HuGE Literature Finder
Records 1-11
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.
Carcinogenesis 2020 05 41 (3): 284-295. Avitabile Marianna, Succoio Mariangela, Testori Alessandro, Cardinale Antonella, Vaksman Zalman, Lasorsa Vito Alessandro, Cantalupo Sueva, Esposito Matteo, Cimmino Flora, Montella Annalaura, Formicola Daniela, Koster Jan, Andreotti Virginia, Ghiorzo Paola, Romano Maria Fiammetta, Staibano Stefania, Scalvenzi Massimiliano, Ayala Fabrizio, Hakonarson Hakon, Corrias Maria Valeria, Devoto Marcella, Law Matthew H, Iles Mark M, Brown Kevin, Diskin Sharon, Zambrano Nicola, Iolascon Achille, Capasso Mar |
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Relationships between plasma lactate, plasma alanine, genetic variations in lactate transporters and type 2 diabetes in the Japanese population.
Drug metabolism and pharmacokinetics 2019 Oct . Higuchi Issei, Kimura Yuki, Kobayashi Masaki, Narumi Katsuya, Furugen Ayako, Miyoshi Hideaki, Nakamura Akinobu, Yamada Takehiro, Atsumi Tatsuya, Iseki K |
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Variants in MCT10 protein do not affect FT3 levels in athyreotic patients.
Endocrine 2019 Jul . Cantara S, Ricci C, Maino F, Marzocchi C, Pacini F, Castagna M |
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BSG and MCT1 Genetic Variants Influence Survival in Multiple Myeloma Patients.
Genes 2018 Apr 9 (5): . ?acina Piotr, Butrym Aleksandra, Mazur Grzegorz, Bogunia-Kubik Katarzy |
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Associations of common variants in the SLC16A11, TCF7L2, and ABCA1 genes with pediatric-onset type 2 diabetes and related glycemic traits in families: A case-control and case-parent trio study.
Pediatric diabetes 2017 Jan . Miranda-Lora América L, Cruz Miguel, Molina-Díaz Mario, Gutiérrez Jorge, Flores-Huerta Samuel, Klünder-Klünder Migu |
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Ontogeny of ABC and SLC transporters in the microvessels of developing rat brain.
Fundamental & clinical pharmacology 2015 Dec . Soares Ricardo V, Do Tuan M, Mabondzo Aloïse, Pons Gérard, Chhun Stéphan |
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High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2015 Oct jc20152763. Rozenkova Klara, Malikova Jana, Nessa Azizun, Dusatkova Lenka, Bjørkhaug Lise, Obermannova Barbora, Dusatkova Petra, Kytnarova Jitka, Aukrust Ingvild, Najmi Laeya, Rypackova Blanka, Sumnik Zdenek, Lebl Jan, Njølstad Pål R, Hussain Khalid, Pruhova Stepan |
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Monocarboxylate transporter 1 deficiency and ketone utilization.
The New England journal of medicine 2014 Nov 371 (20): 1900-7. van Hasselt Peter M, Ferdinandusse Sacha, Monroe Glen R, Ruiter Jos P N, Turkenburg Marjolein, Geerlings Maartje J, Duran Karen, Harakalova Magdalena, van der Zwaag Bert, Monavari Ardeshir A, Okur Ilyas, Sharrard Mark J, Cleary Maureen, O'Connell Nuala, Walker Valerie, Rubio-Gozalbo M Estela, de Vries Maaike C, Visser Gepke, Houwen Roderick H J, van der Smagt Jasper J, Verhoeven-Duif Nanda M, Wanders Ronald J A, van Haaften Gi |
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Clinical and Molecular Characterisation of 300 patients with Congenital Hyperinsulinism.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Jan . Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K |
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Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2012 Dec . Snider KE, Becker S, Boyajian L, Shyng SL, Macmullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A |
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Genetic variations in the MCT1 (SLC16A1) gene in the Chinese population of Singapore.
Drug metabolism and pharmacokinetics 2009 24 (5): 469-74. Lean Choo Bee, Lee Edmund Jon Deo |
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- Page last updated:Mar 05, 2021
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