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12 documents found
1: Title: Gene-Based Genome-Wide Association Analysis in European and Asian Populations Identified Novel Genes for Rheumatoid Arthritis.
Authors: Zhu, Hong, et.al. .
Journal: PloS one, Vol. 11 (11): e0167212, 2016 .
Snippet: Among them, 105 genes had significant differential expressions between RA patients and health controls at least in one dataset, especially for 20 genes including 11 'overlapped' (ABCF1, FLOT1, HLA-F, IER3, TUBB, ZKSCAN4, BTN3A3, HSP90AB1, CUTA, BRD2, HLA-DMA), 5 'European-specific' (PHTF1, RPS18, BAK1, TNFRSF14, SUOX) and 4 'Asian-specific' (RNASET2, HFE, BTN2A2, MAPK13) genes whose differential expressions were significant at least in three datasets.
Affiliation: Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University, Suzhou, Jiangsu, China. Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, Soochow University, Suzhou, Jiangsu, China. Department of Child and Adolescent Health, School of Public Health, Medical College of Soochow University, Suzhou, Jiangsu, China. Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America. .
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2: Title: Association Studies of the GPR103 and BCL2L15 Genes in Autoimmune Thyroid Disease in the Japanese Population.
Authors: Ban, Yoshiyuki, et.al. .
Journal: Frontiers in endocrinology (Unknown Journal), Vol. 7, 2016 .
Snippet: While the past genome-wide association study (GWAS) for autoimmune thyroid diseases (AITDs) was done in Caucasians, a recent GWAS in Caucasian patients with both AITD and type 1 diabetes [a variant of autoimmune polyglandular syndrome type 3 (APS3v)] identified five non-HLA genes: BCL2L15, MAGI3, PHTF1, PTPN22, and GPR103.
Affiliation: Third Department of Internal Medicine, Teikyo University Chiba Medical Center , Ichihara , Chiba, Japan. Department of Pharmacogenomics, Showa University School of Pharmacy , Tokyo , Japan. .
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3: Title: Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors.
Authors: Caswell, Jennifer L, et.al. .
Journal: Human molecular genetics (Hum Mol Genet), Vol. 24 (25): 7421-31, 2015 .
Snippet: Six SNPs were associated with differential transcript expression of seven nearby genes at FDR < 0.05 (BABAM1, DCLRE1B/PHTF1, PEX14, RAD51L1, SRGAP2D and STXBP4).
Affiliation: Department of Medicine, Institute for Human Genetics, Helen Diller Family Comprehensive Cancer Center and, Department of Medicine, Division of Medical Oncology, Stanford University, Stanford, CA, USA and caswell@stanford.edu. Department of Medicine, Helen Diller Family Comprehensive Cancer Center and, Department of Cell and Tissue Biology, University of California, San Francisco, CA, USA. Department of Medicine, Institute for Human Genetics, Helen Diller Family Comprehensive Cancer Center and. Department of Plant and Microbial Biology, University of California, Berkeley, CA, USA. Department of Medicine, Institute for Human Genetics. .
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4: Title: Analysis of the expression of PHTF1 and related genes in acute lymphoblastic leukemia.
Authors: Huang, Xin, et.al. .
Journal: Cancer cell international (Unknown Journal), Vol. 15, 2015 .
Snippet: BACKGROUND: Previous study showed that downregulated BCL11B expression in T cell acute lymphoblastic leukemia (T-ALL) cell line Molt-4 inhibited cell proliferation and induce apoptosis, which may be related to PHTF1 gene overexpression.
Affiliation: Southern Medical University, 510515 Guangzhou, People's Republic of China ; Department of Haematology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, 510080 Guangzhou, People's Republic of China. Department of Haematology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, 510080 Guangzhou, People's Republic of China. Institute of Hematology, Medical College, Jinan University, 510632 Guangzhou, People's Republic of China. Institute of Hematology, Medical College, Jinan University, 510632 Guangzhou, People's Republic of China ; Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University, 510632 Guangzhou, People's Republic of China. .
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5: Title: LADA and T1D in Estonian population - two different genetic risk profiles.
Authors: Kisand, Kalle, et.al. .
Journal: Gene, Vol. 497 (2): 285-91, 2012 .
