Biology Reference
In-Depth Information
Thiel C., Bontrop R.E., Lanchbury J.S.
(1995) Structure and diversity of the T-cell receptor α
chain
in rhesus macaque and chimpanzee.
Hum. Immunol
.
43
: 85-94.
Thomas G.H., Newbern E.C., Korte C.C., Bales M.A., Muse S.V., Clark A.G., Kiehart D.P.
(1997)
Intragenic duplication and divergence in the spectrin superfamily of proteins.
Mol. Biol. Evol
.
14
:
1285-1295.
Timchenko L.T., Caskey C.T.
(1996) Trinucleotide repeat disorders in humans: discussions of
mechanisms and medical issues.
FASEB J
.
10
: 1589-1597.
Timms K.M., Lu F., Shen Y., Pierson C.A., Muzny D.M., Gu Y., Nelson D.L., Gibbs R.A.
(1995)
130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human
iduronate-2-sulfate sulfatase locus.
Genome Res
.
5
: 71-78.
Ting C.N., Rosenberg M.P., Snow C.M., Samuelson L.C., Meisler M.H.
(1992) Endogenous
retroviral sequences are required for tissue-specific expression of a human salivary amylase gene.
Genes Devel
.
6
: 1457-1465.
Tishkoff S.A., Ruano G., Kidd J.R., Kidd K.K.
(1996) Distribution and frequency of a polymorphic
Alu
insertion at the plasminogen activator locus in humans.
Hum. Genet
.
97
: 759-764.
Tishkoff S.A., Goldman A., Calafell F., Speed W.C., Deinard A.S., Bonné-Tamir B., Kidd J.R.,
Pakstis A.J., Jenkins T., Kidd K.K.
(1998) A global haplotype analysis of the myotonic dystrophy
locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy
mutations.
Am. J. Hum. Genet
.
62
: 1389-1402.
Toribara N.W., Gum J.R., Culhane P.J., Lagace R.E., Hicks J.W., Petersen G.M., Kim Y.S.
(1991)
MUC-2 human small intestinal mucin gene structure: repeated arrays and polymorphism.
J. Clin.
Invest
.
88
: 1005-1013.
Toyosawa S., O'hUigin C., Figueroa F., Tichy H., Klein J.
(1998) Identification and
characterization of amelogenin genes in monotremes, reptiles, and amphibians.
Proc. Natl. Acad.
Sci. USA
95
: 13 056-13 061.
Trachtulec Z., Hamvas R.M.J., Forejt J., Lehrach H.R., Vincek V., Klein J.
(1997) Linkage of
TATA-binding protein and proteasome subunit C5 genes in mice and humans reveals synteny
conserved between mammals and invertebrates.
Genomics
44
: 1-7.
Trask B.J., Friedman C., Martin-Gallardo A.
et al
.
(1998a) Members of the olfactory receptor gene
family are contained in large blocks of DNA duplicated polymorphically near the ends of human
chromosomes.
Hum. Molec. Genet.
7
: 13-26.
Trask B.J., Massa M., Brand-Arpon V., Chan K., Friedman C., Nguyen O.T.H., Eichler E., van
den Engh G., Rouquier S., Shizuya H., Giorgi D.
(1998b) Large multi-chromosomal duplications
encompass many members of the olfactory receptor gene family in the human genome.
Hum.
Molec. Genet.
7
: 2007-2020.
Trifonov E.N., Bettecken T.
(1997) Sequence fossils, triplet expansion, and reconstruction of earliest
codons.
Gene
205
: 1-6.
Tseng H.
(1997) Complementary oligonucleotides and the origin of the mammalian involucrin gene.
Gene
194
: 87-95.
Tu A.Y., Deeb S.S., Iwasaki L., Day J.R., Albers J.J.
(1995) Organization of human phospholipid
transfer protein gene.
Biochem. Biophys. Res. Commun.
207
: 552-558.
Ulvsbäck M., Lundwall A.
(1997) Cloning of the semenogelin II gene of the rhesus monkey.
Duplications of 360 bp extend the coding region in man, rhesus monkey and baboon.
Eur. J.
Biochem
.
245
: 25-31.
Urquhart A., Gill P.
(1993) Tandem-repeat internal mapping (TRIM) of the involucrin gene: repeat
number and repeat-pattern polymorphism within a coding region in human populations.
Am. J.
Hum. Genet
.
53
: 279-286.
Valdes A.M., Slatkin N., Freimer N.B.
(1993) Allele frequencies at microsatellite loci: the stepwise
mutation model revisited.
Genetics
133
: 737-749.
van der Hoek Y.Y., Wittekoek M.E., Beisiegel U., Kastelein J.J., Koschinsky M.L.
(1993) The
apolipoprotein(a) kringle IV repeats which differ from the major repeat kringle are present in
variably sized isoforms.
Hum. Molec. Genet
.
2
: 361-366.
Vanin E.
(1984) Processed pseudogenes: characteristics and evolution.
Biochim. Biophys. Acta
782
:
231-246.
Verkerk A.J.M.H., Pieretti M., Sutcliffe J.S.
et al.
(1991) Identification of a gene (
FMR1
)
containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation
in fragile X syndrome.
Cell
65
: 905-914.
