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Milan Macek

Showing results (61-70 of 148) with videos related to

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Molecular Genetics and Genomics : MGG|May 14, 2024
Distribution of pathogenic variants in the CFTR gene in a representative cohort of people with cystic fibrosis in the Kingdom of BahrainOsama A Karim Majed, Fatema Osama Majed, Nabeel Jasim Almoamen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 8, 2011
Distribution of CFTR mutations in Eastern Hungarians: relevance to genetic testing and to the introduction of newborn screening for cystic fibrosisGergely Ivady, Laszlo Madar, Bela Nagy, et al.
Neuro Endocrinology Letters|November 19, 2016
Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosisMilan Hubacek, Tereza Kripnerova, Michaela Nemcikova, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 29, 2007
Detection of two Alu insertions in the CFTR geneJian-Min Chen, Emmanuelle Masson, Milan Macek, et al.
Journal of Community Genetics|March 15, 2017
Implementing genetic education in primary care: the Gen-Equip programmeMilena Paneque, Martina C Cornel, Vaclava Curtisova, et al.
Reproductive Biomedicine Online|March 14, 2017
Ovarian response to 150 µg corifollitropin alfa in a GnRH-antagonist multiple-dose protocol: a prospective cohort studyTamara Lerman, Marion Depenbusch, Askan Schultze-Mosgau, et al.
Scientific Reports|April 29, 2024
Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorderMartin Schwarz, Jan Geryk, Markéta Havlovicová, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern EuropeMarina Machatkova, Martina Brouckova, Milada Matejckova, et al.
Frontiers in Pharmacology|May 31, 2021
Enhanced Expression of Human Epididymis Protein 4 (HE4) Reflecting Pro-Inflammatory Status Is Regulated by CFTR in Cystic Fibrosis Bronchial Epithelial CellsZsolt Bene, Zsolt Fejes, Tibor Gabor Szanto, et al.
Genes|February 27, 2026
Prevalence of Smith-Lemli-Opitz Syndrome Carriers and the Spectrum of <i>DHCR7</i> Pathogenic Variants in Representative Czech and Hungarian Population CohortsEszter Kovács, Zsuzsanna Szűcs, Miroslav Horňák, et al.
Pageof 15

Showing results (61-70 of 148) with videos related to

Sort By:
Pageof 15
Molecular Genetics and Genomics : MGG|May 14, 2024
Distribution of pathogenic variants in the CFTR gene in a representative cohort of people with cystic fibrosis in the Kingdom of BahrainOsama A Karim Majed, Fatema Osama Majed, Nabeel Jasim Almoamen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 8, 2011
Distribution of CFTR mutations in Eastern Hungarians: relevance to genetic testing and to the introduction of newborn screening for cystic fibrosisGergely Ivady, Laszlo Madar, Bela Nagy, et al.
Neuro Endocrinology Letters|November 19, 2016
Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosisMilan Hubacek, Tereza Kripnerova, Michaela Nemcikova, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 29, 2007
Detection of two Alu insertions in the CFTR geneJian-Min Chen, Emmanuelle Masson, Milan Macek, et al.
Journal of Community Genetics|March 15, 2017
Implementing genetic education in primary care: the Gen-Equip programmeMilena Paneque, Martina C Cornel, Vaclava Curtisova, et al.
Reproductive Biomedicine Online|March 14, 2017
Ovarian response to 150 µg corifollitropin alfa in a GnRH-antagonist multiple-dose protocol: a prospective cohort studyTamara Lerman, Marion Depenbusch, Askan Schultze-Mosgau, et al.
Scientific Reports|April 29, 2024
Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorderMartin Schwarz, Jan Geryk, Markéta Havlovicová, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern EuropeMarina Machatkova, Martina Brouckova, Milada Matejckova, et al.
Frontiers in Pharmacology|May 31, 2021
Enhanced Expression of Human Epididymis Protein 4 (HE4) Reflecting Pro-Inflammatory Status Is Regulated by CFTR in Cystic Fibrosis Bronchial Epithelial CellsZsolt Bene, Zsolt Fejes, Tibor Gabor Szanto, et al.
Genes|February 27, 2026
Prevalence of Smith-Lemli-Opitz Syndrome Carriers and the Spectrum of <i>DHCR7</i> Pathogenic Variants in Representative Czech and Hungarian Population CohortsEszter Kovács, Zsuzsanna Szűcs, Miroslav Horňák, et al.
Pageof 15