Snippet: METHODS: An ethnically homogenous population of Estonian origin, including 65 LADA patients, 154 patients with T1D, 260 patients with T2D and 229 non-diabetic controls, was genotyped for polymorphisms/haplotypes in HLA-DQB1, insulin gene (rs689, rs3842729), PHTF1-PTPN22 region (rs2476601, rs6679677), CTLA4 region (rs231806, rs16840252, rs5742909, rs231775, rs3087243, rs2033171), ICOS region (rs10932037, rs4675379), CD25 (rs706778), CD226(rs763361), NAA25 (rs17696736).
Affiliation: University of Tartu, Estonia. kalle.kisand@ut.ee .
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6: Title: Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population.
Journal: BMC medical genetics (Bmc Med Genet), Vol. 11, 2010 .
Snippet: CONCLUSIONS: The current study supports the rs6679677 (PHTF1-PTPN22), rs17696736 (C12orf30) and rs763361 (CD226) SNPs as susceptibility factors for type 1 diabetes outside the major histocompatibility region (MHC) region.
Affiliation: Immunology group, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia. drkmb@email.com .
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7: Title: Delineation of a 1Mb breakpoint region at 1p13 in Wilms tumors by fine-tiling oligonucleotide array CGH.
Authors: Natrajan, Rachael, et.al. .
Journal: Genes, chromosomes & cancer (Gene Chromosome Canc), Vol. 46 (6): 607-15, 2007 .
Snippet: The use of a 10 bp-spaced platform revealed that all four tumors in fact harbored different breakpoints, which targeted intragenic sequences in PHTF1, DCLRE1B, and NRAS, and an intergenic region immediately downstream of TRIM33.
Affiliation: Paediatric Oncology, Institute of Cancer Research/Royal Marsden NHS Trust, Sutton, UK. .
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8: Title: Putative homeodomain transcription factor 1 interacts with the feminization factor homolog fem1b in male germ cells.
Authors: Oyhenart, J, et.al. .
Journal: Biology of reproduction (Biol Reprod), Vol. 72 (4): 780-7, 2005 .
Snippet: The Phtf1 gene encodes a membrane protein abundantly expressed in male germinal cells.
Affiliation: INSERM U.567 CNRS-UMR 8104, Département d'Hématologie, Maternité de Port-Royal. .
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9: Title: Expression, regulation, and immunolocalization of putative homeodomain transcription factor 1 (PHTF1) in rodent epididymis: evidence for a novel form resulting from proteolytic cleavage.
Authors: Oyhenart, J, et.al. .
Journal: Biology of reproduction (Biol Reprod), Vol. 72 (1): 50-7, 2005 .
Snippet: PHTF1 is an 84-86-kDa membrane protein found in the endoplasmic reticulum of male germ cells in rodents.
Affiliation: INSERM U 567 CNRS-UMR 8104, Institut Cochin, Département d'Hématologie, Maternité de Port-Royal, Université René Descartes, 75014 Paris, France. .
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10: Title: Phtf1 is an integral membrane protein localized in an endoplasmic reticulum domain in maturing male germ cells.
Authors: Oyhenart, J, et.al. .
Journal: Biology of reproduction (Biol Reprod), Vol. 68 (3): 1044-53, 2003 .
Snippet: By using both ER and Golgi markers (TGN-38, p58), we were able to show that, in pachytene spermatocytes and in Golgi phase spermatids, phtf1 labeled a region neighboring the cis-Golgi that probably corresponded to the peripheral Golgi region.
Affiliation: INSERM U.567 CNRS-UMR 8104, Institut Cochin, Departement d'Hematologie, Maternité de Port-Royal, Université Rene Descartes, 75014 Paris, France. .
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11: Title: Molecular characterization of a novel gene family (PHTF) conserved from Drosophila to mammals.
Authors: Manuel, A, et.al. .
Journal: Genomics, Vol. 64 (2): 216-20, 2000 .
Snippet: PHTF1 (putative homeodomain transcriptional factor; HGMW-approved symbol PHTF1) is a putative homeobox gene located at band 1p11-p13 of the human genome.
Affiliation: INSERM U.474, Créteil, 94010, France. .
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12: Title: PHTF, a novel atypical homeobox gene on chromosome 1p13, is evolutionarily conserved.
Authors: Raich, N, et.al. .
Journal: Genomics, Vol. 59 (1): 108-9, 1999 .
No Abstract available.
Affiliation: Hôpital Henri Mondor, Créteil, 94010, France. Raich@infobiogen.fr .
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