Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Syndrome and TH[original query] |
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Alpha-particle carcinogenesis in Thorotrast patients: epidemiology, dosimetry, pathology, and molecular analysis. Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer 2002 1 20 (4): 311-5. Ishikawa Y, Wada I, Fukumoto |
VNTR polymorphism of tyrosine hydroxylase gene and schizophrenia in the Korean population. Neuropsychobiology 2003 47 (3): 131-6. Pae Chi-Un, Kim Jung-Jin, Serretti Alessandro, Lee Chang-Uk, Lee Soo-Jung, Lee Chul, Paik In- |
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits. Human molecular genetics 2004 Apr 13 (7): 715-25. Rodríguez Santiago, Gaunt Tom R, O'Dell Sandra D, Chen Xiao-He, Gu Dongfeng, Hawe Emma, Miller George J, Humphries Stephen E, Day Ian N |
Association between Antipsychotics-Induced Restless Legs Syndrome and Tyrosine Hydroxylase Gene Polymorphism. Psychiatry investigation 2009 Sep 6 (3): 3. Cho Chul-Hyun, Kang Seung-Gul, Choi Jung-Eun, Park Young-Min, Lee Heon-Jeong, Kim Le |
Polymorphism 1936A > G in the AKAP10 gene (encoding A-kinase-anchoring protein 10) is associated with higher cholesterol cord blood concentration in Polish full-term newsborns. Journal of perinatal medicine 2013 Mar 41 (2): 205-10. ?oniewska Beata, Kaczmarczyk Mariusz, Clark Jeremy Simon, Kordek Agnieszka, Ciechanowicz Andrz |
Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians. Journal of forensic sciences 2014 Nov 59 (6): 1650-3. Studer Jacqueline, Bartsch Christine, Haas Cordu |
A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations. BMC medical genetics 2015 16 21. Truszkowska Gra?yna T, Bili?ska Zofia T, Kosi?ska Joanna, ?leszycka Justyna, Rydzanicz Ma?gorzata, Sobieszcza?ska-Ma?ek Ma?gorzata, Franaszczyk Maria, Bili?ska Maria, Stawi?ski Piotr, Michalak Ewa, Ma?ek ?ukasz A, Chmielewski Przemys?aw, Foss-Nieradko Bogna, Machnicki Marcin M, Stok?osa Tomasz, Poni?ska Joanna, Szumowski ?ukasz, Grzybowski Jacek, Piwo?ski Jerzy, Drygas Wojciech, Zieli?ski Tomasz, P?oski Raf |
Thyroid function in Rett syndrome. Hormone research in paediatrics 2015 83 (2): 118-25. Stagi Stefano, Cavalli Loredana, Congiu Laura, Scusa Maria Flora, Ferlini Alessandra, Bigoni Stefania, Benincasa Alberto, Rossi Bruno, Pini Giorg |
Increased circulating interleukin-8 in patients with resistance to thyroid hormone receptor ?. Endocrine connections 2017 11 6 (8): 731-740. van der Spek Anne H, Surovtseva Olga V, Aan Saskia, Tool Anton T J, van de Geer Annemarie, Demir Korcan, van Gucht Anja L M, van Trotsenburg A S Paul, van den Berg Timo K, Fliers Eric, Boelen Ani |
Genetic Variations Associated with Sleep Disorders in Patients with Schizophrenia: A Systematic Review. Medicines (Basel, Switzerland) 2018 3 5 (2): . Assimakopoulos Konstantinos, Karaivazoglou Katerina, Skokou Maria, Kalogeropoulou Marina, Kolios Panagiotis, Gourzis Philippos, Patrinos George P, Tsermpini Evangelia Eiri |
Metabolic Syndrome in Inflammatory Bowel Disease: Association with Genetic Markers of Obesity and Inflammation. Metabolic syndrome and related disorders 2019 11 18 (1): 31-38. Dragasevic Sanja, Stankovic Biljana, Kotur Nikola, Sokic-Milutinovic Aleksandra, Milovanovic Tamara, Lukic Snezana, Milosavljevic Tomica, Srzentic Drazilov Sanja, Klaassen Kristel, Pavlovic Sonja, Popovic Drag |
Apparent resistance to thyroid hormones: From biological interference to genetics. Annales d'endocrinologie 2019 10 80 (5-6): 280-285. Dieu Xavier, Sueur Guillaume, Moal Valérie, Boux de Casson Florence, Bouzamondo Nathalie, Bouhours Natacha, Briet Claire, Illouz Frédéric, Reynier Pascal, Coutant Régis, Rodien Patrice, Mirebeau-Prunier Delphi |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome. BMC medical genetics 2020 2 21 (1): 21. Caffarelli Carla, Gonnelli Stefano, Pitinca Maria Dea Tomai, Camarri Silvia, Al Refaie Antonella, Hayek Joussef, Nuti Ranucc |
In-Silico and In-Vitro Analysis of Human SOS1 Protein Causing Noonan Syndrome - A Novel Approach to Explore the Molecular Pathways. Current genomics 2022 4 22 (7): 526-540. Sigamani Vinoth, Rajasingh Sheeja, Gurusamy Narasimman, Panda Arunima, Rajasingh Johns |
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- Page last updated:Apr 22, 2024
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