gene encoding the erythrocyte membrane skeleton protein dematin (Epb4.9) maps to mouse chromosome 14.

Peters LL, Eicher EM, Azim AC, Chishti AH.

Genomics. 1995 Apr 10;26(3):634-5. No abstract available.

PMID:
7607697
36.

Deletion mapping by immunoselection against the H-Y histocompatibility antigen further resolves the Sxra region of the mouse Y chromosome and reveals complexity of the Hya locus.

King TR, Christianson GJ, Mitchell MJ, Bishop CE, Scott D, Ehrmann I, Simpson E, Eicher EM, Roopenian DC.

Genomics. 1994 Nov 1;24(1):159-68.

PMID:
7896271
38.

The ubiquitous subunit of the globin enhancer-binding protein NF-E2 (Nfe2u) maps to mouse chromosome 5.

Peters LL, Eicher EM.

Genomics. 1994 Jul 15;22(2):490-1. No abstract available.

PMID:
7806243
39.

Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects.

Davisson MT, Cook SA, Johnson KR, Eicher EM.

J Hered. 1994 Mar-Apr;85(2):134-6. No abstract available.

PMID:
8182278
40.

Sex and trinucleotide repeats.

Eicher EM.

Nat Genet. 1994 Mar;6(3):221-3. No abstract available.

PMID:
8012379
41.

The exon-intron structure and chromosomal localization of the mouse macrophage mannose receptor gene Mrc1: identification of a Ricin-like domain at the N-terminus of the receptor.

Harris N, Peters LL, Eicher EM, Rits M, Raspberry D, Eichbaum QG, Super M, Ezekowitz RA.

Biochem Biophys Res Commun. 1994 Jan 28;198(2):682-92.

PMID:
8297379
42.

Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2.

Peters LL, Andrews NC, Eicher EM, Davidson MB, Orkin SH, Lux SE.

Nature. 1993 Apr 22;362(6422):768-70. Erratum in: Nature 1994 Sep 22;371(6495):358.

PMID:
8469289
43.
44.

Molecular markers that define the distal ends of mouse autosomes 4, 13, and 19 and the sex chromosomes.

Eicher EM, Shown EP.

Mamm Genome. 1993;4(4):226-9. No abstract available.

PMID:
8499658
45.

Corrected centromere orientation for mouse chromosome 19 MIT markers.

Eicher EM, Shown EP, Bhat D, Seldin MF.

Mamm Genome. 1993;4(4):223-5. No abstract available.

PMID:
8499657
46.

Chromosomal location and isoform analysis of mouse Fc epsilon RII/CD23.

Conrad DH, Kozak CA, Vernachio J, Squire CM, Rao M, Eicher EM.

Mol Immunol. 1993 Jan;30(1):27-33. Erratum in: Mol Immunol 1993 Feb;30(3):331.

PMID:
8417372
47.

Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci.

Watson ML, Rao JK, Gilkeson GS, Ruiz P, Eicher EM, Pisetsky DS, Matsuzawa A, Rochelle JM, Seldin MF.

J Exp Med. 1992 Dec 1;176(6):1645-56.

48.

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.

49.

ABRUPT CLINE FOR SEX CHROMOSOMES IN A HYBRID ZONE BETWEEN TWO SPECIES OF MICE.

Tucker PK, Sage RD, Warner J, Wilson AC, Eicher EM.

Evolution. 1992 Aug;46(4):1146-1163. doi: 10.1111/j.1558-5646.1992.tb00625.x.

50.

Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.

Lyon MF, King TR, Gondo Y, Gardner JM, Nakatsu Y, Eicher EM, Brilliant MH.

Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):6968-72.

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