Paweł Gawliński

发表

Complex interplay between the length and composition of the huntingtin-derived peptides modulates the intracellular behavior of the N-terminal fragments of mutant huntingtin.

D. Bąk, J. Bal, P. Gawliński, 2015, European journal of cell biology.

Why Functional Pre-Erythrocytic and Bloodstage Malaria Vaccines Fail: A Meta-Analysis of Fully Protective Immunizations and Novel Immunological Model

D. L. Guilbride, P. Gawliński, P. Guilbride, 2010, PloS one.

Malaria's deadly secret: a skin stage.

D. L. Guilbride, P. Gawliński, P. Guilbride, 2012, Trends in parasitology.

Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5

C. Walsh, E. Yang, A. Barkovich, 2020, Neuron.

Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects

A. Szczepankiewicz, A. Materna-Kiryluk, D. Larysz, 2022, Frontiers in Molecular Biosciences.

Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital Microcephaly

E. Obersztyn, E. Jamroz, W. Wiszniewski, 2021, Genes.

De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser–Winter Syndrome

M. Dawidziuk, M. Bekiesińska-Figatowska, A. Kutkowska-Kaźmierczak, 2022, International journal of molecular sciences.

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.

P. Striano, M. Fornerod, N. Brunetti‐Pierri, 2019, American journal of human genetics.

A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly

R. Durak, S. Bartoszewski, P. Podlasz, 2022, Cells.

Comprehensive genomic analysis of patients with disorders of cerebral cortical development

J. Lupski, R. Gibbs, E. Boerwinkle, 2018, European Journal of Human Genetics.

Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene

E. Obersztyn, R. Płoski, W. Wiszniewski, 2021, Genes.

The MED13L Haploinsufficiency Syndrome Associated with De Novo Nonsense Variant (P.GLN1981*)

R. Płoski, W. Wiszniewski, M. Rydzanicz, 2020, Journal of mother and child.

Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations.

V. Narayanan, N. Orenstein, J. Giltay, 2024, Cell death & disease.