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Results 11-18 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
1999
Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)
Lee, M.H.
;
Shroff, R.
;
Cooper, S.
;
Hope, R.
1998
Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
Whitmore, S.
;
Settasatian, C.
;
Crawford, J.
;
Lower, K.
;
McCallum, B.
;
Seshadri, R.
;
Cornelisse, C.
;
Moerland, E.
;
Cleton-Jansen, A.M.
;
Tipping, A.
;
Mathew, C.
;
Savnio, M.
;
Savoia, A.
;
Verlander, P.
;
Auerbach, A.
;
Van Berkel, C.
;
Pronk, J.
;
Doggett, N.
;
Callen, D.
1998
ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, & is shown to be expressed in primitive hematopoietic precursors.
Kuss, B.
;
O'Neill, G.
;
Eyre, H.
;
Doggett, N.
;
Callen, D.
;
Davey, R.
1997
Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3
Sood, R.
;
Blake, T.
;
Aksentijevich, I.
;
Wood, G.
;
Chen, X.
;
Gardner, D.
;
Shelton, D.
;
Mangelsdorf, M.
;
Orsborn, A.
;
Pras, E.
;
Balow, J.
;
Centola, M.
;
Deng, Z.
;
Zaks, N.
;
Chen, X.
;
Richards, N.
;
Fischel-Ghodsian, N.
;
Rotter, J.
;
Pras, M.
;
Shohat, M.
;
et al.
1997
The genome organisation of the Fanconi Anemia Group A (FAA) Gene
Ianzano, L.
;
d'Apolito, M.
;
Centra, M.
;
Savino, M.
;
Levran, O.
;
Auerbach, A.
;
Cleton-Jansen, A.M.
;
Doggett, N.
;
Pronk, J.
;
Tipping, A.
;
Gibson, R.
;
Mathew, C.
;
Whitmore, S.
;
Apostolou, S.
;
Callen, D.
;
Zelante, L.
;
Savoia, A.
1997
Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators
Gecz, J.
;
Bielby, S.
;
Sutherland, G.
;
Mulley, J.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
Discover
Author
5
Callen, D.
4
Doggett, N.
3
Aksentijevich, I.
3
Blake, T.
3
Centola, M.
3
Chen, X.
3
Deng, Z.
3
et al.
3
Saint, R.
3
Sood, R.
.
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Subject
17
Molecular Sequence Data
12
Base Sequence
12
Humans
10
Amino Acid Sequence
8
Animals
8
Sequence Homology, Amino Acid
7
Sequence Analysis, DNA
6
DNA, Complementary
5
Chromosomes, Human, Pair 16
5
Exons
.
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Date issued
2
1999
6
1998
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1997
4
1996