Bibliotecas PUC-SP - Busca Integrada

Allan Award Introduction: Arthur L. Beaudet

Por Lupski, James R.
Publicado em 2008

Genomic Disorders: Recombination-Based Disease Resulting from Genome Architecture

Por Lupski, James R.
Publicado em 2003

Axonal Charcot-Marie-Tooth Disease and the Neurofilament Light Gene (NF-L)

Por Lupski, James R.
Publicado em 2000

Hotspots of homologous recombination in the human genome: not all homologous sequences are equal

Por Lupski, James R
Publicado em 2004

Genomic disorders ten years on

Por Lupski, James R
Publicado em 2009

Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes

Por Lupski, James R, Stankiewicz, Pawel
Publicado em 2005

Penetrance of Craniofacial Anomalies in Mouse Models of Smith-Magenis Syndrome Is Modified by Genomic Sequence Surrounding Rai1: Not All Null Alleles Are Alike

Por Yan, Jiong, Bi, Weimin, Lupski, James R.
Publicado em 2007

Animal models for human contiguous gene syndromes and other genomic disorders

Por Walz, Katherina, Fonseca, Patricia, Lupski, James R.
Publicado no Genetics and Molecular Biology (2004)

Copy number variation at the breakpoint region of isochromosome 17q

Por Carvalho, Claudia M.B., Lupski, James R.
Publicado em 2008

Mechanisms for human genomic rearrangements

Por Gu, Wenli, Zhang, Feng, Lupski, James R
Publicado em 2008

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

Por Hastings, P. J., Ira, Grzegorz, Lupski, James R.
Publicado em 2009

Genetic Proof of Unequal Meiotic Crossovers in Reciprocal Deletion and Duplication of 17p11.2

Por Shaw, Christine J., Bi, Weimin, Lupski, James R.
Publicado em 2002

Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates

Por Shaw, Christine J., Withers, Marjorie A., Lupski, James R.
Publicado em 2004

The Evolutionary Chromosome Translocation 4;19 in Gorilla gorilla is Associated with Microduplication of the Chromosome Fragment Syntenic to Sequences Surrounding the Human Proxima...

Por Stankiewicz, Pawel, Park, Sung-Sup, Inoue, Ken, Lupski, James R.
Publicado em 2001

A Chromosomal Rearrangement Hotspot Can Be Identified from Population Genetic Variation and Is Coincident with a Hotspot for Allelic Recombination

Por Lindsay, Sarah J., Khajavi, Mehrdad, Lupski, James R., Hurles, Matthew E.
Publicado em 2006

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)

Por Walz, Katherina, Paylor, Richard, Yan, Jiong, Bi, Weimin, Lupski, James R.
Publicado em 2006

Reply to Boylan

Por Wise, Carol A., Garcia, Carlos A., Patel, Pragna I., Lupski, James R.
Publicado em 1994

AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12

Por Babcock, Melanie, Yatsenko, Svetlana, Stankiewicz, Pawel, Lupski, James R., Morrow, Bernice E.
Publicado em 2007

Localization of mariner DNA Transposons in the Human Genome by PRINS

Por Reiter, Lawrence T., Liehr, Thomas, Rautenstrauss, Bernd, Robertson, Hugh M., Lupski, James R.
Publicado em 1999

Serial segmental duplications during primate evolution result in complex human genome architecture

Por Stankiewicz, Paweł, Shaw, Christine J., Withers, Marjorie, Inoue, Ken, Lupski, James R.
Publicado em 2004