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31-40 trong số 42 kết quả
A systems biology, whole-genome association analysis of the molecular regulation of biomass growth and composition in Po...
Tác giả:
Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2014
Bộ sưu tập: Báo, Tạp chí
ddc:  628.5
 
Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working Group
Tác giả: Guillaume Cogan, Marie-Bérengère Troadec, Pascale Saugier-Veber, Françoise Devillard, Marie-Hélène Saint-Frison, David Geneviève, François Vialard, Emmanuelle Rial-Sebbag, Delphine Héron, Tania Attie-Bitach, Alexandra Benachi
Xuất bản: England: Prenatal diagnosis , 2025
Bộ sưu tập: NCBI
ddc:  370.119
 
Analysis of whole-exome data of nonobese NAFLD patients from India reveals association with new markers on functionally relevant genes and pathways
Tác giả: Arnab Ghosh, Anamita Barik, Abhijit Chowdhury, Parha P Majumder, Rajesh K Rai, Jeffrey D Wall
Xuất bản: India: Journal of genetics , 2025
Bộ sưu tập: NCBI
ddc:  633.14
 
Whole exome sequencing diagnosing syndromic and non-syndromic hearing loss with expansion of the phenotypic spectrum related to TMC1 variants
Tác giả: Nagham M Elbagoury, Engy A Ashaat, Anas M Askoura, Mona L Essawi, Mona K Mekkawy, Peter M Milad, Ragaey Y Mohamed
Xuất bản: Germany: European journal of pediatrics , 2025
Bộ sưu tập: NCBI
ddc:  794.147
 
Exome-wide association analysis identifies novel risk loci for alcohol-associated hepatitis
Tác giả: Qiaoping Yuan, Colin Hodgkinson, David Goldman, Xiaochen Liu, Bruce Barton, Nancy Diazgranados, Melanie Schwandt, Timothy Morgan, Ramon Bataller, Suthat Liangpunsakul, Laura E Nagy
Xuất bản: United States: Hepatology (Baltimore, Md , 2025
Bộ sưu tập: NCBI
ddc:  304.663
 
Whole exome sequencing uncovers rare variants associated with PCOS susceptibility in Indian women
Tác giả: Medini Samant, Mahalakshmi Bhat, Roshan Dadachanji, Digumarthi V S Sudhakar, Anushree Patil, Srabani Mukherjee
Xuất bản: England: Systems biology in reproductive medicine , 2025
Bộ sưu tập: NCBI
ddc:  523.015
 
Clinical Exome Sequencing Identifies, Two Homozygous LOXHD1 Variants in Two Inbred Families With Pre-Lingual Hearing Loss From South India
Tác giả: Mathuravalli Krishnamoorthy, Chandru Jayasankaran, Sorna Lakshmi, Chodisetty Sarvani, Jeffrey Justin Margret, Subathra Mahalingam, Pavithra Amritkumar, Paridhy Vanniya Subramanyam, Sarrath Rathnaraajan S, C R Srikumari Srisailapathy
Xuất bản: England: Annals of human genetics , 2025
Bộ sưu tập: NCBI
ddc:  346.038
 
Exome sequencing shows same pattern of clonal tumor mutational burden, intratumor heterogenicity and clonal neoantigen between autologous tumor and Vigil product
Tác giả: David Willoughby, Ernest Bognar, John Nemunaitis, Laura Stanbery, Casey Nagel, Gladice Wallraven, Aman Pruthi, Nicholas Bild, Ericca Stamper, Donald Rao, Adam Walter
Xuất bản: England: Scientific reports , 2025
Bộ sưu tập: NCBI
ddc:  551.566
 
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects
Tác giả: Gloria K E Zodanu, John H Hwang, Ucla Congenital Heart Defects-BioCore Faculty, Wayne W Grody, Gary M Satou, Glen S Van Arsdell, Stanly F Nelson, Marlin Touma, Jordan Mudery, Carlos Sisniega, Xuedong Kang, Lee-Kai Wang, Alexander Barsegian, Reshma M Biniwale, Ming-Sing Si, Nancy J Halnon
Xuất bản: Switzerland: International journal of molecular sciences , 2025
Bộ sưu tập: NCBI
ddc:  171.7
 
Genome-wide association study reveals putative regulators of bioenergy traits in <i>Populus deltoides</i> [e...
Tác giả:
Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2016
Bộ sưu tập: Báo, Tạp chí
ddc:  668.5
 

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