Scientific Commons: S. A. Whitmore

Experimental Investigation of Base Drag Reduction on a Two-Dimensional Body Using Boundary Layer Manipulation. Meeting Paper AIAA-2004-904, Research Engineering, NASA Dryden Flight Research Center (2004)

Durgesh, V., Naughton, J. W., Whitmore, S. A.

An experimental study of a two-dimensional wedge model has been carried out to assess conditions under which increasing viscous fore-body drag reduces base drag. Pressure, shear stress, and hot-wire...

CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3 (2002)

Kochetkova, Marina, McKenzie, O. L., Bais, Anthony J., Martin, J. M., Secker, G. A., Seshadri, R., ...

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes (2002)

Powell, J. A., Gardner, A. E., Bais, A. J., Hinze, S. J., Baker, E. G., Whitmore, S. A., ...

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes (2002)

Powell, J. A., Gardner, A. E., Bais, Anthony J., Hinze, S. J., Baker, Elizabeth Gay, Whitmore, S. A., ...

Tumour Suppressor Gene (2002)

Callen, David Frederick, Whitmore, S. A., Kremmidiotis, G., Kochetkova, Marina, Crawford, J.

Publication Number: WO/2002/018592, Publication Date: 07.03.2002, Chapter 2 Demand Filed: 12.03.2002

Tumour Suppressor Gene Identified on Chromosome 18 (2002)

Callen, David Frederick, Whitmore, S. A., Kremmidiotis, G., Kochetkova, Marina, Crawford, J.

Publication Number: WO/2002/048354, Publication Date: 20.06.2002,

CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3 (2002)

Kochetkova, Marina, McKenzie, O. L., Bais, Anthony J., Martin, J. M., Secker, G. A., Seshadri, R., ...

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes (2002)

Powell, J. A., Gardner, A. E., Bais, Anthony J., Hinze, S. J., Baker, Elizabeth Gay, Whitmore, S. A., ...

Tumour Suppressor Gene (2002)

Callen, David Frederick, Whitmore, S. A., Kremmidiotis, G., Kochetkova, Marina, Crawford, J.

Publication Number: WO/2002/018592, Publication Date: 07.03.2002, Chapter 2 Demand Filed: 12.03.2002

Tumour Suppressor Gene Identified on Chromosome 18 (2002)

Callen, David Frederick, Whitmore, S. A., Kremmidiotis, G., Kochetkova, Marina, Crawford, J.

Publication Number: WO/2002/048354, Publication Date: 20.06.2002,

Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, M., Centra, M., Van Beerendonk, H. M., Cleton-Jansen, A. M., Whitmore, S. A., ...

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 (1999)

Settasatian, C., Whitmore, S. A., Crawford, J., Bilton, R. L., Cleton Jansen, A. M., Sutherland, G. R., ...

C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain (1999)

Bhalla, K., Eyre, H. J., Whitmore, S. A., Sutherland, G. R., Callen, D. F.

Characterisation of Copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, Maria, Centra, M., Van Beerendonk, H. M., Whitmore, S. A., ...

The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer (1999)

Crawford, J., Ianzano, L., Savino, M., Whitmore, S. A., Settasatian, C., ...

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 (1999)

Settasatian, C., Whitmore, S. A., Crawford, J., Bilton, R. L., Sutherland, G. R., ...

C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain (1999)

Bhalla, K., Eyre, H. J., Whitmore, S. A., Sutherland, G. R., Callen, D. F.

Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, M., Centra, M., Van Beerendonk, H. M., Cleton-Jansen, A. M., Whitmore, S. A., ...

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 (1999)

Settasatian, C., Whitmore, S. A., Crawford, J., Bilton, R. L., Cleton Jansen, A. M., Sutherland, G. R., ...

C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain (1999)

Bhalla, K., Eyre, H. J., Whitmore, S. A., Sutherland, G. R., Callen, D. F.

Characterisation of Copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, Maria, Centra, M., Van Beerendonk, H. M., Whitmore, S. A., ...

The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer (1999)

Crawford, J., Ianzano, L., Savino, M., Whitmore, S. A., Settasatian, C., ...

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 (1999)

Settasatian, C., Whitmore, S. A., Crawford, J., Bilton, R. L., Sutherland, G. R., ...

C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain (1999)

Bhalla, K., Eyre, H. J., Whitmore, S. A., Sutherland, G. R., Callen, D. F.

Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16 (1998)

Cavanaugh, J. A., Callen, D. F., Wilson, S. R., Stanford, P. M., Sraml, M. E., Gorska, M., ...

Characterization and Screening For Mutations of the Growth Arrest-Specific 11 (Gas11) and C16orf3 Genes At 16q24.3 in Breast Cancer (1998)

Whitmore, S. A., Settasatian, C., Crawford, J., Lower, K. M., McCallum, B., Seshadri, R., ...

Construction of a High-Resolution Physical and Transcription Map of Chromosome 16q24.3 - a Region of Frequent Loss of Heterozygosity in Sporadic Breast Cancer (1998)

Whitmore, S. A., Crawford, J., Apostolou, S., Eyre, H., Baker, E., Lower, K. M., ...

A Novel Gene Encoding an Integral Membrane Protein Is Mutated in Nephropathic Cystinosis (1998)

Town, M., Jean, G., Cherqui, S., Attard, M., Forestier, L., Whitmore, S. A., ...

