Biology Reference
In-Depth Information
Yamagata H., Miki T., Nakagawa M., Johnson K., Deka R., Ogihara T.
(1996) Association of CTG
repeats and the 1-kb
Alu
insertion/deletion polymorphism at the myotonin protein kinase gene in
the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation.
Hum. Genet.
97
: 145-147.
Yanagisawa J., Fujii K., Nagafuchi S.
et al.
(1996) A unique origin and multistep process for the
generation of expanded DRPLA triplet repeats.
Hum. Molec. Genet.
5
: 373-379.
Yokoi T., Kosaka Y., Chida M., Chiba K., Nakamura H., Ishizaki T., Kinoshita M., Sato K.,
Gonzalez F.J., Kamataki T.
(1996) A new
CYP2D6
allele with a nine base insertion in exon 9 in a
Japanese population associated with poor metabolizer phenotype.
Pharmacogenetics
6
: 395-401.
Yoneda K., Hohl D., McBride O.W., Wang M., Cehrs K.U., Idler W.W., Steinert P.M.
(1992) The
human loricrin gene.
J. Biol. Chem
.
267
: 18 060-18 066.
Yulug I.G., Yulug A., Fisher E.M.C.
(1995) The frequency and position of
Alu
repeats in cDNAs, as
determined by database searching.
Genomics
27
: 544-548.
Zhu Z.B., Hsieh S.L., Bentley R., Campbell R.D., Volanakis J.E.
(1992) A variable number of
tandem repeats locus within the human complement C2 gene is associated with a retroposon
derived from a human endogenous retrovirus.
J. Exp. Med.
175
: 1783-1787.
Zhu Z.B., Jian B., Volanakis J.E.
(1994) Ancestry of SINE-R.C2, a human-specific retroposon.
Hum.
Genet
.
93
: 545-551.
Zietkiewicz E., Richer C., Sinnett D., Labuda D.
(1998) Monophyletic origin of
Alu
elements in
primates.
J. Mol. Evol
.
47
: 172-182.
Zucman-Rossi J., Batzer M.A., Stoneking M., Delattre O., Thomas G.
(1997) Interethnic
polymorphism of EWS intron 6: genome plasticity mediated by
Alu
retroposition and
recombination.
Hum. Genet
.
99
: 357-363.