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Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome.
Published in:
Nature, 1983, v. 302, n. 5906, p. 346, doi. 10.1038/302346a0
By:
- Goodfellow, P.;
- Banting, G.;
- Sheer, D.;
- Ropers, H. H.;
- Caine, A.;
- Ferguson-Smith, M. A.;
- Povey, S.;
- Voss, R.
Publication type:
Article
cDNA and Genomic Clones Encoding the Human Muscle Acetylcholine Receptor.
Published in:
Annals of the New York Academy of Sciences, 1993, v. 681, n. 1, p. 165, doi. 10.1111/j.1749-6632.1993.tb22882.x
By:
- BEESON, D.;
- VINCENT, A.;
- MORRIS, A.;
- BRYDSON, M.;
- JACOBSON, L.;
- BAGGI, F.;
- JEREMIAH, S.;
- POVEY, S.;
- NEWSOM-DAVIS, J.
Publication type:
Article
Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataseta.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 256, doi. 10.1111/j.1749-6632.1991.tb37767.x
By:
- HAINES, J. L.;
- AMOS, J.;
- ATTWOOD, J.;
- BECH-HANSEN, N. T.;
- BURLEY, M.;
- CONNEALLY, P. M.;
- CONNOR, J. M.;
- FAHSOLD, R.;
- FLODMAN, P.;
- FRYER, A.;
- HALLEY, D. J. J.;
- JEWELL, A.;
- JANSSEN, L. A. J.;
- KANDT, R.;
- NORTHRUP, H.;
- OSBORNE, J.;
- PERICAK-VANCE, M.;
- POVEY, S.;
- SAMPSON, J.;
- SHORT, M. P.
Publication type:
Article
An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methodsa.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 298, doi. 10.1111/j.1749-6632.1991.tb37771.x
By:
- POVEY, S.;
- ATTWOOD, J.;
- JANSSEN, L. A. J.;
- BURLEY, M.;
- SMITH, M.;
- FLODMAN, P.;
- MORTON, N. E.;
- EDWARDS, J. H.;
- SAMPSON, J. R.;
- YATES, J. R. W.;
- HAINES, J. L.;
- AMOS, J.;
- SHORT, M. P.;
- SANDKUYL, L. A.;
- HALLEY, D. J. J.;
- FRYER, A. E.;
- BECH-HANSEN, T.;
- MUELLER, R.;
- AL-GHAZALI, L.;
- SUPER, M.
Publication type:
Article
A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23a.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 306, doi. 10.1111/j.1749-6632.1991.tb37772.x
By:
- JANSSEN, L. A. J.;
- POVEY, S.;
- ATTWOOD, J.;
- SANDKUYL, L. A.;
- LINDHOUT, D.;
- FLODMAN, P.;
- SMITH, M.;
- SAMPSON, J. R.;
- HAINES, J. L.;
- MERKENS, E. C.;
- FLEURY, P.;
- SHORT, P.;
- AMOS, J.;
- HALLEY, D. J. J.
Publication type:
Article
Characterisation of human cell lines and differentiation from HeLa by enzyme typing.
Published in:
Nature, 1976, v. 264, n. 5581, p. 60, doi. 10.1038/264060b0
By:
- POVEY, S.;
- HOPKINSON, D. A.;
- HARRIS, HARRY;
- FRANKS, L. M.
Publication type:
Article
Fusion of rous-sarcoma-virus-transformed rat cells to morphologically normal human or rat cells results in transcriptional suppression of the provirus that depends on its chromosomal integration site.
Published in:
International Journal of Cancer, 1990, v. 46, n. 2, p. 220, doi. 10.1002/ijc.2910460213
By:
- Green, A. R.;
- Poole, C. J.;
- Povey, S. M.;
- Rowe, D.;
- Searle, S.;
- Wyke, J. A.
Publication type:
Article
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: A study of 17 cases.
Published in:
Prenatal Diagnosis, 1992, v. 12, n. 4, p. 235, doi. 10.1002/pd.1970120402
By:
- Abbott, C. M.;
- Lovegrove, J. U.;
- Whitehouse, D. B.;
- Hopkinson, D. A.;
- Povey, S.
Publication type:
Article
Reduction of graft-versus-host disease in neonatal F1 hybrid mice.
Published in:
Clinical & Experimental Immunology, 1990, v. 79, n. 1, p. 130
By:
- Degiorgi, L.;
- Habeshaw, J. A.;
- Povey, S.;
- Matossian-Rogers, A.
Publication type:
Article
The changing challenges of nomenclature.
Published in:
Cytogenetics & Cell Genetics, 1999, v. 86, n. 2, p. 162, doi. 10.1159/000015372
By:
- Wain, H.;
- White, J.;
- Povey, S.
Publication type:
Article
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
Published in:
Annals of Human Genetics, 1999, v. 63, n. 1, p. 1
By:
- VALENTE, E. M.;
- POVEY, S.;
- WARNER, T. T.;
- WOOD, N. W.;
- DAVIS, M. B.
Publication type:
Article
A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.
Published in:
Annals of Human Genetics, 1998, v. 62, n. 3, p. 203, doi. 10.1046/j.1469-1809.1998.6230203.x
By:
- YOUNG, J. M.;
- BURLEY, M. W.;
- JEREMIAH, S. J.;
- JEGANATHAN, D.;
- EKONG, R.;
- OSBORNE, J. P.;
- POVEY, S.
Publication type:
Article
The effect of energy trade-offs on life history and fitness in the rice weevil, Sitophilus oryzae
Published in:
Oikos, 1992, v. 64, n. 3, p. 441, doi. 10.2307/3545159
By:
- Povey, S. R.;
- Holloway, G. J.
Publication type:
Article
Evolution in toxin-stressed environments
Published in:
Functional Ecology, 1990, v. 4, n. 3, p. 289
By:
- Sibly, R. M.;
- Holloway, G. J.;
- Povey, S. R.
Publication type:
Article
Establishment of a lymphoid cell line from leukemic cells of a patient with chronic lymphocytic leukemia.
Published in:
International Journal of Cancer, 1980, v. 26, n. 5, p. 551, doi. 10.1002/ijc.2910260505
By:
- Karande, A.;
- Fialkow, P. J.;
- Nilsson, K.;
- Povey, S.;
- Klein, G.;
- Najfeld, V.;
- Penfold, G.
Publication type:
Article
Somatic cell hybrids between human lymphoma lines. IV. Establishment and characterization of a p3HR-1/daudi hybrid.
Published in:
International Journal of Cancer, 1978, v. 21, n. 6, p. 707, doi. 10.1002/ijc.2910210607
By:
- Ber, R.;
- Klein, G.;
- Moar, M.;
- Rosén, A.;
- Westman, A.;
- Yefenof, E.;
- Povey, S.;
- Zeuthen, J.
Publication type:
Article
Production by EBV infection of an EBNA-positive subline from an EBNA-negative human lymphoma cell line without detectable EBV DNA.
Published in:
International Journal of Cancer, 1975, v. 16, n. 1, p. 125, doi. 10.1002/ijc.2910160114
By:
- Clements, G. B.;
- Klein, G.;
- Povey, S.
Publication type:
Article
Recommendations for locus-specific databases and their curation.
Published in:
Human Mutation, 2008, v. 29, n. 1, p. 2, doi. 10.1002/humu.20650
By:
- Cotton, R.G.H.;
- Auerbach, A.D.;
- Beckmann, J.S.;
- Blumenfeld, O.O.;
- Brookes, A.J.;
- Brown, A.F.;
- Carrera, P.;
- Cox, D.W.;
- Gottlieb, B.;
- Greenblatt, M.S.;
- Hilbert, P.;
- Lehvaslaiho, H.;
- Liang, P.;
- Marsh, S.;
- Nebert, D.W.;
- Povey, S.;
- Rossetti, S.;
- Scriver, C.R.;
- Summar, M.;
- Tolan, D.R.
Publication type:
Article
Combination therapy for HIV: the effect on inpatient activity, morbidity and mortality of a cohort of patients.
Published in:
1998
By:
- Brettle, Ray P.;
- Wilson, Alan;
- Povey, Sarah;
- Morris, Sheila;
- Morgan, Rhoda;
- Leen, Clifford L. S.;
- Hutchinson, Sharon;
- Lewis, Steff;
- Gore, Sheila;
- Brettle, R P;
- Wilson, A;
- Povey, S;
- Morris, S;
- Morgan, R;
- Leen, C L;
- Hutchinson, S;
- Lewis, S;
- Gore, S
Publication type:
journal article
Clinical features of AIDS in the Edinburgh City Hospital cohort.
Published in:
1996
By:
- Brettle, Raymond P.;
- Foreman, Angus;
- Povey, Sarah;
- Brettle, R P;
- Foreman, A;
- Povey, S
Publication type:
journal article
Further Data on Mitochondrial Malic Enzyme in Man.
Published in:
Human Heredity, 1978, v. 28, n. 6, p. 421, doi. 10.1159/000152993
By:
- Saha, N.;
- Jeremiah, S.J.;
- Povey, S.
Publication type:
Article

