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Cell Discovery|January 23, 2024
Pharmacology of LRRK2 with type I and II kinase inhibitors revealed by cryo-EMHanwen Zhu, Patricia Hixson, Wen Ma, et al.
Blood|September 27, 2003
Unique CD18 mutations involving a deletion in the extracellular stalk region and a major truncation of the cytoplasmic domain in a patient with leukocyte adhesion deficiency type 1Patricia Hixson, C Wayne Smith, Susan B Shurin, et al.
Cell|June 9, 2021
Structural analysis of the full-length human LRRK2Alexander Myasnikov, Hanwen Zhu, Patricia Hixson, et al.
Cell Research|February 12, 2023
Human IFT-A complex structures provide molecular insights into ciliary transportMeiqin Jiang, Vivek Reddy Palicharla, Darcie Miller, et al.
Nucleic Acids Research|January 24, 2015
Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombinationMichał Startek, Przemyslaw Szafranski, Tomasz Gambin, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delayJens Witsch, Przemyslaw Szafranski, Chun-An Chen, et al.
BMC Biology|September 24, 2014
Human endogenous retroviral elements promote genome instability via non-allelic homologous recombinationIan M Campbell, Tomasz Gambin, Piotr Dittwald, et al.
The Journal of Molecular Diagnostics : JMD|August 21, 2010
Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogeneticsLina Shao, Sung-Hae L Kang, Jian Li, et al.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Human Genetics|August 15, 2012
Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilizationSvetlana A Yatsenko, Patricia Hixson, Erin K Roney, et al.
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