Results 111 to 120 of about 329,928 (259)

Living with Risk, Aging with Uncertainty: A Narrative Review of Health and Genetic Vulnerability in Huntington’s Disease

Biomedicines
Background/Objectives: Huntington’s disease (HD) is an autosomal dominant, neurodegenerative disorder that, because of the availability of presymptomatic genetic testing, places at-risk individuals in an anticipatory situation of great emotional, ethical,
Adriana V. Muñoz-Ortega, David Conde Caballero, Lorenzo Mariano Juárez   +2 more
doaj   +1 more source

Aspectos genéticos do transtorno obsessivo-compulsivo

Brazilian Journal of Psychiatry, 2001
Since the first descriptions of obsessive-compulsive disorder (OCD), genetic factors have been implicated in the etiology of the illness. Twin studies show a high concordance rate for monozygotic twins.
Gonzalez Christina H
doaj  

Evolutionary biology and anthropology suggest biome reconstitution as a necessary approach toward dealing with immune disorders [PDF]

, 2013
Industrialized society currently faces a wide range of non-infectious, immune-related pandemics. These pandemics include a variety of autoimmune, inflammatory and allergic diseases that are often associated with common environmental triggers and with ...
Adler, Allen, Arbes, Backhed, Bagnasco, Bartlett, Becker, Becker, Bethell, Bickler, Bilbo, Bilbo, Black, Borkow, Brenner, Bronstein, Brown, Cannell, Capron, Casanova, Chandra, Correale, Correale, Dantzer, Davis, Day, de Borst, Devalapalli, Dominguez-Bello, Elliott, Fairweather, Fan, Fanaro, Fava, Feary, Feary, Feazel, Floch, Floch, Foliaki, Fumagalli, Gale, Gangoso, Gao, Genuis, Gernsbacher, Glaser, Gouin, Green, Grice, Guaraldi, Guarner, Guo, Hadley, Hanski, Hansson, Hare, Heck, Herre, Hewitson, Holick, Hummelen, Ippoliti, ISAAC Steering Committee, Isack, Jane Costello, Karst, Kelly, Kendall-Tackett, Khoruts, Kiecolt-Glaser, Kong, Krishnadas, Kronman, Lakhan, Leboyer, Lee, Lesher, Lin, Liu, Liu, Lowry, Lucas, Mackie, Malcolm, Mark, Mehta, Merrett, Meyer, Mills, Moylan, Nickens, Northrop-Clewes, Ollerton, Ollerton, Parker, Reiche, Rook, Rook, Rook, Rook, Rook, Ryder, Saha, Salim, Saunders, Sharief, Singh, Smith, Stojanovich, Strachan, Sullivan, Summers, Summers, Surawicz, Tilp, Trama, Turton, U.S. Food and Drug Administration, Valasquez-Manoff, van Nood, Vehik, von Hertzen, Waeber, Wang, Warren, Wilson, Wilson, Wohlleben, Wold, Yazdanbakhsh, Yoshioka, Zandman-Goddard, Zhou   +133 more
core   +1 more source

Genetic predisposition to Behcet's disease mediated by a IL10RA enhancer polymorphism

Heliyon
Background: Several studies suggested the genetic association between IL10RA variants and susceptibility to Behcet's disease (BD). However, the precise mechanism of the association is still unknown.
Handan Tan, Zhenyu Zhong, Xiaojie Feng, Xiang Luo, Qingfeng Cao, Peizeng Yang   +5 more
doaj   +1 more source

Frailty, genetic predisposition, and incident chronic kidney disease

Scientific Reports
Frailty is common among individuals with chronic kidney disease (CKD), whereas its impact on incident CKD risk remains unknown. This study aimed to prospectively evaluate the association between frailty and incident CKD risk, exploring the potential modification role of genetic risk factors (GRS).
Shanshan Zou, Ying Sun, Yinuo Zhou, Bowei Yu, Jiang Li, Yuefeng Yu, Jianing Chen, Yujie Li, Ningjian Wang, Li Wang   +9 more
openaire   +3 more sources

Genetically selected baby free of inherited predisposition to early-onset Alzheimer's disease [PDF]

, 2002
Merle Spriggs
openalex   +1 more source

Genetics and Epigenetics of Arrhythmia and Heart Failure

Frontiers in Genetics, 2013
Heart failure (HF) is the end stage of several pathological cardiac conditions including myocardial infarction, cardiac hypertrophy and hypertension. Various molecular and cellular mechanisms are involved in the development of HF. At the molecular level,
Burcu eDuygu, Ella M. Poels, Paula A. Da Costa Martins   +2 more
doaj   +1 more source

Association between SNCA Intron and genetic predisposition to sporadic Parkinson's disease: a meta-analysis based on 49576 individuals [PDF]

, 2021
Peng Li, Zuqiang Fu, Lei Yan, Mingyang Du, Wei-guoLiu   +4 more
openalex   +1 more source

Genetic Bases for Predisposition to Common Multifactorial Disease in Man. Part II [PDF]

, 2007
Rumena Petkova, Stoyan Chakarov, Varban Ganev   +2 more
openalex   +1 more source

Genetic variability shapes the alternative pathway complement activity and predisposition to complement‐related diseases [PDF]

, 2022
Santiago Rodrı́guez de Córdoba
openalex   +1 more source