Biology Reference
In-Depth Information
Rorman E., Scheinker V., Grabowski G.A.
(1992) Structure and evolution of the human prosaposin
chromosomal gene.
Genomics
13
: 312-318.
Rouquier S., Taviaux S., Trask B.J., Brand-Arpon V., van den Engh G., Demaille J., Giogi D.
(1998) Distribution of olfactory receptor genes in the human genome.
Nature Genet
.
18
: 243-250.
Russek S.J., Farb D.H.
(1994) Mapping of the
β
2
subunit gene (
GABRB2
) to microdissected human
chromosome 5q34-q35 defines a gene cluster for the most abundant GABA
A
receptor isoform.
Genomics
23
: 528-533.
Sastry K., Herman G.A., Day L., Deignan E., Bruns G., Morton C.C., Ezekowitz R.A.B.
(1989)
The human mannose-binding protein gene.
J. Exp. Med
.
170
: 1175-1189.
Schimenti J.C., Duncan C.H.
(1984) Ruminant globin gene structures suggest an evolutionary role
for
Alu
-type repeats.
Nucleic Acids Res
.
12
: 1641-1655.
Schwartz A., Chan D.C., Brown L.G., Alagappan R., Pettay D., Disteche C., McGillivray B., de la
Chapelle A., Page D.C.
(1998) Reconstructing hominid evolution: X-homologous block, created
by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination.
Hum.
Molec. Genet
.
7
: 1-11.
Seeman G.H., Rein R.S., Brown C.S., Ploegh H.L.
(1986) Gene conversion-like mechanisms may
generate polymorphism in human class I genes.
EMBO J
.
5
: 547-552.
Seperack P., Slatkin M., Arnheim N.
(1988) Linkage equilibrium in human ribosomal genes:
implications for multigene family evolution.
Genetics
119
: 943-949.
Sharp P.M., Li W.-H.
(1987) Ubiquitin genes as a paradigm of concerted evolution of tandem
repeats.
J. Mol. Evol
.
25
: 58-64.
Shaw J.-P., Marks J., Shen C.-K.J.
(1991) The adult
-globin locus of Old World monkeys: an
abrupt breakdown of sequence similarity to human is defined by an
Alu
family repeat insertion
site.
J. Mol. Evol
.
33
: 506-513.
Shen S., Slightom J.L., Smithies O.
(1981) A history of the human fetal globin gene duplication.
Cell
26
: 191-203.
Shiroishi T., Sagai T., Moriwaki K.
(1993) Hotspots of meiotic recombination in the mouse major
histocompatibility complex.
Genetica
88
: 187-196.
Shyue S.K., Li L., Chang B.H., Li W.H.
(1994) Intronic gene conversion in the evolution of human
X-linked color vision genes.
Mol. Biol. Evol
.
11
: 548-551.
Shyue S.K., Hewett-Emmett D., Sperling H.G., Hunt D.M., Bowmaker J.K., Mollon J.D.,
Li W.H.
(1995) Adaptive evolution of color vision genes in higher primates.
Science
269
:
1265-1267.
Small K., Iber J., Warren S.T.
(1997) Emerin deletion reveals a common X-chromosome inversion
mediated by inverted repeats.
Nature Genet
.
16
: 96-99.
Smith G.R.
(1983) Chi hotspots of generalized recombination.
Cell
34
: 709-710.
Soret J., Gattoni R., Guyon C., Sureau A., Popielarz M., Le Rouzic E., Dumon S., Apiou F.,
Dutrillaux B., Voss H., Ansorge W., Stevenin J., Perbal B.
(1998) Characterization of SRp46, a
novel human SR splicing factor encoded by a PR264/SC35 retropseudogene.
Mol. Cell. Biol
.
18
:
4924-4934.
Spurdle A., Jenkins T.
(1992) The inverted Y-chromosome polymorphism in the Gujarati muslim
Indian population of South Africa has a single origin.
Hum. Hered
.
42
: 330-332.
Stoeckert C.J., Collins F.S., Weissman S.
(1984) Human fetal globin DNA sequences suggest novel
conversion event.
Nucleic Acids Res
.
12
: 4469-4479.
Tagle D.A., Slightom J.L., Jones R.T., Goodman M.
(1991) Concerted evolution led to high
expression of a prosimian primate
globin gene locus.
J. Biol. Chem
.
266
: 7469-7480.
Takagi Y., Omura T., Go M.
(1991) Evolutionary origin of thyroglobulin by duplication of esterase
gene.
FEBS Letts
282
: 17-22.
Tasaki Y., Fukuda S., Lio M., Miwa R., Imai T., Sugano S., Yoshie O., Hughes A.L., Nomiyama
H.
(1999) Chemokine PARC gene (
SCYA18
) generated by fusion of two MIP-1 alpha/LD78 alpha-
like genes.
Genomics
55
: 353-357.
Thompson C.B.
(1995) New insights into V(D)J recombination and its role in the evolution of the
immune system.
Immunity
3
: 531-539.
Toder R., Rappold G.A., Schiebel K., Schempp W.
(1995)
ANT3
and
STS
are autosomal in
prosimian lemurs: implications for the evolution of the pseudoautosomal region.
Hum. Genet
.
95
:
22-28.
