Exome

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March 2017

http://publications.mcgill.ca/humangenetics/2017/03/16/jan-19-17/

Human Genetics Newsletter 03/16/2017

04-october-13
Comparison of global gene expression profiles of microdissected human foetal Leydig cells with their normal and hyperplastic adult equivalents.

https://www.ncbi.nlm.nih.gov/pubmed/28333300?dopt=Abstract

pubmed: wnt1 03/24/2017

mol hum reprod
2017-18: HGSS Call for Nominations

http://publications.mcgill.ca/humangenetics/2017/05/24/friendly-reminder/

Human Genetics Newsletter 05/24/2017
June 2017

http://publications.mcgill.ca/humangenetics/2017/05/24/jan-19-17/

Human Genetics Newsletter 05/24/2017
Funding, Jobs and Other Announcements:

http://publications.mcgill.ca/humangenetics/2017/05/08/funding-jobs-and-other-announcements-3/

Human Genetics Newsletter 05/08/2017
Simon Papillon-Cavanagh announced April month winner of Étudiants-chercheurs étoiles award

http://publications.mcgill.ca/humangenetics/2017/04/13/in-memory-of-bartha-knoppers-boon/

Human Genetics Newsletter 04/13/2017
Modulatory Effects of Guarana (Paullinia cupana) on Adipogenesis.

https://www.ncbi.nlm.nih.gov/pubmed/28632199?dopt=Abstract

pubmed: wnt1
Methyltransferase G9A Regulates Osteogenesis via Twist Gene Repression.

https://www.ncbi.nlm.nih.gov/pubmed/28644763?dopt=Abstract

pubmed: wnt1
Epigenetically controlled Six3 expression regulates glioblastoma cell proliferation and invasion alongside modulating the activation levels of WNT pathway members.

https://www.ncbi.nlm.nih.gov/pubmed/28643150?dopt=Abstract

pubmed: wnt1
The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling.

https://www.ncbi.nlm.nih.gov/pubmed/28041905?dopt=Abstract

pubmed: wnt1
Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility.

https://www.ncbi.nlm.nih.gov/pubmed/28646443?dopt=Abstract

pubmed: wnt1
The loss of Krüppel-like factor 15 in Foxd1(+) stromal cells exacerbates kidney fibrosis.

https://www.ncbi.nlm.nih.gov/pubmed/28651950?dopt=Abstract

pubmed: wnt1
Small Interfering RNA Targeting Dickkopf-1 Contributes to Neuroprotection After Intracerebral Hemorrhage in Rats.

https://www.ncbi.nlm.nih.gov/pubmed/28097491?dopt=Abstract

pubmed: wnt1
Analysis of the Function of Apoptosis during Imaginal Wing Disc Regeneration in Drosophila melanogaster.

https://www.ncbi.nlm.nih.gov/pubmed/27893747?dopt=Abstract

pubmed: wnt1
Human mutations in integrator complex subunits link transcriptome integrity to brain development.

https://www.ncbi.nlm.nih.gov/pubmed/28542170?dopt=Abstract

pubmed: wnt1
Strengthening brittle bones.

https://www.ncbi.nlm.nih.gov/pubmed/28659442?dopt=Abstract

pubmed: wnt1
Exome sequencing revealed a novel homozygous splice site variant in WNT1 gene underlying osteogenesis imperfecta type 3.

https://www.ncbi.nlm.nih.gov/pubmed/28665926?dopt=Abstract

pubmed: wnt1
Smooth Muscle Cells Derived From Second Heart Field and Cardiac Neural Crest Reside in Spatially Distinct Domains in the Media of the Ascending Aorta.

https://www.ncbi.nlm.nih.gov/pubmed/28663257?dopt=Abstract

pubmed: wnt1
Serum levels of WNT1-inducible signaling pathway protein-1 (WISP-1): a noninvasive biomarker of renal fibrosis in subjects with chronic kidney disease.

https://www.ncbi.nlm.nih.gov/pubmed/28670380?dopt=Abstract

pubmed: wnt1
Abnormality of Klotho Signaling Is Involved in Polycystic Ovary Syndrome.

https://www.ncbi.nlm.nih.gov/pubmed/28673204?dopt=Abstract

pubmed: wnt1
Drosophila DDX3/Belle Exerts Its Function Outside of the Wnt/Wingless Signaling Pathway.

https://www.ncbi.nlm.nih.gov/pubmed/28030561?dopt=Abstract

pubmed: wnt1
Drosophila Wnt and STAT Define Apoptosis-Resistant Epithelial Cells for Tissue Regeneration after Irradiation.

https://www.ncbi.nlm.nih.gov/pubmed/27584613?dopt=Abstract

pubmed: wnt1
Adult Muscle Formation Requires Drosophila Moleskin for Proliferation of Wing Disc-Associated Muscle Precursors.

https://www.ncbi.nlm.nih.gov/pubmed/28249984?dopt=Abstract

pubmed: wnt1
CRISPR/Cas9-Mediated Zebrafish Knock-in as a Novel Strategy to Study Midbrain-Hindbrain Boundary Development.

https://www.ncbi.nlm.nih.gov/pubmed/28713249?dopt=Abstract

pubmed: wnt1
Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.

https://www.ncbi.nlm.nih.gov/pubmed/28725987?dopt=Abstract

pubmed: wnt1

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