M. Kapović

发表

Functional Polymorphisms of Matrix Metalloproteinases 1 and 9 Genes in Women with Spontaneous Preterm Birth

B. Peterlin, N. Tul, N. Pereza, 2014, Disease markers.

Mitochondrial DNA heritage of Cres Islanders--example of Croatian genetic outliers.

P. Rudan, R. Villems, E. Metspalu, 2009, Collegium antropologicum.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

B. Peterlin, S. Ristić, J. Sepčić, 2016, Neurological Sciences.

Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-&bgr; treatment response in multiple sclerosis patients: a preliminary report

B. Peterlin, O. Perković, S. Ristić, 2017, Pharmacogenetics and genomics.

Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis.

B. Peterlin, M. Volk, N. Pereza, 2016, Reproductive biomedicine online.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in lung cancer patients.

S. Ristić, M. Kapović, Veljko Flego, 2012, Genetic testing and molecular biomarkers.

Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion.

B. Peterlin, N. Pereza, M. Kapović, 2017, Fertility and sterility.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Body mass index, waist circumference and waist-to-hip ratio: which anthropometric indicator is better predictor for the hypertension development in women population of the island Cres.

B. Kolarić, N. Pereza, M. Kapović, 2012, Collegium antropologicum.

Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

S. Ristić, M. Kapović, N. Starčević Čizmarević, 2021, Physiological Research.

Hemochromatosis gene mutations in patients with alcoholic cirrhosis

B. Peterlin, D. S̆timac, S. Ristić, 2006, Clinical genetics.

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

B. Peterlin, D. S̆timac, S. Ristić, 2011, Medical science monitor : international medical journal of experimental and clinical research.

The Role of Iron and Iron Overload in Chronic Liver Disease

D. S̆timac, S. Ristić, L. Orlić, 2016, Medical science monitor : international medical journal of experimental and clinical research.

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.

B. Peterlin, M. Volk, N. Pereza, 2012, Reproductive biomedicine online.

Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion.

B. Peterlin, M. Volk, N. Pereza, 2013, Fertility and sterility.

BanI polymorphism of cytosolic phospholipase A2 gene is associated with age at onset in male patients with schizophrenia and schizoaffective disorder.

J. Giacometti, S. Nadalin, M. Kapović, 2008, Prostaglandins, leukotrienes, and essential fatty acids.

ORIGINAL ARTICLE: Genetic Predisposition to Idiopathic Recurrent Spontaneous Abortion: Contribution of Genetic Variations in IGF‐2 and H19 Imprinted Genes

B. Peterlin, M. Volk, N. Pereza, 2008, American journal of reproductive immunology.

A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses.

B. Peterlin, M. Volk, N. Pereza, 2015, Molecular human reproduction.

A current genetic and epigenetic view on human aging mechanisms.

N. Pereza, M. Kapović, S. Ostojić, 2009, Collegium Antropologicum.

Alloimmunization Against Well Defined Polymorphic Major Histocompatibility or Class I MHC Transfected L Cells Antigens Can Prevent Poly IC Induced Fetal Death in Mice

P. Kourilsky, C. Jaulin, G. Chaouat, 1995, American journal of reproductive immunology.

Hemochromatosis gene mutations in the Croatian and Slovenian populations

B. Peterlin, D. S̆timac, S. Ristić, 2003, Clinical genetics.

MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

B. Peterlin, O. Perković, S. Ristić, 2015, Journal of Neuroimmunology.

Frequency of CCR5 gene 32-basepair deletion in Croatian normal population.

S. Ristić, M. Kapović, N. Starčević Čizmarević, 2005, Croatian medical journal.

No association of CCR5D32 gene mutation with multiple sclerosis in Croatian and Slovenian patients

B. Peterlin, S. Ristić, L. Lovrečić, 2005, Multiple sclerosis.

Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor

S. Ristić, M. Kapović, Veljko Flego, 2013, Medical science monitor : international medical journal of experimental and clinical research.

The proportion of symmetric and asymmetric IgG antibody molecules synthesized by a cellular clone (hybridoma) can be regulated by placental culture supernatants.

G. Chaouat, M. Kapović, I. Borel, 1992, Cellular immunology.

Malignancy risk in patient with neurofibromatosis and autosomal dominant polycystic kidney disease.

