Detail Nature Genetics vol. 44 no. 05 (May 2012) Bibliografi Bahasa: (EN )    ISSN: 1061-4036    Year:: 2012    Bulan: 05    Edisi: May 2012     Penerbit: Nature Publishing Group Jenis: Journal - ilmiah internasional [Lihat daftar eksemplar jurnal Nature Genetics] Ketersediaan Perpustakaan FK Nomor Panggil: N12.K.2012.01 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada     Lihat Detail Induk Artikel dalam koleksi ini Germline RAD51C mutations confer susceptibility to ovarian cancer, halaman 475–476 Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis, halaman 483–489 Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture, halaman 491–501 Genetics of gene expression in primary immune cells identifies cell type–specific master regulators and roles of HLA alleles, halaman 502–510 Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population, halaman 511 - 516 A genome-wide association study identifies three new risk loci for Kawasaki disease, halaman 517 - 521 Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis, halaman 522 - 525 A genome-wide association meta-analysis identifies new childhood obesity loci, halaman 526–531 Common variants at 12q15 and 12q24 are associated with infant head circumference, halaman 532 - 538 Common variants at 6q22 and 17q21 are associated with intracranial volume, halaman 539 - 544 Common variants at 12q14 and 12q24 are associated with hippocampal volume, halaman 545 - 551 Identification of common variants associated with human hippocampal and intracranial volumes, halaman 552 - 561 Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis, halaman 562 - 569 Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes , halaman 570 - 574 ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome, halaman 575–580 Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of a-dystroglycan, halaman 581–585 Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair, halaman 586 - 592 Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair, halaman 593 - 597 UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair, halaman 598 - 602 Bayesian method to predict individual SNP genotypes from gene expression data , halaman 603 - 608  Edit Artikel Lihat Sejarah Pengadaan  Konversi Metadata   Kembali

Copyright © 2006, 2007 Unika Atma Jaya, all rights reserved