نتایج جستجو برای: multigeneration

تعداد نتایج: 228  

Journal: :Genetics 2003
Mark C Ungerer C Randal Linder Loren H Rieseberg

The extent to which genetic background can influence allelic fitness is poorly understood, despite having important evolutionary consequences. Using experimental populations of Arabidopsis thaliana and map-based population genetic data, we examined a multigeneration response to selection in populations with differentiated genetic backgrounds. Replicated experimental populations of A. thaliana w...

Journal: :Clinical orthopaedics and related research 2010
George Feldman Chelsea Dalsey Kasia Fertala David Azimi Paolo Fortina Marcella Devoto Maurizio Pacifici Javad Parvizi

Developmental dysplasia of the hip (DDH) is a disabling condition that, depending on geography, can afflict between 20% and 80% of patients with end-stage arthritis of the hip. Despite its prevalence, the etiology of this disease remains unknown. DDH is a complex disorder with both environmental and genetic causes. Based on the literature the candidate genes for the disease are HOXB9, collagen ...

Journal: :Genetics 2008
Harri Vehviläinen Antti Kause Cheryl Quinton Heikki Koskinen Tuija Paananen

As a fitness trait, survival is assumed to exhibit low heritability due to strong selection eroding genetic variation and/or spatio-temporal variation in mortality agents reducing genetic and increasing residual variation. The latter phenomenon in particular may contribute to low heritability in multigeneration data, even if certain cohorts exhibit significant genetic variation. Analysis of sur...

Journal: :Ecology 2017
Mathew A Leibold Spencer R Hall Val H Smith David A Lytle

Diversity of primary producer is often surprisingly high, despite few limiting factors such as nutrients and light to facilitate species coexistence. In theory, the presence of herbivores could increase the diversity of primary producers, resolving this "paradox of the plankton." Little experimental evidence supports this natural enemies hypothesis, but previous tests suffer from several defici...

Journal: :Kidney international 2012
York Pei Zheng Lan Kairong Wang Miguel Garcia-Gonzalez Ning He Elizabeth Dicks Patrick Parfrey Gregory Germino Terry Watnick

Mutations of PKD1 and PKD2 account for most cases of autosomal dominant polycystic kidney disease (ADPKD). Compared with PKD2, patients with PKD1 typically have more severe renal disease. Here, we report a follow-up study of a unique multigeneration family with bilineal ADPKD (NFL10) in which a PKD1 disease haplotype and a PKD2 (L736X) mutation co-segregated with 18 and 14 affected individuals,...

Journal: :Journal of medical genetics 1992
H J Stern H M Saal J S Lee P R Fain D E Goldgar K N Rosenbaum D F Barker

Detailed clinical, ophthalmological, and molecular studies were performed on a multigeneration family in which there were many subjects with type 1 neurofibromatosis, a common autosomal dominant disorder. Affected family members displayed a wide range of clinical findings including, in two subjects, features seen in Noonan syndrome (triangular facies, downward slanting palpebral fissures, micro...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
E I Ginns P St Jean R A Philibert M Galdzicka P Damschroder-Williams B Thiel R T Long L J Ingraham H Dalwaldi M A Murray M Ehlert S Paul B G Remortel A P Patel M C Anderson C Shaio E Lau I Dymarskaia B M Martin B Stubblefield K M Falls J P Carulli T P Keith C S Fann L G Lacy C R Allen A M Hostetter R C Elston N J Schork J A Egeland S M Paul

Bipolar affective disorder (BPAD; manic-depressive illness) is characterized by episodes of mania and/or hypomania interspersed with periods of depression. Compelling evidence supports a significant genetic component in the susceptibility to develop BPAD. To date, however, linkage studies have attempted only to identify chromosomal loci that cause or increase the risk of developing BPAD. To det...

Journal: :The Journal of nutrition 2000
H C Chang M I Churchwell K B Delclos R R Newbold D R Doerge

Genistein, the principal soy isoflavone, was administered in the diet to male and female Sprague-Dawley rats as part of a multigeneration study of potential endocrine modulation. The rats were exposed to genistein in utero, through maternal milk, and as adults through postnatal d 140 via essentially isoflavone-free feed (approximately 0.5 microg/g) fortified at 5, 100 and 500 microg/g with geni...

Journal: :Genetics 1996
K E Zerba R E Ferrell C F Sing

We analyzed the age-dependence of the estimates of the parameters of the genetic architecture of plasma ApoE levels associated with ApoE gene variation. Our study sample included 1988 individuals in multigeneration pedigrees from the Rochester, MN, population. We used a 30-yr sliding window across the age range (5-90 yr) to estimate the age dependency of parameters. Additive ApoE allelic varian...

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