Search Results - "Hallast, P."

Fine-scale quantification of HCG beta gene transcription in human trophoblastic and non-malignant non-trophoblastic tissues by Rull, K., Hallast, P., Uusküla, L., Jackson, J., Punab, M., Salumets, A., Campbell, R.K., Laan, M.

“…Human chorionic gonadotropin (HCG) is produced by syncytiotrophoblast of placenta. It delays the apoptosis of corpus luteum and functions in implantation. Its…”
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The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades by Hallast, Pille, Batini, Chiara, Zadik, Daniel, Maisano Delser, Pierpaolo, Wetton, Jon H, Arroyo-Pardo, Eduardo, Cavalleri, Gianpiero L, de Knijff, Peter, Destro Bisol, Giovanni, Dupuy, Berit Myhre, Eriksen, Heidi A, Jorde, Lynn B, King, Turi E, Larmuseau, Maarten H, López de Munain, Adolfo, López-Parra, Ana M, Loutradis, Aphrodite, Milasin, Jelena, Novelletto, Andrea, Pamjav, Horolma, Sajantila, Antti, Schempp, Werner, Sears, Matt, Tolun, Aslıhan, Tyler-Smith, Chris, Van Geystelen, Anneleen, Watkins, Scott, Winney, Bruce, Jobling, Mark A

“…Many studies of human populations have used the male-specific region of the Y chromosome (MSY) as a marker, but MSY sequence variants have traditionally been…”
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Human Y Chromosome Exerts Pleiotropic Effects on Susceptibility to Atherosclerosis by Eales, James M, Maan, Akhlaq A, Xu, Xiaoguang, Michoel, Tom, Hallast, Pille, Batini, Chiara, Zadik, Daniel, Prestes, Priscilla R, Molina, Elsa, Denniff, Matthew, Schroeder, Juliane, Bjorkegren, Johan L.M, Thompson, John, Maffia, Pasquale, Guzik, Tomasz J, Keavney, Bernard, Jobling, Mark A, Samani, Nilesh J, Charchar, Fadi J, Tomaszewski, Maciej

“…OBJECTIVE:The male-specific region of the Y chromosome (MSY) remains one of the most unexplored regions of the genome. We sought to examine how the genetic…”
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Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin beta gene cluster by Hallast, Pille, Nagirnaja, Liina, Margus, Tõnu, Laan, Maris

“…Segmental duplicons (>1 kb) of high sequence similarity (>90%) covering >5% of the human genome are characterized by complex sequence variation. Apart from a…”
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NOVEL POLYMORPHIC ALUYB8 INSERTION IN WNK GENE ASSOCIATED WITH BLOOD PRESSURE REGULATION: PP.21.335 by Putku, M, Kepp, K, Org, E, Sõber, S, Comas, D, Viigimaa, M, Veldre, G, Kelgo, P, Hallast, P, Tõnisson, N, Juhanson, P, Khusnutdinova, E, Kozich, V, Laan, M

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Analysis of SNP profiles in patients with major depressive disorder by Kõks, Sulev, Nikopensius, Tiit, Koido, Kati, Maron, Eduard, Altmäe, Signe, Heinaste, Evelin, Vabrit, Kristel, Tammekivi, Veronika, Hallast, Pille, Kurg, Ants, Shlik, Jakov, Vasar, Veiko, Metspalu, Andres, Vasar, Eero

“…The present study focused on 91 single-nucleotide polymorphisms (SNPs) in 21 candidate genes to find associations with major depressive disorder (MDD). In…”
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Association study of 90 candidate gene polymorphisms in panic disorder by Maron, Eduard, Nikopensius, Tiit, Kõks, Sulev, Altmäe, Signe, Heinaste, Evelin, Vabrit, Kristel, Tammekivi, Veronika, Hallast, Pille, Koido, Kati, Kurg, Ants, Metspalu, Andres, Vasar, Eero, Vasar, Veiko, Shlik, Jakov

“…In the present investigation we screened a large number of single nucleotide polymorphisms in the genes relevant to the neurobiology of anxiety for their…”
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Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders by Koido, Kati, Kõks, Sulev, Nikopensius, Tiit, Maron, Eduard, Altmäe, Signe, Heinaste, Evelin, Vabrit, Kristel, Tammekivi, Veronika, Hallast, Pille, Kurg, Ants, Shlik, Jakov, Vasar, Veiko, Metspalu, Andres, Vasar, Eero

“…Wolfram syndrome gene (WFS1) has been suggested to have a role in the susceptibility for mood disorders. A 26-fold increased risk for psychiatric disorders in…”
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P.3.031 Association study of 90 candidategenetic polymorphisms in panic disorder: Positive findings with SNPs in serotonin, cholecystokinin and dopamine related genes by Maron, E., Nkopensius, T., Kõks, S., Altmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, P., Koido, K., Kurg, A., Metspalu, A., Vasar, E., Vasar, V., Shlik, J.

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