Found: 21

Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome.

cDNA and Genomic Clones Encoding the Human Muscle Acetylcholine Receptor.

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset<sup>a</sup>.

An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods<sup>a</sup>.

A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23<sup>a</sup>.

Characterisation of human cell lines and differentiation from HeLa by enzyme typing.

Fusion of rous-sarcoma-virus-transformed rat cells to morphologically normal human or rat cells results in transcriptional suppression of the provirus that depends on its chromosomal integration site.

Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: A study of 17 cases.

Reduction of graft-<em>versus</em>-host disease in neonatal F1 hybrid mice.

The changing challenges of nomenclature.

Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.

A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.

The effect of energy trade-offs on life history and fitness in the rice weevil, Sitophilus oryzae

Evolution in toxin-stressed environments

Establishment of a lymphoid cell line from leukemic cells of a patient with chronic lymphocytic leukemia.

Somatic cell hybrids between human lymphoma lines. IV. Establishment and characterization of a p3HR-1/daudi hybrid.

Production by EBV infection of an EBNA-positive subline from an EBNA-negative human lymphoma cell line without detectable EBV DNA.

Recommendations for locus-specific databases and their curation.

Combination therapy for HIV: the effect on inpatient activity, morbidity and mortality of a cohort of patients.

Clinical features of AIDS in the Edinburgh City Hospital cohort.

Further Data on Mitochondrial Malic Enzyme in Man.