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Genetic Predisposition to Disease (Latest Articles)
Latest indexed articles for 'Genetic Predisposition to Disease'
Articles 1 to 10 of 200:
Genetic complexity of absence seizures in substrains of C3H mice.
15 Dec 2009 
Absence epilepsy is a common form of idiopathic generalized epilepsy whose etiology is poorly understood because of genetic and phenotypic heterogeneity. The inbred mouse strain C3H/He exhibits spontaneous absence seizures characterized by spike and ...
rec_pub_19170754-genetic-complexity-absence-seizures-substrains-c3h-mice.htm
13 Dec 2009 BACKGROUND: Our original studies reported an association between the iron-metabolism gene HFE and risk of childhood acute lymphoblastic leukemia (ALL), and a birth weight association in ALL. Through its effect on cell proliferation, iron is involved ...
rec_pub_19711434-hereditary-hemochromatosis-gene-hfe-variants-associated-birth-weight.htm
Mice mutant for genes associated with schizophrenia: common phenotype or distinct endophenotypes?
5 Dec 2009 Schizophrenia is a complex neuropsychiatric disorder whose etiology involves a mixture of genetic and environmental factors. By virtue of this complexity, schizophrenia is a field of research in which a number of key technologies converge: in ...
rec_pub_19728400-mice-mutant-genes-associated-schizophrenia-common-phenotype-distinct.htm
Fanconi anemia and biallelic BRCA2 mutation diagnosed in a young child with an embryonal CNS tumor.
29 Nov 2009 Medulloblastoma, the most common pediatric malignant brain tumor often arises sporadically; however, in a subgroup of patients, there exist familial conditions such as Fanconi anemia with biallelic BRCA2 mutation that predispose patients to ...
rec_pub_19530235-fanconi-anemia-biallelic-brca2-mutation-diagnosed-young-child.htm
The heritability and genetics of frontotemporal lobar degeneration.
Nov 2009 BACKGROUND: Frontotemporal lobar degeneration (FTLD) is a genetically and pathologically heterogeneous neurodegenerative disorder. METHODS: We collected blood samples from a cohort of 225 patients with a diagnosis within the FTLD spectrum and ...
rec_pub_19884572-the-heritability-genetics-frontotemporal-lobar-degeneration.htm
Two distinct subtypes of right temporal variant frontotemporal dementia.
Nov 2009 BACKGROUND: Right temporal frontotemporal dementia (FTD) is an anatomic variant of FTD associated with relatively distinct behavioral and cognitive symptoms. We aimed to determine whether right temporal FTD is a homogeneous clinical, imaging, and ...
rec_pub_19884571-two-distinct-subtypes-right-temporal-variant-frontotemporal-dementia.htm
30 Oct 2009 Inflammation is involved in the development of atherosclerosis. The CC chemokine receptor 5 (CCR5) initiates chemotaxis and modulates the inflammation secondary to atherosclerosis and related vascular diseases. The CCR5 Delta32 polymorphism ...
rec_pub_19874552-common-ccr-5-polymorphism-stroke-ccr-5-delta32-polymorphism.htm
30 Oct 2009 Particular alleles of the interleukin-1B (IL-1B) gene have been correlated with increased risk of atrophic gastritis and gastric cancer in the populations of East Asia and Europe. No such data exist from Peru, a developing country with a population ...
rec_pub_19861615-interleukin-1-beta-single-nucleotide-polymorphism-s-c-allele.htm
Association of IL2RA and IL2RB with rheumatoid arthritis: a replication study in a Dutch population.
30 Oct 2009 
rec_pub_19822714-association-il2ra-il2rb-rheumatoid-arthritis-replication-study-dutch.htm
Sarcoidosis: epidemiology, etiology, pathogenesis, and genetics.
30 Oct 2009
rec_pub_19857640-sarcoidosis-epidemiology-etiology-pathogenesis-genetics.htm
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