J. Paděrová

发表

Murine Pif1 Interacts with Telomerase and Is Dispensable for Telomere Function In Vivo

J. Squire, B. Snow, A. Wakeham, 2006, Molecular and Cellular Biology.

Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization.

J. Squire, J. Bayani, G. Maire, 2007, Cancer genetics and cytogenetics.

Plk4 is required for cytokinesis and maintenance of chromosomal stability

J. Dennis, A. Pollett, J. Squire, 2010, Proceedings of the National Academy of Sciences.

Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes

M. Turnovec, Miroslava Balaščáková, J. Čopíková, 2020, Annals of human genetics.

The breakage–fusion–bridge (BFB) cycle as a mechanism for generating genetic heterogeneity in osteosarcoma

J. Squire, J. Bayani, G. Maire, 2006, Chromosoma.

Epigenetic and Phenotypic Consequences of a Truncation Disrupting the Imprinted Domain on Distal Mouse Chromosome 7

L. Lefebvre, J. Squire, M. Gertsenstein, 2007, Molecular and Cellular Biology.

Prospective and parallel assessments of cystic fibrosis newborn screening protocols in the Czech Republic: IRT/DNA/IRT versus IRT/PAP and IRT/PAP/DNA

M. Macek, Miroslava Balaščáková, T. Piskáčková, 2012, European Journal of Pediatrics.

Integrated Cytogenetic and High-Resolution Array CGH Analysis of Genomic Alterations Associated with MYCN Amplification

J. Squire, J. Bayani, A. Pandita, 2011, Cytogenetic and Genome Research.

The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region.

L. Lefebvre, J. Squire, M. Gertsenstein, 2009, Human molecular genetics.

Title: Epigenetic and Phenotypic Consequences of a Truncation Disrupting the Imprinted 2 Domain on Distal Mouse Chromosome 7 3 4 Running Title: Genomic Imprinting from a Truncated Chromosome 5

L. Lefebvre, J. Squire, M. Gertsenstein, 2022 .

Prkar1a is an osteosarcoma tumor suppressor that defines a molecular subclass in mice.

T. Triche, P. Hu, S. Molyneux, 2010, The Journal of clinical investigation.

Novel 6p rearrangements and recurrent translocation breakpoints in retinoblastoma cell lines identified by spectral karyotyping and mBAND analyses.

B. Gallie, G. da Cunha Santos, J. Squire, 2007, Cancer genetics and cytogenetics.

Under the mask of Kabuki syndrome: Elucidation of genetic-and phenotypic heterogeneity in patients with Kabuki-like phenotype.

M. Macek, V. Moslerová, M. Havlovicová, 2018, European journal of medical genetics.

High definition cytogenetics and oligonucleotide aCGH analyses of cisplatin‐resistant ovarian cancer cells

A. Tsalenko, A. Ben-Dor, M. Barrett, 2007, Genes, chromosomes & cancer.

Distinct patterns of structural and numerical chromosomal instability characterize sporadic ovarian cancer.

B. Rosen, J. Squire, J. Bayani, 2008, Neoplasia.

Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK.

T. Kalina, V. Kanderova, O. Hrusak, 2021, The Journal of allergy and clinical immunology.

Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring

M. Macek, A. Maver, M. Havlovicová, 2016, Clinical genetics.

SD-OCT imaging as a valuable tool to support molecular genetic diagnostics of Usher syndrome type 1.

J. Čopíková, P. Lišková, L. Dudakova, 2018, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Baroreflex Sensitivity in Children, Adolescents, and Young Adults with Essential and White-Coat Hypertension

B. Fiser, P. Balcárková, J. Paděrová, 2005, Klinische Padiatrie.