Authors:
Mazeyrat, S
Saut, N
Grigoriev, V
Mahadevaiah, SK
Ojarikre, OA
Rattigan, A
Bishop, C
Eicher, EM
Mitchell, MJ
Burgoyne, PS
Citation: S. Mazeyrat et al., A Y-encoded subunit of the translation initiation factor Eif2 is essentialfor mouse spermatogenesis, NAT GENET, 29(1), 2001, pp. 49-53
Citation: Em. Eicher et Ll. Washburn, Does one gene determine whether a C57BL/6J-YPpos mouse will develop as a female or as an hermaphrodite?, J EXP ZOOL, 290(4), 2001, pp. 322-326
Citation: Ll. Washburn et al., C57BL/6J-T-associated sex reversal in mice is caused by reduced expressionof a Mus domesticus Sry allele, GENETICS, 158(4), 2001, pp. 1675-1681
Authors:
Bergstrom, DE
Young, M
Albrecht, KH
Eicher, EM
Citation: De. Bergstrom et al., Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination, GENESIS, 28(3-4), 2000, pp. 111-124
Authors:
Albrecht, KH
Capel, B
Washburn, LL
Eicher, EM
Citation: Kh. Albrecht et al., Defective mesonephric cell migration is associated with abnormal testis cord development in C57BL/6J XYMus (domesticus) mice, DEVELOP BIO, 225(1), 2000, pp. 26-36
Citation: B. Gwynn et al., Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism, BLOOD, 96(13), 2000, pp. 4227-4235
Authors:
Feng, LJ
Seymour, AB
Jiang, S
To, A
Peden, AA
Novak, EK
Zhen, LJ
Rusiniak, ME
Eicher, EM
Robinson, MS
Gorin, MB
Swank, RT
Citation: Lj. Feng et al., The beta 3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered inthe mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness, HUM MOL GEN, 8(2), 1999, pp. 323-330
Authors:
Jaubert, J
Jaubert, F
Martin, N
Washburn, LL
Lee, BK
Eicher, EM
Guenet, JL
Citation: J. Jaubert et al., Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3), P NAS US, 96(18), 1999, pp. 10278-10283