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Chrzanowska, Krystyna H
145  Ergebnisse:
Personensuche X
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1

Impaired p53-Mediated DNA Damage Response Contributes to Mi..:

Martins, Soraia ; Erichsen, Lars ; Datsi, Angeliki...
Cells.  11 (2022)  5 - p. 802 , 2022
Link: https://doi.org/10.3390/..
 
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2

The NBN founder mutation—Evidence for a country specific di..:

Chrzanowska, Krystyna H. ; Seemanova, Eva ; Varon, Raymonda...
Cancer Reports.  6 (2022)  2 - p. , 2022
Link: https://doi.org/10.1002/..
 
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3

Interfamilial clinical variability in four Polish families ..:

Walczak‐Sztulpa, Joanna ; Wawrocka, Anna ; Stańczyk, Małgorzata...
American Journal of Medical Genetics Part A.  185 (2021)  4 - p. 1195-1203 , 2021
Link: https://doi.org/10.1002/..
 
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4

The phenotype‐driven computational analysis yields clinical..:

Jezela‐Stanek, Aleksandra ; Ciara, Elżbieta ; Jurkiewicz, Dorota...
Molecular Genetics & Genomic Medicine.  8 (2020)  9 - p. , 2020
Link: https://doi.org/10.1002/..
 
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5

DNA damage and transcriptional regulation in iPSC-derived n..:

Corti, Alessandro ; Sota, Raina ; Dugo, Matteo...
Scientific Reports.  9 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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6

Genetic Spectrum of ABCA4-Associated Retinal Degeneration i..:

Tracewska, Anna M. ; Kocyła-Karczmarewicz, Beata ; Rafalska, Agnieszka...
Genes.  10 (2019)  12 - p. 959 , 2019
Link: https://doi.org/10.3390/..
 
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7

Fibroblast-derived integration-free iPSC line ISRM-NBS1 fro..:

Martins, Soraia ; Bohndorf, Martina ; Graffmann, Nina...
Stem Cell Research.  34 (2019)  - p. 101372 , 2019
Link: https://doi.org/10.1016/..
 
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8

Correction to: Circulating T Cells of Patients with Nijmege..:

Meijers, Ruud W. J. ; Dzierzanowska-Fangrat, Katarzyna ; Zborowska, Magdalena...
Journal of Clinical Immunology.  38 (2018)  4 - p. 538-538 , 2018
Link: https://doi.org/10.1007/..
 
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9

The germline variants in DNA repair genes in pediatric medu..:

Trubicka, Joanna ; Żemojtel, Tomasz ; Hecht, Jochen...
BMC Cancer.  17 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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10

Intrafamilial phenotypic variability in a Polish family wit..:

Walczak‐Sztulpa, Joanna ; Wawrocka, Anna ; Sobierajewicz, Agata...
American Journal of Medical Genetics Part A.  173 (2017)  5 - p. 1364-1368 , 2017
Link: https://doi.org/10.1002/..
 
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11

Additional data on the clinical phenotype of Helsmoortel—Va..:

Krajewska‐Walasek, Małgorzata ; Jurkiewicz, Dorota ; Piekutowska‐Abramczuk, Dorota...
American Journal of Medical Genetics Part A.  170 (2016)  6 - p. 1647-1650 , 2016
Link: https://doi.org/10.1002/..
 
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12

A novel TPM2 gene splice-site mutation causes severe congen..:

Mroczek, Magdalena ; Kabzińska, Dagmara ; Chrzanowska, Krystyna H...
Journal of Applied Genetics.  58 (2016)  2 - p. 199-203 , 2016
Link: https://doi.org/10.1007/..
 
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13

Circulating T Cells of Patients with Nijmegen Breakage Synd..:

Meijers, Ruud W. J. ; Dzierzanowska-Fangrat, Katarzyna ; Zborowska, Magdalena...
Journal of Clinical Immunology.  37 (2016)  2 - p. 133-142 , 2016
Link: https://doi.org/10.1007/..
 
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14

The Slavic NBN Founder Mutation: A Role for Reproductive Fi..:

Seemanova, Eva ; Varon, Raymonda ; Vejvalka, Jan...
PLOS ONE.  11 (2016)  12 - p. e0167984 , 2016
Link: https://doi.org/10.1371/..
 
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15

Diagnosis and management of Silver–Russell syndrome: first ..:

Wakeling, Emma L. ; Brioude, Frédéric ; Lokulo-Sodipe, Oluwakemi...
Nature Reviews Endocrinology.  13 (2016)  2 - p. 105-124 , 2016
Link: https://doi.org/10.1038/..
 
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