[Twins in nature, science, and society]

In vitro evaluation and biodistribution of HER2-targeted liposomes loaded with an (125)I-labelled DNA-intercalator.

Journal of drug targeting·2011

Epidermal growth factor-DNA conjugate for two-step targeting.

International journal of oncology·2011

Oncolytic adenovirus modified with somatostatin motifs for selective infection of neuroendocrine tumor cells.

Gene therapy·2011

Hsp90 is expressed and represents a therapeutic target in human oesophageal cancer using the inhibitor 17-allylamino-17-demethoxygeldanamycin.

British journal of cancer·2009

Astatinated trastuzumab, a putative agent for radionuclide immunotherapy of ErbB2-expressing tumours.

Oncology reports·2006

Identification and characterization of a novel splicing variant of vesicular monoamine transporter 1.

Journal of molecular endocrinology·2005

Prevalence and forms of congenital anomalies in twins born in Pomeranian District during the period from 1.07.1997 to 31.12.1998. Polish Register of Congenital Anomalies.

Acta geneticae medicae et gemellologiae·2000

Analysis of triple test results in 27 cases of twin pregnancies.

Acta geneticae medicae et gemellologiae·2000

Long-term follow-up study of somatic development in prematurely born twins after life-threatening episodes.

Acta geneticae medicae et gemellologiae·2000

Ultrasound in the diagnosis of twin-to-twin transfusion syndrome--a preliminary report.

Acta geneticae medicae et gemellologiae·2000

From the research on electrophoretical mobility of nuclei in twins.

Acta geneticae medicae et gemellologiae·2000

Neurodevelopmental dysfunction and specific learning disabilities in school-aged twins.

Acta geneticae medicae et gemellologiae·2000

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

The Plant journal : for cell and molecular biology·2026

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

The Journal of infectious diseases·2026

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[Twins in nature, science, and society]

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In vitro evaluation and biodistribution of HER2-targeted liposomes loaded with an (125)I-labelled DNA-intercalator.

Epidermal growth factor-DNA conjugate for two-step targeting.

Oncolytic adenovirus modified with somatostatin motifs for selective infection of neuroendocrine tumor cells.

Hsp90 is expressed and represents a therapeutic target in human oesophageal cancer using the inhibitor 17-allylamino-17-demethoxygeldanamycin.

Astatinated trastuzumab, a putative agent for radionuclide immunotherapy of ErbB2-expressing tumours.

Identification and characterization of a novel splicing variant of vesicular monoamine transporter 1.

Prevalence and forms of congenital anomalies in twins born in Pomeranian District during the period from 1.07.1997 to 31.12.1998. Polish Register of Congenital Anomalies.

Analysis of triple test results in 27 cases of twin pregnancies.

Long-term follow-up study of somatic development in prematurely born twins after life-threatening episodes.

Ultrasound in the diagnosis of twin-to-twin transfusion syndrome--a preliminary report.

From the research on electrophoretical mobility of nuclei in twins.

Neurodevelopmental dysfunction and specific learning disabilities in school-aged twins.

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

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