Below are the most recent publications written about "Chromosomes, Mammalian" by people in Profiles.
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Wang M, Sips P, Khin E, Rotival M, Sun X, Ahmed R, Widjaja AA, Schafer S, Yusoff P, Choksi PK, Ko NS, Singh MK, Epstein D, Guan Y, Hou?tek J, Mracek T, Nuskova H, Mikell B, Tan J, Pesce F, Kolar F, Bottolo L, Mancini M, Hubner N, Pravenec M, Petretto E, MacRae C, Cook SA. Wars2 is a determinant of angiogenesis. Nat Commun. 2016 07 08; 7:12061.
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Schipler A, Mladenova V, Soni A, Nikolov V, Saha J, Mladenov E, Iliakis G. Chromosome thripsis by DNA double strand break clusters causes enhanced cell lethality, chromosomal translocations and 53BP1-recruitment. Nucleic Acids Res. 2016 09 19; 44(16):7673-90.
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Lo CL, Shen F, Baumgarner K, Cramer MJ, Lossie AC. Identification of 129S6/SvEvTac-specific polymorphisms on mouse chromosome 11. DNA Cell Biol. 2012 Mar; 31(3):402-14.
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Yokohama A, Mishra A, Mitsui T, Becknell B, Johns J, Curphey D, Blaser BW, Vandeusen JB, Mao H, Yu J, Caligiuri MA. A novel mouse model for the aggressive variant of NK cell and T cell large granular lymphocyte leukemia. Leuk Res. 2010 Feb; 34(2):203-9.
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Astrof S, Kirby A, Lindblad-Toh K, Daly M, Hynes RO. Heart development in fibronectin-null mice is governed by a genetic modifier on chromosome four. Mech Dev. 2007 Aug; 124(7-8):551-8.
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Jones HC, Chen GF, Yehia BR, Carter BJ, Akins EJ, Wolpin LC. Single and multiple congenic strains for hydrocephalus in the H-Tx rat. Mamm Genome. 2005 Apr; 16(4):251-61.
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Koratkar R, Silverman KA, Pequignot E, Hauck WW, Buchberg AM, Siracusa LD. Analysis of reciprocal congenic lines reveals the C3H/HeJ genome to be highly resistant to ApcMin intestinal tumorigenesis. Genomics. 2004 Nov; 84(5):844-52.
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Ferraro TN, Golden GT, Smith GG, Martin JF, Lohoff FW, Gieringer TA, Zamboni D, Schwebel CL, Press DM, Kratzer SO, Zhao H, Berrettini WH, Buono RJ. Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene. Mamm Genome. 2004 Apr; 15(4):239-51.