Literature DB >> 27584555

Histomorphological Phenotyping of the Adult Mouse Brain.

Anna Mikhaleva1, Meghna Kannan1,2,3,4,5, Christel Wagner2,3,4,5, Binnaz Yalcin1,2,3,4,5.   

Abstract

This article describes a series of standard operating procedures for morphological phenotyping of the mouse brain using basic histology. Many histological studies of the mouse brain use qualitative approaches based on what the human eye can detect. Consequently, some phenotypic information may be missed. Here we describe a quantitative approach for the assessment of brain morphology that is simple and robust. A total of 78 measurements are made throughout the brain at specific and well-defined regions, including the cortex, the hippocampus, and the cerebellum. Experimental design and timeline considerations, including strain background effects, the importance of sectioning quality, measurement variability, and efforts to correct human errors are discussed. © 2016 by John Wiley & Sons, Inc.
Copyright © 2016 John Wiley & Sons, Inc.

Entities:  

Keywords:  brain morphology; histology; mouse; phenotyping

Mesh:

Year:  2016        PMID: 27584555     DOI: 10.1002/cpmo.12

Source DB:  PubMed          Journal:  Curr Protoc Mouse Biol        ISSN: 2161-2617


  10 in total

1.  Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.

Authors:  Anna R Duncan; Antonio Vitobello; Stephan C Collins; Valerie E Vancollie; Christopher J Lelliott; Lance Rodan; Jiahai Shi; Ann R Seman; Emanuele Agolini; Antonio Novelli; Paolo Prontera; Maria J Guillen Sacoto; Teresa Santiago-Sim; Aurélien Trimouille; Cyril Goizet; Mathilde Nizon; Ange-Line Bruel; Christophe Philippe; Patricia E Grant; Monica H Wojcik; Joan Stoler; Casie A Genetti; Marieke F van Dooren; Saskia M Maas; Marielle Alders; Laurence Faivre; Arthur Sorlin; Grace Yoon; Binnaz Yalcin; Pankaj B Agrawal
Journal:  Am J Hum Genet       Date:  2020-11-23       Impact factor: 11.025

2.  Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.

Authors:  Norine Voisin; Rhonda E Schnur; Sofia Douzgou; Susan M Hiatt; Cecilie F Rustad; Natasha J Brown; Dawn L Earl; Boris Keren; Olga Levchenko; Sinje Geuer; Sarah Verheyen; Diana Johnson; Yuri A Zarate; Miroslava Hančárová; David J Amor; E Martina Bebin; Jasmin Blatterer; Alfredo Brusco; Gerarda Cappuccio; Joel Charrow; Nicolas Chatron; Gregory M Cooper; Thomas Courtin; Elena Dadali; Julien Delafontaine; Ennio Del Giudice; Martine Doco; Ganka Douglas; Astrid Eisenkölbl; Tara Funari; Giuliana Giannuzzi; Ursula Gruber-Sedlmayr; Nicolas Guex; Delphine Heron; Øystein L Holla; Anna C E Hurst; Jane Juusola; David Kronn; Alexander Lavrov; Crystle Lee; Séverine Lorrain; Else Merckoll; Anna Mikhaleva; Jennifer Norman; Sylvain Pradervand; Darina Prchalová; Lindsay Rhodes; Victoria R Sanders; Zdeněk Sedláček; Heidelis A Seebacher; Elizabeth A Sellars; Fabio Sirchia; Toshiki Takenouchi; Akemi J Tanaka; Heidi Taska-Tench; Elin Tønne; Kristian Tveten; Giuseppina Vitiello; Markéta Vlčková; Tomoko Uehara; Caroline Nava; Binnaz Yalcin; Kenjiro Kosaki; Dian Donnai; Stefan Mundlos; Nicola Brunetti-Pierri; Wendy K Chung; Alexandre Reymond
Journal:  Am J Hum Genet       Date:  2021-05-06       Impact factor: 11.025

3.  WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy.

Authors:  Meghna Kannan; Efil Bayam; Christel Wagner; Bruno Rinaldi; Perrine F Kretz; Peggy Tilly; Marna Roos; Lara McGillewie; Séverine Bär; Shilpi Minocha; Claire Chevalier; Chrystelle Po; Jamel Chelly; Jean-Louis Mandel; Renato Borgatti; Amélie Piton; Craig Kinnear; Ben Loos; David J Adams; Yann Hérault; Stephan C Collins; Sylvie Friant; Juliette D Godin; Binnaz Yalcin
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-12       Impact factor: 11.205

4.  The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.

Authors:  Maria Nicla Loviglio; Thomas Arbogast; Aia Elise Jønch; Stephan C Collins; Konstantin Popadin; Camille S Bonnet; Giuliana Giannuzzi; Anne M Maillard; Sébastien Jacquemont; Binnaz Yalcin; Nicholas Katsanis; Christelle Golzio; Alexandre Reymond
Journal:  Am J Hum Genet       Date:  2017-09-28       Impact factor: 11.025

5.  Aortic Cross-Clamping to Provide Differential Fixation by Perfusion.

Authors:  Mackenzie M Moore; Emilyn U Alejandro
Journal:  Curr Protoc       Date:  2021-03

6.  A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice.

Authors:  Michał Szpak; Stephan C Collins; Yan Li; Xiao Liu; Qasim Ayub; Marie-Christine Fischer; Valerie E Vancollie; Christopher J Lelliott; Yali Xue; Binnaz Yalcin; Huanming Yang; Chris Tyler-Smith
Journal:  Mol Biol Evol       Date:  2021-12-09       Impact factor: 16.240

7.  Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.

Authors:  Lettie E Rawlins; Hashem Almousa; Shazia Khan; Stephan C Collins; Miroslav P Milev; Joseph Leslie; Djenann Saint-Dic; Valeed Khan; Ana Maria Hincapie; Jacob O Day; Lucy McGavin; Christine Rowley; Gaurav V Harlalka; Valerie E Vancollie; Wasim Ahmad; Christopher J Lelliott; Asma Gul; Binnaz Yalcin; Andrew H Crosby; Michael Sacher; Emma L Baple
Journal:  PLoS Genet       Date:  2022-03-17       Impact factor: 5.917

8.  Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.

Authors:  Stephan C Collins; Valerie E Vancollie; Anna Mikhaleva; Christel Wagner; Rebecca Balz; Christopher J Lelliott; Binnaz Yalcin
Journal:  Int J Mol Sci       Date:  2022-09-29       Impact factor: 6.208

9.  Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis.

Authors:  Stephan C Collins; Anna Mikhaleva; Katarina Vrcelj; Valerie E Vancollie; Christel Wagner; Nestor Demeure; Helen Whitley; Meghna Kannan; Rebecca Balz; Lauren F E Anthony; Andrew Edwards; Hervé Moine; Jacqueline K White; David J Adams; Alexandre Reymond; Christopher J Lelliott; Caleb Webber; Binnaz Yalcin
Journal:  Nat Commun       Date:  2019-08-01       Impact factor: 14.919

10.  Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.

Authors:  Véronique Brault; Thu Lan Nguyen; Javier Flores-Gutiérrez; Giovanni Iacono; Marie-Christine Birling; Valérie Lalanne; Hamid Meziane; Antigoni Manousopoulou; Guillaume Pavlovic; Loïc Lindner; Mohammed Selloum; Tania Sorg; Eugene Yu; Spiros D Garbis; Yann Hérault
Journal:  PLoS Genet       Date:  2021-09-29       Impact factor: 5.917

  10 in total

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