Publications by authors named "Inna Inashkina"

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Mitochondrial cardiomyopathy with skeletal muscle myopathy caused by m.3260A > G mutation in MT-TL1 gene: a case report.
Anda Kadiša, Ritvars Vereskuns, Mihails Tarasovs, Ieva Mičule, Inna Inashkina

J Med Case Rep· November 2025

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Generation of induced pluripotent stem cell lines from three LGMD R1 patients carrying CAPN3 hypomorphic intronic variant c.1746-20C > G.
Karina Goluba, Vadims Parfejevs, Anastasija Neimane, Anastasija Tvoronovica, Baiba Lace, Inna Inashkina

Stem Cell Res· September 2025

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Genetic Analysis of and Other Anterior Segment Dysgenesis-Associated Genes in Latvian Cohort of Primary Congenital Glaucoma.
Eva Elksne, Baiba Lace, Janis Stavusis, Anastasija Tvoronovica, Pawel Zayakin, Inna Inashkina

Biomedicines· May 2025

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The phenotypic spectrum of deficiency.
Baiba Lace, Eissa Faqeih, Namik Kaya, Zita Krumina, Johannes A Mayr, Inna Inashkina

JIMD Rep· September 2024

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Self-organisation of early stress response in the biology of cancer.
Jekaterina Erenpreisa, Kristine Salmina, Ninel M Vainshelbaum, Inna Inashkina, Talivaldis Freivalds

Postepy Biochem· May 2024

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Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease.
Min-Yu Lan, Tsu-Kung Lin, Baiba Lace, Algirdas Utkus, Birute Burnyte, Inna Inashkina

Cells· April 2024

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Altered Splicing of in a Multigenerational Family from Latvia Affected by Danon Disease.
Janis Stavusis, Ieva Micule, Ieva Grinfelde, Anna Zdanovica, Janis Pudulis, Inna Inashkina

Medicina (Kaunas)· January 2024

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The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer.
Jekaterina Erenpreisa, Ninel Miriam Vainshelbaum, Marija Lazovska, Roberts Karklins, Kristine Salmina, Inna Inashkina

Int J Mol Sci· July 2023

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The Role of Mitotic Slippage in Creating a "Female Pregnancy-like System" in a Single Polyploid Giant Cancer Cell.
Kristine Salmina, Ninel Miriam Vainshelbaum, Madara Kreishmane, Inna Inashkina, Mark Steven Cragg

Int J Mol Sci· February 2023

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Impact of the m.13513G>A Variant on the Functions of the OXPHOS System and Cell Retrograde Signaling.
Dita Kidere, Pawel Zayakin, Diana Livcane, Marina Makrecka-Kuka, Janis Stavusis, Inna Inashkina

Curr Issues Mol Biol· February 2023

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CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related.
Magdalena Mroczek, Inna Inashkina, Janis Stavusis, Pawel Zayakin, Andrey Khrunin

Hum Mutat· October 2022

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Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia.
Baiba Lace, Ieva Micule, Viktorija Kenina, Signe Setlere, Jurgis Strautmanis, Inna Inashkina

Neurol Genet· June 2022

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Case Report: Two Families With Related Neurodegeneration.
Ieva Micule, Baiba Lace, Nathan T Wright, Nicolas Chrestian, Jurgis Strautmanis, Inna Inashkina

Front Genet· February 2022

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Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study.
Baiba Lace, Sander Pajusalu, Diana Livcane, Ieva Grinfelde, Ilze Akota, Inna Inashkina

Front Genet· February 2022

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Differentiating cancer cells reveal early large-scale genome regulation by pericentric domains.
Jekabs Krigerts, Kristine Salmina, Talivaldis Freivalds, Pawel Zayakin, Felikss Rumnieks, Inna Inashkina

Biophys J· February 2021

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The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants.
Ieva Malniece, Adele Grasmane, Inna Inashkina, Janis Stavusis, Madara Kreile

Am J Case Rep· July 2020

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Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicity.
Janis Stavusis, Ieva Micule, Nathan T Wright, Volker Straub, Ana Topf, Inna Inashkina

Neuromuscul Disord· June 2020

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"Mitotic Slippage" and Extranuclear DNA in Cancer Chemoresistance: A Focus on Telomeres.
Kristine Salmina, Agnieszka Bojko, Inna Inashkina, Karolina Staniak, Magdalena Dudkowska

Int J Mol Sci· April 2020

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DNA methylation of the Oct4A enhancers in embryonal carcinoma cells after etoposide treatment is associated with alternative splicing and altered pluripotency in reversibly senescent cells.
Mikhail Baryshev, Inna Inashkina, Kristine Salmina, Anda Huna, Thomas R Jackson

Cell Cycle· September 2019

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Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases.
Yoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Baratang, Praveen K Raju, Alexej Knaus, Inna Inashkina

Am J Hum Genet· August 2019

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Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy.
Janis Stavusis, Baiba Lace, Jochen Schäfer, Janelle Geist, Inna Inashkina

Ann Neurol· July 2019

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Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome.
Dita Pelnena, Birute Burnyte, Eriks Jankevics, Baiba Lace, Evelina Dagyte, Inna Inashkina

Mitochondrial DNA A DNA Mapp Seq Anal· October 2018

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Microbiome symbionts and diet diversity incur costs on the immune system of insect larvae.
Indrikis A Krams, Sanita Kecko, Priit Jõers, Giedrius Trakimas, Didzis Elferts, Inna Inashkina

J Exp Biol· November 2017

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A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene.
Janis Stavusis, Inna Inashkina, Baiba Lace, Dita Pelnena, Svetlana Limborska

Hum Hered· November 2017

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Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus.
Valentina Cipriani, Raquel S Silva, Gavin Arno, Nikolas Pontikos, Ambreen Kalhoro, Inna Inashkina

Sci Rep· August 2017

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