(Q46277943)

21 December 2017

title

CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH). (English)

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21 December 2017

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Tingting Sui

1

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21 December 2017

Lin Yuan

2

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21 December 2017

Huan Liu

3

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21 December 2017

Mao Chen

4

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21 December 2017

Jichao Deng

5

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21 December 2017

Yong Wang

6

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21 December 2017

Zhanjun Li

7

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21 December 2017

Liangxue Lai

8

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21 December 2017

publication date

28 April 2016

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21 December 2017

published in

Human Molecular Genetics

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21 December 2017

volume

25

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21 December 2017

issue

13

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21 December 2017

page(s)

2661-2671

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21 December 2017

A clinician's guide to X-linked hypophosphatemia

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDW125

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

21 January 2018

1 reference

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A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

21 January 2018

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Generation of knockout rabbits using transcription activator-like effector nucleases

21 January 2018

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The transgenic rabbit as model for human diseases and as a source of biologically active recombinant proteins.

21 January 2018

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One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

21 January 2018

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One-step generation of knockout pigs by zygote injection of CRISPR/Cas system

21 January 2018

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Simultaneous generation and germline transmission of multiple gene mutations in rat using CRISPR-Cas systems.

21 January 2018

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Efficient genome editing in zebrafish using a CRISPR-Cas system

21 January 2018

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Efficient gene knockout in goats using CRISPR/Cas9 system

21 January 2018

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Generation of multi-gene knockout rabbits using the Cas9/gRNA system

21 January 2018

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Efficient Generation of Myostatin Knock-Out Sheep Using CRISPR/Cas9 Technology and Microinjection into Zygotes

21 January 2018

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Fibroblast growth factor 23 acts on the parathyroid to decrease parathyroid hormone secretion

21 January 2018

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Calcium and phosphorus balance in extremely low birthweight infants in the first six weeks of life

21 January 2018

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X-chromosome inactivation

21 January 2018

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A novel Phex mutation in a new mouse model of hypophosphatemic rickets

21 January 2018

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Overexpression of human PHEX under the human beta-actin promoter does not fully rescue the Hyp mouse phenotype.

21 January 2018

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Renal phosphate loss in hereditary and acquired disorders of bone mineralization.

21 January 2018

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The effects of bone marrow transplantation on X-linked hypophosphatemic mice.

21 January 2018

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Anti-FGF-23 neutralizing antibodies ameliorate muscle weakness and decreased spontaneous movement of Hyp mice

21 January 2018

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FGF-23 is a potent regulator of vitamin D metabolism and phosphate homeostasis

21 January 2018

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FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate

21 January 2018

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Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice

21 January 2018

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X-linked hypophosphataemia: a homologous disorder in humans and mice

21 January 2018

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Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets

21 January 2018

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Multiplex genome engineering using CRISPR/Cas systems

21 January 2018

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A rapid and general assay for monitoring endogenous gene modification

21 January 2018

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Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype

21 January 2018

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Adaptations of Goldner's Masson trichrome stain for the study of undecalcified plastic embedded bone

21 January 2018

1 reference

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Phenotype Presentation of Hypophosphatemic Rickets in Adults

21 January 2018

1 reference

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21 January 2018

Identifiers

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21 December 2017