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1 - 25 of 46 results for author:"McPherson J."Drop in Literature Citations

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Single nucleotide polymorphism-mediated translational suppression of endoplasmic reticulum mannosidase I modifies the onset of end-stage liver disease in alpha1-antitrypsin deficiency.

Pan S., Huang L., McPherson J., Muzny D., Rouhani F., Brantly M., Gibbs R., Sifers R.N.

Hepatology 50:275-281(2009) · Mapped (10)

A role for Mus81 in the repair of chromium-induced DNA damage.

Tamblyn L., Li E., Sarras H., Srikanth P., Hande M.P., McPherson J.P.

Mutat. Res. 660:57-65(2009) · Mapped (1)

Essential role for Bclaf1 in lung development and immune system function.

McPherson J.P., Sarras H., Lemmers B., Tamblyn L., Migon E., Matysiak-Zablocki E., Hakem A., Azami S.A., Cardoso R., Fish J. et al.

Cell Death Differ. 16:331-339(2009) · Mapped (7)

Interplay between Np95 and Eme1 in the DNA damage response.

Mistry H., Gibson L., Yun J.W., Sarras H., Tamblyn L., McPherson J.P.

Biochem. Biophys. Res. Commun. 375:321-325(2008) · Mapped (8)

A role for Brca1 in chromosome end maintenance.

McPherson J.P., Hande M.P., Poonepalli A., Lemmers B., Zablocki E., Migon E., Shehabeldin A., Porras A., Karaskova J., Vukovic B. et al.

Hum. Mol. Genet. 15:831-838(2006) · Mapped (43)

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

Lalani S.R., Safiullah A.M., Fernbach S.D., Harutyunyan K.G., Thaller C., Peterson L.E., McPherson J.D., Gibbs R.A., White L.D., Hefner M. et al.

Am. J. Hum. Genet. 78:303-314(2006) · UniProtKB (2) · Mapped (2)

Glucose-dependent insulinotropic polypeptide receptor knockout mice have altered bone turnover.

Xie D., Cheng H., Hamrick M., Zhong Q., Ding K.H., Correa D., Williams S., Mulloy A., Bollag W., Bollag R.J. et al.

Bone 37:759-769(2005) · Mapped (1)

Folic acid supplementation for 3 wk reduces pulse pressure and large artery stiffness independent of MTHFR genotype.

Williams C., Kingwell B.A., Burke K., McPherson J., Dart A.M.

Am. J. Clin. Nutr. 82:26-31(2005) · Mapped (9)

Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M. et al.

Nature 434:724-731(2005) · UniProtKB (4,275)

Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution.

Hillier L.W., Miller W., Birney E., Warren W., Hardison R.C., Ponting C.P., Bork P., Burt D.W., Groenen M.A.M., Delany M.E. et al.

Nature 432:695-716(2004) · UniProtKB (10)

Lats2/Kpm is required for embryonic development, proliferation control and genomic integrity.

McPherson J.P., Tamblyn L., Elia A., Migon E., Shehabeldin A., Matysiak-Zablocki E., Lemmers B., Salmena L., Hakem A., Fish J. et al.

EMBO J. 23:3677-3688(2004) · UniProtKB (1) · Mapped (14)

Involvement of mammalian Mus81 in genome integrity and tumor suppression.

McPherson J.P., Lemmers B., Chahwan R., Pamidi A., Migon E., Matysiak-Zablocki E., Moynahan M.E., Essers J., Hanada K., Poonepalli A. et al.

Science 304:1822-1826(2004) · UniProtKB (1)

Collaboration of Brca1 and Chk2 in tumorigenesis.

McPherson J.P., Lemmers B., Hirao A., Hakem A., Abraham J., Migon E., Matysiak-Zablocki E., Tamblyn L., Sanchez-Sweatman O., Khokha R. et al.

Genes Dev. 18:1144-1153(2004) · Mapped (20)

Genome sequence of the Brown Norway rat yields insights into mammalian evolution.

Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., Scott G., Steffen D., Worley K.C., Burch P.E. et al.

Nature 428:493-521(2004) · UniProtKB (351) · Mapped (82)

Levodopa-responsive aromatic L-amino acid decarboxylase deficiency.

Chang Y.T., Sharma R., Marsh J.L., McPherson J.D., Bedell J.A., Knust A., Braeutigam C., Hoffmann G.F., Hyland K.

Ann. Neurol. 55:435-438(2004) · UniProtKB (1) · Mapped (5)

A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.

Rao C., Foernzler D., Loftus S.K., Liu S., McPherson J.D., Jungers K.A., Apte S.S., Pavan W.J., Beier D.R.

Development 130:4665-4672(2003) · UniProtKB (1) · Mapped (7)

The DNA sequence of human chromosome 7.

Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R. et al.

Nature 424:157-164(2003) · UniProtKB (1)

The DNA sequence of human chromosome 7.

Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R. et al.

Nature 424:157-164(2003) · UniProtKB (2,635)

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.

Skaletsky H., Kuroda-Kawaguchi T., Minx P.J., Cordum H.S., Hillier L.W., Brown L.G., Repping S., Pyntikova T., Ali J., Bieri T. et al.

Nature 423:825-837(2003) · UniProtKB (115)

The DNA sequence and analysis of human chromosome 14.

Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A. et al.

Nature 421:601-607(2003) · UniProtKB (543)

Initial sequencing and comparative analysis of the mouse genome.

Waterston R.H., Lindblad-Toh K., Birney E., Rogers J., Abril J.F., Agarwal P., Agarwala R., Ainscough R., Alexandersson M., An P. et al.

Nature 420:520-562(2002) · UniProtKB (1)

Loss of Brca2 and p53 synergistically promotes genomic instability and deregulation of T-cell apoptosis.

Cheung A.M., Hande M.P., Jalali F., Tsao M.S., Skinnider B., Hirao A., McPherson J.P., Karaskova J., Suzuki A., Wakeham A. et al.

Cancer Res. 62:6194-6204(2002) · Mapped (14)

Brcal required for T cell lineage development but not TCR loci rearrangement.

Mak T.W., Hakem A., McPherson J.P., Shehabeldin A., Zablocki E., Migon E., Duncan G.S., Bouchard D., Wakeham A., Cheung A. et al.

Nat. Immunol. 1:77-82(2000) · Mapped (18)

Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval.

Simmons A.D., Puschel A.W., McPherson J.D., Overhauser J., Lovett M.

Biochem. Biophys. Res. Commun. 242:685-691(1998) · UniProtKB (1) · Mapped (5)

Allelic fusion of DNA topoisomerase II alpha and retinoic acid receptor alpha genes in adriamycin-resistant p388 murine leukemia revealed by fluorescence in situ hybridization.

Squire J.A., McPherson J.P., Beatty B.G., Goldenberg G.J.

Cytogenet. Cell Genet. 75:164-166(1996) · Mapped (11)

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