Results 131 to 140 of about 15,770 (195)

RS1 Gene [PDF]

, 2020
openaire   +1 more source

Bullous X linked retinoschisis: clinical features and prognosis [PDF]

, 2018
BACKGROUND/AIMS: A subset of patients with X linked retinoschisis (XLRS) have bullous schisis cavities in the peripheral retina. This study describes the characteristics and prognosis of the bullous form of XLRS.
Fahim, A, Hinds, A-M, Michaelides, M, Moore, AT, Wong, SC   +4 more
core  

Introduction of an RS1 mutation causative variant consistent with identified XLRS patient using CRISPR/Cas9 technology in normal iPSC

Stem Cell Research
X-linked retinoschisis (XLRS) is a common retinal genetic disease that occurs in juvenile males and causes progressive visual impairment. This presents a schisis in the macula or peripheral retina of bilateral eyes, which has no effective treatment. Here,
Xihao Sun, Shengru Mao, Yuqin Liang, Chunwen Duan, Zekai Cui, Jianing Gu, Bing Jiang, Chengcheng Ding, Jiansu Chen, Shibo Tang   +9 more
doaj   +1 more source

Mouse U2af1-rs1 is a neomorphic imprinted gene.

Mouse U2af1-rs1 is a neomorphic imprinted gene.
identifier:oai:t2r2.star.titech.ac.jp ...
openaire  

Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout.

Molecular vision, 2006
The pineal gland shares a common neuroectoderm origin with the retina, and like the retina, regulates circadian rhythms through melatonin secretion. Recent expressed tag sequence (EST) analysis showed that several gene mutations, including RS1, which cause retinal degeneration, are also expressed in the pineal gland.
Takada, Y., Fariss, R., Moller, M., Bush, R., Rushing, E., Sieving, P.   +5 more
openaire   +1 more source

Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis.

Molecular vision, 2007
X-linked juvenile retinoschisis (XLRS) is the leading cause of macular degeneration in males. This condition is caused by mutations in the RS1 gene and is, characterized by schisis within the retina. The purpose of this study was to identify the mutations in the RS1 gene associated with XLRS in an Indian cohort.The coding region of RS1 was analyzed for
Balasubbu, Suganthalakshmi, Dhananjay, Shukla, Anand, Rajendran, Ramasamy, Kim, Jeyabalan, Nallathambi, Periasamy, Sundaresan   +5 more
openaire   +1 more source

Indian Farmers' Valuation of Yield Distributions: Will poor farmers value 'pro-poor' seeds? [PDF]

Potential poverty traps among the rural poor suggest a need to reduce poor farmers?vulnerability by stabilizing crop yields and limiting yield losses.
Travis Lybbert
core  

Dark Rearing Does Not Alter Developmental Retinoschisis Cavity Formation in Rs1 Gene Knockout Rat Model of X-Linked Retinoschisis. [PDF]

Genes (Basel)
Smit-McBride Z, Cho IH, Sun N, Thomas S, Sieving PA.   +4 more
europepmc   +1 more source

A Novel mechanism for depot-specific leptin gene expression regulation and its persistence after weight loss. [PDF]

iScience
Taege N, Britsemmer JH, Israel A, Krause C, Junge S, Feuchtinger A, Ussar S, Pfluger PT, Gemoll T, Schriever SC, Kirchner H.   +10 more
europepmc   +1 more source

Laterally spreading AAV.SPR enables safe and efficient RS1 delivery to the macula after peripheral subretinal injection. [PDF]

Mol Ther
Andres-Mateos E, Kozlowski C, Zhang H, Fajardo D, Xu E, Enamorado IN, Calabro KR, Rayaprolu S, Havlik LP, Handy TE, Plummer CE, Stevenson V, Rind H, Leahy M, Boyd RF, Coleman KE, Boye SL, Boye SE.   +17 more
europepmc   +1 more source