M. Kapović, Veljko Flego, L. Zaputović, 2003, Croatian medical journal.

Elevated Second-Trimester Free β-hCG as an Isolated Finding and Pregnancy Outcomes

S. Ristić, M. Mimica, M. Kapović, 2004, Fetal Diagnosis and Therapy.

Sex-specific differences of craniofacial traits in Croatia: The impact of environment in a small geographic area

J. Giacometti, M. Kapović, S. Ostojić, 2007, Annals of human biology.

A Case of Lichen Ruber Planus in a Patient with Familial Multiple Sclerosis

B. Peterlin, O. Perković, S. Ristić, 2010, The Journal of international medical research.

Immuno-Endocrine Networks in Pregnancy

G. Chaouat, M. Kapović, J. Szekeres-Bartho, 1993 .

Chromosome Studies in Patients with Defective Reproductive Success

M. Kapović, ANĐELKA RADOJČIĆ BADOVINAC, ALENA BURETIĆ‐TOMLJANOVIĆ, 2000, American journal of reproductive immunology.

Complete Freund Adjuvant Treatment of Pregnant Females Influences Resorption Rates in CBA/J × DBA/2 Matings via Progesterone‐Mediated Immunomodulation

G. Chaouat, M. Kapović, J. Szekeres-Bartho, 1991, American journal of reproductive immunology.

Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review.

B. Peterlin, M. Volk, N. Pereza, 2013, Fertility and sterility.

The effects of microbiota abundance on symptom severity in Parkinson’s disease: A systematic review

B. Peterlin, G. Hauser, A. Kovanda, 2022, Frontiers in Aging Neuroscience.

Chromosomal Anomalies in Abnormal Human Pregnancies

S. Ristić, M. Kapović, O. Petrović, 1998, Fetal Diagnosis and Therapy.

CTLA‐4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

B. Peterlin, S. Ristić, J. Sepčić, 2011, International journal of immunogenetics.

Angiotensin‐converting enzyme I/D gene polymorphism and risk of multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2006, Acta neurologica Scandinavica.

Tumor Necrosis Factor-α-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients

B. Peterlin, S. Ristić, L. Lovrečić, 2007, European Neurology.

Genetics of recurrent spontaneous abortion: advances and controversies

B. Peterlin, N. Pereza, M. Kapović, 2016 .

Prenatal diagnosis of complete trisomy 19q

I. Babič, M. Kapović, O. Petrović, 2007, Prenatal diagnosis.

Third case of 8q23.3‐q24.13 deletion in a patient with Langer–Giedion syndrome phenotype without TRPS1 gene deletion

B. Peterlin, A. Maver, M. Volk, 2012, American journal of medical genetics. Part A.

Secular change of craniofacial measures in Croatian younger adults

M. Kapović, S. Ostojić, A. Buretić‐Tomljanović, 2006, American journal of human biology : the official journal of the Human Biology Council.

Lipid Classes and Fatty Acid Composition of Diplodus vulgaris and Conger conger Originating from the Adriatic Sea

Sanda Šulić, M. Kapović, J. Varljen, 2003 .

Potential Value of Hepatic Lipids from White Sea Bream (Diplodus sargus, L.) as a Good Source of Biomedical Components: Seasonal Variations

M. Kapović, Marta Žuvić Butorac, J. Varljen, 2009 .

LIVER AND MUSCLE TISSUE FATTY ACID COMPOSITION OF THE LIPID FRACTIONS OF DIPLODUS VULGARIS FROM THE NORTH ADRIATIC SEA, CROATIA

M. Kapović, J. Varljen, L. Batičić, 2005 .

Composition and seasonal variation of fatty acids of Diplodus vulgaris L. from the Adriatic Sea

M. Kapović, J. Varljen, L. Batičić, 2004 .

Polymorphisms in the Interleukin‐12/18 Genes and Recurrent Spontaneous Abortion

B. Peterlin, M. Volk, M. Kapović, 2007, American journal of reproductive immunology.

The Prevalence of Live Birth Down Syndrome in the Region of Primorsko-goranska County in Croatia, 1996–2005: The Impact of Screening and Amniocentesis

S. Ristić, G. Brumini, I. Prpić, 2008, Maternal and Child Health Journal.

The Influence of Smoking and Parity on Serum Markers for Down’s Syndrome Screening

S. Ristić, M. Petek, M. Kapović, 2002, Fetal Diagnosis and Therapy.

Altered LINE-1 Methylation in Mothers of Children with Down Syndrome

A. Stanković, M. Živković, M. Kapović, 2015, PloS one.

Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer.

S. Ristić, S. Nadalin, M. Kapović, 2020, Biomedical reports.

Pregnant women's attitudes toward amniocentesis before receiving Down syndrome screening results.

I. Babič, S. Ristić, G. Brumini, 2008, Women's health issues : official publication of the Jacobs Institute of Women's Health.

