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811-820 trong số 897 kết quả
Mechanisms of Enhancer-Mediated Gene Activation in the Context of the 3D Genome
Tác giả: Argyris Papantonis, A Marieke Oudelaar
Xuất bản: United States: Annual review of genomics and human genetics , 2025
Bộ sưu tập: NCBI
ddc:  070.48346
 
Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliog...
Tác giả: David Haïm, Amale Achaiia, Tania Attié-Bitach, Nicolas Bourgon, Lucile Boutaud, Pierre Marijon, Candice Moncler, Chloé Quélin, Philippe Roth, Nathalie Roux, Sophie Thomas, Sarah Vanlieferinghen, Laure Verlin
Xuất bản: England: European journal of human genetics : EJHG , 2025
Bộ sưu tập: NCBI
ddc:  658.32259
 
Independent inheritance of cognition and bipolar disorder in a family sample
Tác giả: Alexander D'Amico, Nirmala Akula, Alejandro Arbona-Lampaya, Emily Besançon, Dwight Dickinson, Ally Freifeld, Joshua Garcia, Katie Hosey, Layla Kassem, Emma E M Knowles, Ley Lacbawan, Francis J McMahon, Heejong Sung
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  553.453
 
Reconsidering the Genetic Overlap Between Cognition and Bipolar Disorder: A Commentary on D'Amico et al.'s Family Study
Tác giả: Lien-Chung Wei, Hsien-Jane Chiu
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  671.373
 
A Pilot Study to Assess the Impact of a Multifactorial Explanation for Mental Illness on Prejudicial Attitudes Towards P...
Tác giả: Hailey A Segall, Amber M Aeilts, Dawn C Allain, Jehannine C Austin, Danielle M Dick, Abigail B Shoben
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  146.7
 
New Insights Into TRMT10A Syndrome: Case Report and Literature Review
Tác giả: Graziana Ceraolo, Ambra Butera, Francesco Calì, Gabriella Di Rosa, Antonino Musumeci, Antonio Gennaro Nicotera, Maria Spanò, Giulia Spoto, Mirella Vinci, Girolamo Aurelio Vitello
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  496.3374
 
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach
Tác giả: Ewan Carr, Katherine J Aitchison, Anne Farmer, Neven Henigsberg, Raquel Iniesta, Wolfgang Maier, Peter McGuffin, Ole Mors, Marcella Rietschel, Rudolf Uher
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  553.3
 
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distal
Tác giả: I Claus, B T Baune, A Buness, F Degenhardt, A J Forstner, I Giegling, A M Hartmann, U Heilbronner, S Heilmann-Heimbach, A Heimbach, L Henschel, P Hoffmann, J Kammerer-Ciernioch, D Klein, A C Koller, B Konte, K U Ludwig, A Maaser-Hecker, C M Mathey, I Nenadić, M M Nöthen, A Philipsen, M Rietschel, D Rujescu, B Schmidt, T G Schulze, L Sindermann, S Sivalingam, F Streit, T Stürmer, H Vedder, M Wagner, A Weiß
Xuất bản: United States: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2025
Bộ sưu tập: NCBI
ddc:  553.3
 
Maize transcription factor ZmEREB167 negatively regulates starch accumulation and kernel size
Tác giả: Xiangyu Qing, Jianrui Li, Haiming Zhao, Zhijia Yang, Zhen Lin, Wei Wang, Fei Yi, Jian Chen, Qiujie Liu, Weibin Song, Jinsheng Lai, Baojian Chen
Xuất bản: China: Journal of genetics and genomics = Yi chuan xue bao , 2025
Bộ sưu tập: NCBI
ddc:  289.333
 
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia
Tác giả: Qiao Wei, Wenlu Fan, Wanzhong Ge, Zhi-Ying Wu, Hong-Fu Li, Pei-Shan Wang, Man Xu, Hai-Lin Dong, Hao Yu, Jialan Lyu, Wen-Jiao Luo, Dian-Fu Chen
Xuất bản: China: Journal of genetics and genomics = Yi chuan xue bao , 2025
Bộ sưu tập: NCBI
ddc:  636.0885
 

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