相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
Pavlo L. Kovalenko et al.
BMC GENOMICS (2010)
Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: A systems biology based approach
Alexandra C. Silveira et al.
VISION RESEARCH (2010)
Gene Expression Changes in Areas of Focal Loss of Retinal Ganglion Cells in the Retina of DBA/2J Mice
Lampros Panagis et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
MicroRNA Profile of the Developing Mouse Retina
Laszlo Hackler et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction
Neena B. Haider et al.
EXPERIMENTAL EYE RESEARCH (2009)
A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa
Anneke I. den Hollander et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene
Manfred Kayser et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisis
Britt A. Johnson et al.
GENETICS (2008)
Effect of genetic background on acoustic startle response in fragile X knockout mice
Vanessa Errijgers et al.
GENETICS RESEARCH (2008)
Loss of RB1 induces non-proliferative retinoma:: increasing genomic instability correlates with progression to retinoblastoma
Helen Dimaras et al.
HUMAN MOLECULAR GENETICS (2008)
Mapping of genetic modifiers of Eya1bor/bor in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness
Haoru Niu et al.
MAMMALIAN GENOME (2008)
Mapping of genetic modifiers of Nr2e3rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity
Neena B. Haider et al.
MAMMALIAN GENOME (2008)
Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA
Lars G. Fritsche et al.
NATURE GENETICS (2008)
Medical progress: Age-related macular degeneration
Rama D. Jager et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Genetic modifiers of retinal degeneration in the rd3 mouse
Michael Danciger et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2008)
Coding and noncoding variants in the CFH gene and cigarette smoking influence the risk of age-related macular degeneration in a Japanese population
Keisuke Mori et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2007)
A typology of photoreceptor gene expression patterns in the mouse
Joseph C. Corbo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
The polymorphism architecture of mouse genetic resources elucidated using genome-wide resequencing data: implications for QTL discovery and systems genetics
Adam Roberts et al.
MAMMALIAN GENOME (2007)
Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations
Karen L. Svenson et al.
JOURNAL OF APPLIED PHYSIOLOGY (2007)
Mouse inbred strain differences in ethanol drinking to intoxication
J. S. Rhodes et al.
GENES BRAIN AND BEHAVIOR (2007)
Identification and characterization of MicroRNAs expressed in the mouse eye
Marianthi Karali et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2007)
A high-resolution map of segmental DNA copy number variation in the mouse genome
Timothy A. Graubert et al.
PLOS GENETICS (2007)
Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects
Alessandro Iannaccone et al.
VISION RESEARCH (2006)
The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation
Neena B. Haider et al.
VISUAL NEUROSCIENCE (2006)
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration
Julian Maller et al.
NATURE GENETICS (2006)
Visual detection, pattern discrimination and visual acuity in 14 strains of mice
A. A. Wong et al.
GENES BRAIN AND BEHAVIOR (2006)
The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear
Amy E. Kiernan et al.
PLOS GENETICS (2006)
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk
A Rivera et al.
HUMAN MOLECULAR GENETICS (2005)
Susceptibility genes for age-related maculopathy on chromosome 10q26
J Jakobsdottir et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Notch signaling, brain development, and human disease
JL Lasky et al.
PEDIATRIC RESEARCH (2005)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Complement factor H polymorphism and age-related macular degeneration
AO Edwards et al.
SCIENCE (2005)
Complement factor H variant increases the risk of age-related macular degeneration
JL Haines et al.
SCIENCE (2005)
Interstitial lung disease in children - genetic background and associated phenotypes
D Hartl et al.
RESPIRATORY RESEARCH (2005)
A comparison of ERG abnormalities in XLRS and XLCSNB
K Bradshaw et al.
DOCUMENTA OPHTHALMOLOGICA (2004)
Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration
SK Iyengar et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation
KM Nishiguchi et al.
NATURE (2004)
Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy
A Hameed et al.
JOURNAL OF MEDICAL GENETICS (2003)
Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/+ tf/tf has severely reduced hippocampal commissure and absent corpus callosum
D Wahlsten et al.
BRAIN RESEARCH (2003)
Analysis of gene expression in the developing mouse retina
E Díaz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Regulation of ganglion cell production by notch signaling during retinal development
AO Silva et al.
JOURNAL OF NEUROBIOLOGY (2003)
Six3 and Six6 activity is modulated by members of the groucho family
J Lopez-Rios et al.
DEVELOPMENT (2003)
Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration
RH Guymer et al.
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2002)
VSX1:: A gene for posterior polymorphous dystrophy and keratoconus
E Héon et al.
HUMAN MOLECULAR GENETICS (2002)
Haploinsufficiency of NSD1 causes Sotos syndrome
N Kurotaki et al.
NATURE GENETICS (2002)
Genetic modification of retinal degeneration in tubby mice
A Ikeda et al.
EXPERIMENTAL EYE RESEARCH (2002)
Pathfinding and error correction by retinal axons:: The role of astray/robo2
LD Hutson et al.
NEURON (2002)
Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice
NB Haider et al.
HUMAN MOLECULAR GENETICS (2001)
Electroconvulsive thresholds of inbred mouse strains
WN Frankel et al.
GENOMICS (2001)
The murine cone photoreceptor: A single cone type expresses both S and M opsins with retinal spatial patterning
ML Applebury et al.
NEURON (2000)
Further evidence for an association of ABCR alleles with age-related macular degeneration
R Allikmets
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1
CK Chen et al.
NATURE (2000)
分享论文
