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THE BAN OF ASSOCIATION OF CROATIAN THEATRE VOLUNTEERS BY COMMUNIST AUTHORITIES IN CROATIA (1945 – 1947)

Revue für kroatische Geschichte = Revue d'histoire croate, 2019-12, Vol.XV (1), p.9

Bukvić, Nenad

2019

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The Continuous Adaptive Challenge Played by Arboviruses: An In Silico Approach to Identify a Possible Interplay between Conserved Viral RNA Sequences and Host RNA Binding Proteins (RBPs)

International journal of molecular sciences, 2023-07, Vol.24 (13), p.11051

2023

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An in silico pipeline approach uncovers a potentially intricate network involving spike SARS-CoV-2 RNA, RNA vaccines, host RNA-binding proteins (RBPs), and host miRNAs at the cellular level

Journal of Genetic Engineering and Biotechnology, 2022-12, Vol.20 (1), p.129, Article 129

2022

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Rising Roles of Small Noncoding RNAs in Cotranscriptional Regulation: In Silico Study of miRNA and piRNA Regulatory Network in Humans

Genes, 2020-04, Vol.11 (5), p.482

2020

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A SARS-CoV-2 host infection model network based on genomic human Transcription Factors (TFs) depletion

Heliyon, 2020-10, Vol.6 (10), p.e05010, Article e05010

2020

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In Silico Analysis of Possible Interaction between Host Genomic Transcription Factors (TFs) and Zika Virus (ZikaSPH2015) Strain with Combinatorial Gene Regulation; Virus Versus Host-The Game Reloaded

Pathogens (Basel), 2021-01, Vol.10 (1), p.69

2021

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An integration into the diagnostic workflow in a pediatric patient suspected of having Marfan syndrome

The Egyptian journal of medical human genetics, 2022-12, Vol.23 (1)

2022

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Pathogenic DNM1L Variant (1085G>A) Linked to Infantile Progressive Neurological Disorder: Evidence of Maternal Transmission by Germline Mosaicism and Influence of a Contemporary in cis Variant (1535T>C)

Genes, 2021-08, Vol.12 (9), p.1295

2021

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The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein

Genes, 2020-12, Vol.11 (12), p.1519

2020

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Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1

Genes, 2018-04, Vol.9 (4), p.216

2018

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The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate

Italian journal of pediatrics, 2020-05, Vol.46 (1), p.74-74, Article 74

2020

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Wider Action Plan and Multidisciplinar Approach Could Be a Wining Idea in Creation of Friendly Environment

Journal of Environmental and Public Health, 2012-01, Vol.2012, p.473427-7

2012

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A homozygous frameshift mutation in the ESCO2 gene: Evidence of intertissue and interindividual variation in Nmd efficiency

Journal of cellular physiology, 2006-10, Vol.209 (1), p.67-73

2006

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Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15

Pediatric neurology, 2009-07, Vol.41 (1), p.65-67

2009

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From clinical suspect to molecular confirmation of noonan syndrome; contribution of “best practice” genetic counseling and new technical possibilities

Genetika (Beograd), 2015, Vol.47 (3), p.877-884

2015

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Genetics in the art and art in genetics

Gene, 2015-01, Vol.555 (1), p.14-22

2015

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The Target Therapy Hyperbole: “KRAS (p.G12C)”—The Simplification of a Complex Biological Problem

Cancers, 2024-06, Vol.16 (13), p.2389

2024

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Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians

Mutation research, 2001-11, Vol.498 (1), p.159-167

2001

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First report of whole CFTR gene duplication in a healthy newborn carrying R74W and V855I variants on the same allele

Journal of cystic fibrosis, 2024-02

2024

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Detection of premature segregation of centromeres in persons exposed to ionizing radiation

Health physics (1958), 2010-05, Vol.98 (5), p.717

2010

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Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants

Journal of medical genetics, 2023-02, Vol.60 (2), p.163

2023

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E-savjetovanja o propisima i planskim dokumentima o javnoj arhivskoj službi u Hrvatskoj: analiza komentara

Arhivski vjesnik, 2022-12, Vol.65 (1), p.13-25

Bukvić, Nenad

2022

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THE BAN OF ASSOCIATION OF CROATIAN THEATRE VOLUNTEERS BY COMMUNIST AUTHORITIES IN CROATIA (1945 – 1947)

The Continuous Adaptive Challenge Played by Arboviruses: An In Silico Approach to Identify a Possible Interplay between Conserved Viral RNA Sequences and Host RNA Binding Proteins (RBPs)

An in silico pipeline approach uncovers a potentially intricate network involving spike SARS-CoV-2 RNA, RNA vaccines, host RNA-binding proteins (RBPs), and host miRNAs at the cellular level

Rising Roles of Small Noncoding RNAs in Cotranscriptional Regulation: In Silico Study of miRNA and piRNA Regulatory Network in Humans

A SARS-CoV-2 host infection model network based on genomic human Transcription Factors (TFs) depletion

What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis

In Silico Analysis of Possible Interaction between Host Genomic Transcription Factors (TFs) and Zika Virus (ZikaSPH2015) Strain with Combinatorial Gene Regulation; Virus Versus Host-The Game Reloaded

An integration into the diagnostic workflow in a pediatric patient suspected of having Marfan syndrome

Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer

Pathogenic DNM1L Variant (1085G>A) Linked to Infantile Progressive Neurological Disorder: Evidence of Maternal Transmission by Germline Mosaicism and Influence of a Contemporary in cis Variant (1535T>C)

The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein

Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1

The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate

Wider Action Plan and Multidisciplinar Approach Could Be a Wining Idea in Creation of Friendly Environment

A homozygous frameshift mutation in the ESCO2 gene: Evidence of intertissue and interindividual variation in Nmd efficiency

Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15

From clinical suspect to molecular confirmation of noonan syndrome; contribution of “best practice” genetic counseling and new technical possibilities

Genetics in the art and art in genetics

The Target Therapy Hyperbole: “KRAS (p.G12C)”—The Simplification of a Complex Biological Problem

Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians

First report of whole CFTR gene duplication in a healthy newborn carrying R74W and V855I variants on the same allele

Detection of premature segregation of centromeres in persons exposed to ionizing radiation

Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation

Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants

E-savjetovanja o propisima i planskim dokumentima o javnoj arhivskoj službi u Hrvatskoj: analiza komentara

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