Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells

Translating dosage compensation to trisomy 21

(2013) Jun Jiang et al.   NATURE

Induced pluripotent stem cells from patients with human fibrodysplasia ossificans progressiva show increased mineralization and cartilage formation

(2013) Yoshihisa Matsumoto et al.   Orphanet Journal of Rare Diseases

Genome damage in induced pluripotent stem cells: Assessing the mechanisms and their consequences

(2012) Samer M. I. Hussein et al.   BIOESSAYS

Unique Genomic Structure and Distinct Mitotic Behavior of Ring Chromosome 21 in Two Unrelated Cases

(2012) H.Z. Zhang et al.   CYTOGENETIC AND GENOME RESEARCH

Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array

(2011) Thomas J. Hoffmann et al.   GENOMICS

A more efficient method to generate integration-free human iPS cells

(2011) Keisuke Okita et al.   NATURE METHODS

Ring chromosome instability evaluation in six patients with autosomal rings

(2010) C.P. Sodr et al.   GENETICS AND MOLECULAR RESEARCH

Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis

(2010) Mary Ellen Moynahan et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Lissencephaly: Mechanistic insights from animal models and potential therapeutic strategies

(2010) Anthony Wynshaw-Boris et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling

(2009) Vaidehi Jobanputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Chromosome instability is common in human cleavage-stage embryos

(2009) Evelyne Vanneste et al.   NATURE MEDICINE

Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier

(2009) Anna Mantzouratou et al.   Molecular Cytogenetics

Protocols for cytogenetic studies of human embryonic stem cells

(2008) L MEISNER et al.   METHODS

Recurrent chromosomal abnormalities in human embryonic stem cells

(2008) Claudia Spits et al.   NATURE BIOTECHNOLOGY

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE