Eicher EM - Search Results

1

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. Feng L, et al. Among authors: eicher em. Hum Mol Genet. 1999 Feb;8(2):323-30. doi: 10.1093/hmg/8.2.323. Hum Mol Genet. 1999. PMID: 9931340

2

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. Zhang Q, et al. Among authors: eicher em. Nat Genet. 2003 Feb;33(2):145-53. doi: 10.1038/ng1087. Epub 2003 Jan 27. Nat Genet. 2003. PMID: 12548288

3

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. Gwynn B, et al. Among authors: eicher em. Blood. 2000 Dec 15;96(13):4227-35. Blood. 2000. PMID: 11110696 Free article.

4

Genetic organization of the agouti region of the mouse.

Siracusa LD, Russell LB, Eicher EM, Corrow DJ, Copeland NG, Jenkins NA. Siracusa LD, et al. Among authors: eicher em. Genetics. 1987 Sep;117(1):93-100. doi: 10.1093/genetics/117.1.93. Genetics. 1987. PMID: 3666442 Free PMC article.

5

Localization of the growth hormone gene to the distal half of mouse chromosome 11.

Elliott RW, Lee BK, Eicher EM. Elliott RW, et al. Among authors: eicher em. Genomics. 1990 Nov;8(3):591-4. doi: 10.1016/0888-7543(90)90051-u. Genomics. 1990. PMID: 2286379

6

The original pink-eyed dilution mutation (p) arose in Asiatic mice: implications for the H4 minor histocompatibility antigen, Myod1 regulation and the origin of inbred strains.

Brilliant MH, Ching A, Nakatsu Y, Eicher EM. Brilliant MH, et al. Among authors: eicher em. Genetics. 1994 Sep;138(1):203-11. doi: 10.1093/genetics/138.1.203. Genetics. 1994. PMID: 8001787 Free PMC article.

7

DNA sequence analysis of Sry alleles (subgenus Mus) implicates misregulation as the cause of C57BL/6J-Y(POS) sex reversal and defines the SRY functional unit.

Albrecht KH, Eicher EM. Albrecht KH, et al. Among authors: eicher em. Genetics. 1997 Nov;147(3):1267-77. doi: 10.1093/genetics/147.3.1267. Genetics. 1997. PMID: 9383069 Free PMC article.

8

Sry expression level and protein isoform differences play a role in abnormal testis development in C57BL/6J mice carrying certain Sry alleles.

Albrecht KH, Young M, Washburn LL, Eicher EM. Albrecht KH, et al. Among authors: eicher em. Genetics. 2003 May;164(1):277-88. doi: 10.1093/genetics/164.1.277. Genetics. 2003. PMID: 12750339 Free PMC article.

9

Normal testis determination in the mouse depends on genetic interaction of a locus on chromosome 17 and the Y chromosome.

Washburn LL, Eicher EM. Washburn LL, et al. Among authors: eicher em. Genetics. 1989 Sep;123(1):173-9. doi: 10.1093/genetics/123.1.173. Genetics. 1989. PMID: 2806881 Free PMC article.

10

Meiotic abnormalities in hybrid mice of the C57BL/6J x Mus spretus cross suggest a cytogenetic basis for Haldane's rule of hybrid sterility.

Hale DW, Washburn LL, Eicher EM. Hale DW, et al. Among authors: eicher em. Cytogenet Cell Genet. 1993;63(4):221-34. doi: 10.1159/000133539. Cytogenet Cell Genet. 1993. PMID: 8500353

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