A P Monaco

发表

Biohybrid artificial pancreas: long-term implantation studies in diabetic, pancreatectomized dogs.

B A Solomon, A. Monaco, T. Maki, 1991, Science.

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

Tomi D. Berney, E Maestrini, Stephen J. Guter, 2009, Molecular Psychiatry.

A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis

A. Monaco, A. Harding, A. Harding, 1996, Annals of neurology.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Successful treatment of diabetes with the biohybrid artificial pancreas in dogs.

B A Solomon, A. Monaco, T. Maki, 1991, Transplantation.

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA.

A. Monaco, H. Lehrach, Z. Larin, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Microinjection of neostigmine into the pontine reticular formation of cats enhances desynchronized sleep signs.

J A Hobson, J. Hobson, A. Monaco, 1984, The Journal of pharmacology and experimental therapeutics.

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

A. Monaco, C. Bertelson, L. Kunkel, 1988, Genomics.

Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

M Farrall, A Danek, A. Monaco, 1997, American journal of human genetics.

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.

A. Monaco, Y. Berwald‐Netter, A. Koulakoff, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Xenotransplantation of canine, bovine, and porcine islets in diabetic rats without immunosuppression.

B A Solomon, A. Monaco, R. Lanza, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins.

A. Monaco, R. Brasseur, F. Brasseur, 1997, Genomics.

Transplantation of islet allografts and xenografts in totally pancreatectomized diabetic dogs using the hybrid artificial pancreas.

A. Monaco, T. Maki, W. Chick, 1991, Annals of surgery.

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

G Baird, A. Bailey, G. Baird, 2002, American journal of human genetics.

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

M Bitner-Glindzicz, M. Bitner-Glindzicz, H. Ropers, 1995, Science.

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects

E Maestrini, E. Bacchelli, A. Bailey, 2005, Journal of Medical Genetics.

A gene-based genetic linkage and comparative map of the rat X chromosome.

E R Levy, G M Lathrop, A. Monaco, 1997, Genomics.

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

G Baird, C. Francks, G. Baird, 2014, Genes, brain, and behavior.

The utrophin and dystrophin genes share similarities in genomic structure.

A. Monaco, K. Davies, D. Blake, 1993, Human molecular genetics.

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.

A. Monaco, H. Lehrach, D. Nižetić, 1991, Proceedings of the National Academy of Sciences of the United States of America.