Analysis of Australian Crohn's disease pedigrees refines the localisation for susceptibility to inflammatory bowel disease on chromosome 16. (1998)

Cavanaugh, J. A., Callen, D. F., Wilson, S. R., Stanford, P. M., Sraml, M. E., Gorska, M., ...

Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer. (1998)

Whitmore, S. A., Settasatian, C., Crawford, J., Lower, K. M., McCallum, B., Seshadri, R., ...

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer. (1998)

Whitmore, S. A., Crawford, J., Apostolou, S., Eyre, H. J., Baker, E., Lower, K., ...

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. (1998)

Town, M., Jean, G., Cherqui, S., Attard, M., Forestier, L., Whitmore, S. A., ...

Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16 (1998)

Cavanaugh, J. A., Callen, D. F., Wilson, S. R., Stanford, P. M., Sraml, M. E., Gorska, M., ...

Characterization and Screening For Mutations of the Growth Arrest-Specific 11 (Gas11) and C16orf3 Genes At 16q24.3 in Breast Cancer (1998)

Whitmore, S. A., Settasatian, C., Crawford, J., Lower, K. M., McCallum, B., Seshadri, R., ...

Construction of a High-Resolution Physical and Transcription Map of Chromosome 16q24.3 - a Region of Frequent Loss of Heterozygosity in Sporadic Breast Cancer (1998)

Whitmore, S. A., Crawford, J., Apostolou, S., Eyre, H., Baker, E., Lower, K. M., ...

A Novel Gene Encoding an Integral Membrane Protein Is Mutated in Nephropathic Cystinosis (1998)

Town, M., Jean, G., Cherqui, S., Attard, M., Forestier, L., Whitmore, S. A., ...

Analysis of Australian Crohn's disease pedigrees refines the localisation for susceptibility to inflammatory bowel disease on chromosome 16. (1998)

Cavanaugh, J. A., Callen, D. F., Wilson, S. R., Stanford, P. M., Sraml, M. E., Gorska, M., ...

Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer. (1998)

Whitmore, S. A., Settasatian, C., Crawford, J., Lower, K. M., McCallum, B., Seshadri, R., ...

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer. (1998)

Whitmore, S. A., Crawford, J., Apostolou, S., Eyre, H. J., Baker, E., Lower, K., ...

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. (1998)

Town, M., Jean, G., Cherqui, S., Attard, M., Forestier, L., Whitmore, S. A., ...

The Genomic Organization of the Fanconi Anemia Group A (FAA) Gene (1997)

Ianzano, L., Dapolito, M., Centra, M., Savino, M., Levran, O., Auerbach, A. D., ...

The genome organisation of the Fanconi Anemia Group A (FAA) Gene (1997)

Ianzano, L., D'Apolito, M., Centra, M., Savino, M., Levran, O., Auerbach, A. D., ...

The Genomic Organization of the Fanconi Anemia Group A (FAA) Gene (1997)

Ianzano, L., Dapolito, M., Centra, M., Savino, M., Levran, O., Auerbach, A. D., ...

The genome organisation of the Fanconi Anemia Group A (FAA) Gene (1997)

Ianzano, L., D'Apolito, M., Centra, M., Savino, M., Levran, O., Auerbach, A. D., ...

Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9 (1996)

Wang, Z. Y., Qiu, Q. Q., Seufert, W., Taguchi, T., Testa, J. R., Whitmore, S. A., ...

Positional cloning of the Fanconi anaemia group A gene (1996)

Apostolou, S., Whitmore, S A., Crawford, J., Lennon, G., Sutherland, G R., Callen, D F., ...

Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9 (1996)

Wang, Z. Y., Qiu, Q. Q., Seufert, W., Taguchi, T., Testa, J. R., Whitmore, S. A., ...

Positional cloning of the Fanconi anaemia group A gene (1996)

Apostolou, S., Whitmore, S A., Crawford, J., Lennon, G., Sutherland, G R., Callen, D F., ...

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12 (1995)

Callen, D. F., Lane, S. A., Kozman, H., Kremmidiotis, G., Whitmore, S. A., Lowenstein, M., ...

An integrated physical map of human chromosome 16 (1995)

Doggett, N. A., Goodwin, L. A., Tesmer, J. G., Meincke, L. J., Bruce, D. C., Clark, L. M., ...

We describe an integrated physical, genetic and cytogenetic map of human chromosome 16 comprising both a low-resolution megaYAC map and a high-resolution cosmid contig/mlnlYAC map, which provides...

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12 (1995)

Callen, D. F., Lane, S. A., Kozman, H., Kremmidiotis, G., Whitmore, S. A., Lowenstein, M., ...

An integrated physical map of human chromosome 16 (1995)

Doggett, N. A., Goodwin, L. A., Tesmer, J. G., Meincke, L. J., Bruce, D. C., Clark, L. M., ...

We describe an integrated physical, genetic and cytogenetic map of human chromosome 16 comprising both a low-resolution megaYAC map and a high-resolution cosmid contig/mlnlYAC map, which provides...

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12

Callen, D. F., Baker, E., Lane, S., Nancarrow, J., Thompson, A., Whitmore, S. A., ...

The gene for Batten disease (CLN3) has been mapped to human chromosome 16 by demonstration of linkage to the haptoglobin locus, and its localization has been further refined using a panel of DNA...

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12

Callen, D. F., Baker, E., Lane, S., Nancarrow, J., Thompson, A., Whitmore, S. A., ...

The gene for Batten disease (CLN3) has been mapped to human chromosome 16 by demonstration of linkage to the haptoglobin locus, and its localization has been further refined using a panel of DNA...

S. A. Whitmore

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