Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CCL25[original query] |
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Donor single nucleotide polymorphism in the CCR9 gene affects the incidence of skin GVHD. Bone marrow transplantation 2010 Feb 45 (2): 363-9. Inamoto Y, Murata M, Katsumi A, Kuwatsuka Y, Tsujimura A, Ishikawa Y, Sugimoto K, Onizuka M, Terakura S, Nishida T, Kanie T, Taji H, Iida H, Suzuki R, Abe A, Kiyoi H, Matsushita T, Miyamura K, Kodera Y, Naoe |
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis. American journal of human genetics 2019 8 105 (3): 549-561. Bosticardo Marita, Yamazaki Yasuhiro, Cowan Jennifer, Giardino Giuliana, Corsino Cristina, Scalia Giulia, Prencipe Rosaria, Ruffner Melanie, Hill David A, Sakovich Inga, Yemialyanava Irma, Tam Jonathan S, Padem Nurcicek, Elder Melissa E, Sleasman John W, Perez Elena, Niebur Hana, Seroogy Christine M, Sharapova Svetlana, Gebbia Jennifer, Kleiner Gary Ira, Peake Jane, Abbott Jordan K, Gelfand Erwin W, Crestani Elena, Biggs Catherine, Butte Manish J, Hartog Nicholas, Hayward Anthony, Chen Karin, Heimall Jennifer, Seeborg Filiz, Bartnikas Lisa M, Cooper Megan A, Pignata Claudio, Bhandoola Avinash, Notarangelo Luigi |
Dissecting the contribution of single nucleotide polymorphisms in CCR9 and CCL25 genomic regions to the celiac disease phenotype. Journal of translational autoimmunity 2021 12 4 100128. Airaksinen Laura, Cerqueira Juliana Xm, Huhtala Heini, Saavalainen Päivi, Yohannes Dawit A, Mäki Markku, Kurppa Kalle, Kilpeläinen Elina, Shcherban Anastasia, Palotie Aarno, Kaukinen Katri, Lindfors Kat |
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