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1 - 25 of 30 results for author:"Doggett N.A."Drop in Literature Citations

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Analysis of the neurotoxin complex genes in Clostridium botulinum A1-A4 and B1 strains: BoNT/A3, /Ba4 and /B1 clusters are located within plasmids.

Smith T.J., Hill K.K., Foley B.T., Detter J.C., Munk A.C., Bruce D.C., Doggett N.A., Smith L.A., Marks J.D., Xie G. et al.

PLoS ONE 2:E1271-E1271(2007) · UniProtKB (14,772)

The complete genome sequence of Bacillus thuringiensis Al Hakam.

Challacombe J.F., Altherr M.R., Xie G., Bhotika S.S., Brown N., Bruce D., Campbell C.S., Campbell M.L., Chen J., Chertkov O. et al.

J. Bacteriol. 189:3680-3681(2007) · UniProtKB (4,792)

A 360-kb interchromosomal duplication of the human HYDIN locus.

Doggett N.A., Xie G., Meincke L.J., Sutherland R.D., Mundt M.O., Berbari N.S., Davy B.E., Robinson M.L., Rudd M.K., Weber J.L. et al.

Genomics 88:762-771(2006) · UniProtKB (1) · Mapped (2)

Pathogenomic sequence analysis of Bacillus cereus and Bacillus thuringiensis isolates closely related to Bacillus anthracis.

Han C.S., Xie G., Challacombe J.F., Altherr M.R., Bhotika S.S., Bruce D., Campbell C.S., Campbell M.L., Chen J., Chertkov O. et al.

J. Bacteriol. 188:3382-3390(2006) · UniProtKB (10,807)

Two variants of MutS homolog hMSH5: prevalence in humans and effects on protein interaction.

Yi W., Wu X., Lee T.H., Doggett N.A., Her C.

Biochem. Biophys. Res. Commun. 332:524-532(2005) · Mapped (20)

The sequence and analysis of duplication-rich human chromosome 16.

Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al.

Nature 432:988-994(2004) · UniProtKB (638)

Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and identifies underlying candidate tumor suppressor genes in prostate cancer.

Watson J.E., Doggett N.A., Albertson D.G., Andaya A., Chinnaiyan A., van Dekken H., Ginzinger D., Haqq C., James K., Kamkar S. et al.

Oncogene 23:3487-3494(2004) · UniProtKB (1)

Loss of heterozygosity and internal tandem duplication mutations of the CBP gene are frequent events in human esophageal squamous cell carcinoma.

So C.K., Nie Y., Song Y., Yang G.Y., Chen S., Wei C., Wang L.D., Doggett N.A., Yang C.S.

Clin. Cancer Res. 10:19-27(2004) · Mapped (7)

Mouse MutS homolog 4 is predominantly expressed in testis and interacts with MutS homolog 5.

Her C., Wu X., Bailey S.M., Doggett N.A.

Mamm. Genome 12:73-76(2001) · UniProtKB (1) · Mapped (11)

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.

Daniels R.J., Peden J.F., Lloyd C., Horsley S.W., Clark K., Tufarelli C., Kearney L., Buckle V.J., Doggett N.A., Flint J. et al.

Hum. Mol. Genet. 10:339-352(2001) · UniProtKB (91)

Identification and characterization of the mouse MutS homolog 5: Msh5.

Her C., Wu X., Wan W., Doggett N.A.

Mamm. Genome 10:1054-1061(1999) · UniProtKB (1) · Mapped (8)

The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer.

Crawford J., Ianzano L., Savino M., Whitmore S., Cleton-Jansen A.-M., Settasatiani C., D'Apolito M., Seshadri R., Pronk J.C., Auerbach A.D. et al.

Genomics 56:90-97(1999) · UniProtKB (1)

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

Whitmore S.A., Settasatian C., Crawford J., Lower K.M., McCallum B., Seshadri R., Cornelisse C.J., Moerland E.W., Cleton-Jansen A.-M., Tipping A.J. et al.

Genomics 52:325-331(1998) · UniProtKB (2)

Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene.

Her C., Doggett N.A.

Genomics 52:50-61(1998) · UniProtKB (1) · Mapped (4)

Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.

Centra M., Memeo E., D'Apolito M., Savino M., Ianzano L., Notarangelo A., Liu J., Doggett N.A., Zelante L., Savoia A.

Genomics 51:463-467(1998) · UniProtKB (1)

Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.

Levran O., Doggett N.A., Auerbach A.D.

Hum. Mutat. 12:145-152(1998) · UniProtKB (1)

A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.

Filippova G.N., Lindblom A., Meincke L.J., Klenova E.M., Neiman P.E., Collins S.J., Doggett N.A., Lobanenkov V.V.

Genes Chromosomes Cancer 22:26-36(1998) · UniProtKB (1)

Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.

Schollen E., Pardon E., Heykants L., Renard J., Doggett N.A., Callen D.F., Cassiman J.J., Matthijs G.

Hum. Mol. Genet. 7:157-164(1998) · UniProtKB (1)

Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever.

Aksentijevich I., Centola M., Deng Z., Sood R., Balow J.E. Jr., Wood G., Zaks N., Mansfield E., Chen X., Eisenberg S. et al.

Cell 90:797-807(1997) · UniProtKB (1)

MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3).

Sobulo O.M., Borrow J., Tomek R., Reshimi S., Harden A., Schlegelberger B., Housman D., Doggett N.A., Rowley J.D., Zeleznik-Le N.J.

Proc. Natl. Acad. Sci. U.S.A. 94:8732-8737(1997) · UniProtKB (1)

Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3.

Giles R.H., Petrij F., Dauwerse H.G., den Hollander A.I., Lushnikova T., van Ommen G.J.B., Goodman R.H., Deaven L.L., Doggett N.A., Peters D.J.M. et al.

Genomics 42:96-114(1997) · UniProtKB (1)

Chromosomal localization of the human and mouse hyaluronan synthase genes.

Spicer A.P., Seldin M.F., Olsen A.S., Brown N., Wells D.E., Doggett N.A., Itano N., Kimata K., Inazawa J., McDonald J.A.

Genomics 41:493-497(1997) · Mapped (22)

The genomic organization of the Fanconi anemia group A (FAA) gene.

Ianzano L., D'Apolito M., Centra M., Savino M., Levran O., Auerbach A.D., Cleton-Jansen A.-M., Doggett N.A., Pronk J.C., Tipping A.J. et al.

Genomics 41:309-314(1997) · UniProtKB (1)

Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.

Mitchison H.M., Taschner P.E., Kremmidiotis G., Callen D.F., Doggett N.A., Lerner T.J., Janes R.B., Wallace B.A., Munroe P.B., O'Rawe A.M. et al.

Neuropediatrics 28:12-14(1997) · Mapped (1)

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

Mitchison H.M., Munroe P.B., O'Rawe A.M., Taschner P.E.M., de Vos N., Kremmidiotis G., Lensink I., Munk A.C., D'Arigo K.L., Anderson J.W. et al.

Genomics 40:346-350(1997) · UniProtKB (1)

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