Anna Collin (Former)
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- 2022
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Mark
Parkinson's disease and multiple system atrophy patient iPSC-derived oligodendrocytes exhibit alpha-synuclein-induced changes in maturation and immune reactive properties
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- Contribution to journal › Article
- 2021
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Mark
TNF-α and α-synuclein fibrils differently regulate human astrocyte immune reactivity and impair mitochondrial respiration
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- Contribution to journal › Article
- 2020
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Mark
Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene
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- Contribution to journal › Article
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Mark
Human iPSC-Derived Hippocampal Spheroids : An Innovative Tool for Stratifying Alzheimer Disease Patient-Specific Cellular Phenotypes and Developing Therapies
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- Contribution to journal › Article
- 2019
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Mark
Generation of an induced pluripotent stem cell line (CSC-46) from a patient with Parkinson's disease carrying a novel p.R301C mutation in the GBA gene
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- Contribution to journal › Article
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Mark
Cellular alterations identified in pluripotent stem cell-derived midbrain spheroids generated from a female patient with progressive external ophthalmoplegia and parkinsonism who carries a novel variation (p.Q811R) in the POLG1 gene
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- Contribution to journal › Article
- 2018
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Mark
Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 gene
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- Contribution to journal › Article
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Mark
Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C > T and EX6 del) in the PARK2 gene
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- Contribution to journal › Article
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Mark
Generation of a human induced pluripotent stem cell line (CSC-40) from a Parkinson's disease patient with a PINK1 p.Q456X mutation
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- Contribution to journal › Article
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Mark
Generation of an integration-free induced pluripotent stem cell line (CSC-43J) from a patient with sporadic Parkinson's disease
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- Contribution to journal › Article
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Mark
Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's disease
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- Contribution to journal › Article
- 2013
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Mark
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.
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- Contribution to journal › Article
- 2012
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Mark
Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders
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- Contribution to journal › Article
- 2010
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Mark
dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome.
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- Contribution to journal › Article
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Mark
Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.
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- Contribution to journal › Article
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Mark
Characterization of an alternative transcript of the human CREB3L2 gene.
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- Contribution to journal › Article
- 2009
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Mark
Clinical Variability of Waardenburg-Shah Syndrome in Patients With Proximal 13q Deletion Syndrome Including the Endothelin-B Receptor Locus
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- Contribution to journal › Article
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Mark
False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.
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- Contribution to journal › Article
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Mark
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
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- Contribution to journal › Article
- 2008
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Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
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- Contribution to journal › Article
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Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
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- Contribution to journal › Article
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Mark
Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
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- Contribution to journal › Article
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Mark
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
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- Contribution to journal › Article
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Mark
Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area
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- Contribution to journal › Article
- 2007
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Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
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- Contribution to journal › Article
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Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
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- Contribution to journal › Article