M. V. Van Keuren

发表

Simplified silver protein detection and image enhancement methods in polyacrylamide gels

C. Merril, D. Goldman, M. V. Van Keuren, 1982 .

DNA sequences surrounding the centromere of chromosome 21.

G. D. Stewart, D. Kurnit, M. V. Van Keuren, 1991, Cytogenetics and cell genetics.

Human chromosome 21-encoded cDNA clones.

G. D. Stewart, R. Neve, D. Patterson, 1986, Gene.

Assignment of the human slow twitch skeletal muscle/cardiac troponin C gene (TNNC1) to human chromosome 3p21.3-->3p14.3 using somatic cell hybrids.

J. Cypser, R. Gemmill, H. Drabkin, 1996, Cytogenetics and cell genetics.

Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesis.

D. Kurnit, Y. S. Chang, K. Buraczyńska, 1995, Cytogenetics and cell genetics.

Assignment of a third purine biosynthetic gene (glycinamide ribonucleotide transformylase) to human chromosome 21.

S. Benkovic, D. Patterson, H. Drabkin, 1986, American journal of human genetics.

Situs inversus in the developing mouse: Proteins affected by the iv mutation (genocopy) and the teratogen retinoic acid (phenocopy)

W. M. Layton, D. Kurnit, M. V. Van Keuren, 1991, Molecular reproduction and development.

Analysis of proteins expressed at the time of murine organogenesis

D. Kurnit, M. V. Van Keuren, R. A. Iacob, 1991, Molecular reproduction and development.

Rederivation of Transgenic and Gene-Targeted Mice by Embryo Transfer

T. Saunders, M. V. Van Keuren, 2004, Transgenic Research.

Resistance to organophosphorus agent toxicity in transgenic mice expressing the G117H mutant of human butyrylcholinesterase.

E. Duysen, O. Lockridge, T. Saunders, 2004, Toxicology and applied pharmacology.

The 724 family of DNA sequences is interspersed about the pericentromeric regions of human acrocentric chromosomes.

G. D. Stewart, R. Neve, G. Bruns, 1986, Cytogenetics and cell genetics.

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h.

X. Chen, J. Korenberg, J. Cheng, 1996, Genomics.

Protein variations associated with in vitro aging of human fibroblasts and quantitative limits on the error catastrophe hypothesis.

C. Merril, D. Goldman, M. V. Van Keuren, 1983, Journal of gerontology.

Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus.

P. S. St George-Hyslop, R. Tanzi, J. Gusella, 1987, Science.

Trace polypeptides in cellular extracts and human body fluids detected by two-dimensional electrophoresis and a highly sensitive silver stain.

C R Merril, C. Merril, R. Switzer, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Silver staining methods for polyacrylamide gel electrophoresis.

C. Merril, D. Goldman, M. V. Van Keuren, 1983, Methods in enzymology.

Molecular mechanism in the formation of a human ring chromosome 21.

S. Antonarakis, W. Earnshaw, G. Stetten, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Gel protein stains: silver stain.

C. Merril, D. Goldman, M. V. Van Keuren, 1984, Methods in enzymology.

Expression of the IV (reversed and/or heterotaxic) phenotype in SWV mice.

W. M. Layton, D. Kurnit, F. Biddle, 1993, Teratology.

Molecular structure of human chromosome 21.

G. D. Stewart, D. Kurnit, M. Buraczynska, 1989, Annual review of genetics.

Developmental appearance of proteins identified by two‐dimensional gel electrophoresis in mouse gonadal tissue

R. Erickson, D. Kurnit, E. J. Durbin, 1991, Molecular reproduction and development.

Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance.

D. Lashkari, J. Korenberg, D. Kurnit, 1996, Genome research.

Software aids for the analysis of 2D gel electrophoresis images.

M Schultz, P Lemkin, B Shapiro, 1979, Computers and biomedical research, an international journal.

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.

E. Jabs, J. Gusella, D. Patterson, 1986, American journal of human genetics.

Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes.

G. D. Stewart, R. Tanzi, J. Gusella, 1989, American journal of medical genetics.

Detection of radioactively labeled proteins is quenched by silver staining methods: quenching is minimal for 14C and partially reversible for 3H with a photochemical stain.

C. Merril, D. Goldman, M. V. Van Keuren, 1981, Analytical biochemistry.

A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.

R. Neve, G. Bruns, D. Patterson, 1987, Cytogenetics and cell genetics.

A Novel Intergenic ETnII-β Insertion Mutation Causes Multiple Malformations in Polypodia Mice

J. Nadeau, J. Lehoczky, A. Borowsky, 2013, PLoS genetics.

Amyloid β protein gene: cDNA, mRNA distribution and genetic linkage near the Alzheimer locus

R. Tanzi, J. Gusella, R. Neve, 1988 .

Analysis of proteins synthesized by 9.5 day mouse embryos: Determination of cardiac and noncardiac proteins

D. Kurnit, M. V. Van Keuren, R. Iacob, 1991, Molecular reproduction and development.

Transcription patterns of sequences on human chromosome 21.

Y. Jiang, D. Kurnit, E. Crombez, 1995, Cytogenetics and cell genetics.