Screening for Down’s Syndrome and Neural Tube Defect in Croatia

S. Ristić, M. Kapović, V. Kosec, 1998, Fetal Diagnosis and Therapy.

Incidence of Down's syndrome in the municipality of Rijeka and Istrian region

M. Kapović, I. Medica, B. Brajenović-Milić, 1996 .

Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: Comments on the article by Pereza et al. [2012]

B. Peterlin, A. Maver, M. Volk, 2015, American journal of medical genetics. Part A.

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

B. Peterlin, A. Hodzic, S. Ristić, 2016, Brain and behavior.

The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients

S. Ristić, S. Nadalin, M. Kapović, 2017, Journal of Neural Transmission.

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

B. Peterlin, A. Maver, A. Hodzic, 2018, PloS one.

HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder

S. Ristić, M. Kapović, V. Šendula-Jengić, 2012, Molecular Biology Reports.

Angiotensin-converting enzyme gene polymorphism in patients with multiple sclerosis from Bosnia and Herzegovina.

B. Peterlin, S. Ristić, O. Sinanović, 2011, Genetic testing and molecular biomarkers.

Dupuytren's disease characteristics in Primorsko-goranska County, Croatia.

I. Kovic, I. Lulic, Davor Jurišić, 2008, Collegium antropologicum.

Functional Inference of Methylenetetrahydrofolate Reductase Gene Polymorphisms on Enzyme Stability as a Potential Risk Factor for Down Syndrome in Croatia

S. Ristić, M. Kapović, O. Petrović, 2010, Disease markers.

The effect of a compulsory curriculum on ethical attitudes of medical students.

S. Ristić, S. Vuletic, M. Kapović, 2000, Collegium antropologicum.

Influence of CCR5Δ32 gene mutation on interferon-beta treatment response in multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2015 .

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2015, Journal of Assisted Reproduction and Genetics.

Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p

I. Babič, M. Kapović, B. Brajenović-Milić, 2008, Cytogenetic and Genome Research.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Perception of arterial hypertension and myocardial infarction in hypertensive and normotensive men and women.

V. Mićović, M. Kapović, A. Ljubotina, 2011, Collegium antropologicum.

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2005, Neuroscience Letters.

Primary lung cancer and TNF-alpha gene polymorphisms: a case-control study in a Croatian population.

S. Ristić, M. Kapović, D. Matanić, 2009, Medical science monitor : international medical journal of experimental and clinical research.

The town of Cabar, Croatia, a high risk area for multiple sclerosis--analytic epidemiology of dietary factors.

O. Perković, A. Jurjević, I. Antončić, 2010, Collegium antropologicum.

Epidemiology of multiple sclerosis in western Herzegovina

B. Peterlin, S. Ristić, J. Sepčić, 2007, Clinical Neurology and Neurosurgery.

Genetic polymorphisms of 15 STR loci in the population of the island of Cres (Croatia)

P. Rudan, G. Lauc, Natalija Novokmet, 2011, Annals of human biology.

PAI and TPA gene polymorphisms in multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2008, Multiple sclerosis.

Maternal Serum Screening for Down Syndrome: A Survey of Pregnant Women’s Views

M. Kapović, B. Brajenović-Milić, Vlatka Jurcan, 2000, Public Health Genomics.

Human Y-specific STR haplotypes in the Western Croatian population sample.

B. Peterlin, S. Ristić, L. Lovrečić, 2005, Forensic science international.

Tumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients.

B. Peterlin, S. Ristić, L. Lovrečić, 2007, European Neurology.

The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis

B. Peterlin, O. Perković, S. Ristić, 2014, Disease markers.

Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans

B. Peterlin, D. Alavantic, S. Ristić, 2010, Multiple sclerosis.

Predictive parameters of gestational diabetes mellitus.

Ž. Crnčević-Orlić, S. Rački, M. Kapović, 2007, Collegium antropologicum.

The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion

B. Peterlin, A. Maver, M. Volk, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates

P. Rudan, M. Reidla, Erika Tamm, 2023, Genes.

Connection of depression and bone loss in perimenopausal and postmenopausal women.

Ana Orlić, Ž. Crnčević-Orlić, M. Kapović, 2012, Collegium antropologicum.

Genetic heritage of Croatians in the Southeastern European gene pool—Y chromosome analysis of the Croatian continental and Island population

P. Rudan, S. Rootsi, J. Šarac, 2016, American journal of human biology : the official journal of the Human Biology Council.

Lymphokines, cytokines and immunoregulators involved in pregnancy success or failure and perinatal AIDS

G. Chaouat, E. Menu, T. Wegmann, 1991 .

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2017, Journal of Assisted Reproduction and Genetics.

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.

B. Peterlin, M. Volk, N. Pereza, 2012, Reproductive biomedicine online.