Golgi-Cox staining step by step

by Sami eZaqout, Sami eZaqout, Angela M Kaindl, Angela M Kaindl
Published 2016-03-01

Immunofluorescence Staining of Paraffin Sections Step by Step

by Sami Zaqout, Lena-Luise Becker, Lena-Luise Becker, Lena-Luise Becker, Angela M. Kaindl, Angela M. Kaindl, Angela M. Kaindl
Published 2020-11-01

Maintenance of Elective Patient Care at Berlin University Children's Hospital During the COVID-19 Pandemic

by Nicolas Terliesner, Alexander Rosen, Angela M. Kaindl, Angela M. Kaindl, Angela M. Kaindl, Uwe Reuter, Kai Lippold, Marcus A. Mall, Marcus A. Mall, Marcus A. Mall, Horst von Bernuth, Horst von Bernuth, Horst von Bernuth, Horst von Bernuth, Alexander Gratopp
Published 2021-08-01

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development

by Sami Zaqout, Paraskevi Bessa, Nadine Krämer, Gisela Stoltenburg-Didinger, Angela M. Kaindl
Published 2017-02-01

Novel Alternative Splice Variants of Mouse Cdk5rap2.

by Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, Ethiraj Ravindran, Shyamala Mani, Olaf Ninnemann, Angela M Kaindl
Published 2015-01-01

Altered inhibition and excitation in neocortical circuits in congenital microcephaly

by Sami Zaqout, Kathrin Blaesius, Yuan-Ju Wu, Stefanie Ott, Nadine Kraemer, Lena-Luise Becker, Marta Rosário, Christian Rosenmund, Ulf Strauss, Angela M. Kaindl
Published 2019-09-01

The somatostatin 2A receptor is enriched in migrating neurons during rat and human brain development and stimulates migration and axonal outgrowth.

by Virginia Le Verche, Angela M Kaindl, Catherine Verney, Zsolt Csaba, Stéphane Peineau, Paul Olivier, Homa Adle-Biassette, Christophe Leterrier, Tania Vitalis, Julie Renaud, Bénédicte Dargent, Pierre Gressens, Pascal Dournaud
Published 2009-01-01

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.

by Tao Chen, Bin Zhang, Thomas Ziegenhals, Archana B Prusty, Sebastian Fröhler, Clemens Grimm, Yuhui Hu, Bernhard Schaefke, Liang Fang, Min Zhang, Nadine Kraemer, Angela M Kaindl, Utz Fischer, Wei Chen
Published 2019-10-01

Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation

by Bianca Hartmann, Timothy Wai, Hao Hu, Thomas MacVicar, Luciana Musante, Björn Fischer-Zirnsak, Werner Stenzel, Ralph Gräf, Lambert van den Heuvel, Hans-Hilger Ropers, Thomas F Wienker, Christoph Hübner, Thomas Langer, Angela M Kaindl
Published 2016-08-01

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

by Ethiraj Ravindran, Hao Hu, Scott A Yuzwa, Luis R Hernandez-Miranda, Nadine Kraemer, Olaf Ninnemann, Luciana Musante, Eugen Boltshauser, Detlev Schindler, Angela Hübner, Hans-Christian Reinecker, Hans-Hilger Ropers, Carmen Birchmeier, Freda D Miller, Thomas F Wienker, Christoph Hübner, Angela M Kaindl
Published 2017-04-01

Arhgef2 regulates neural differentiation in the cerebral cortex through mRNA m6A-methylation of Npdc1 and Cend1

by Pei Zhou, Yifei Qi, Xiang Fang, Miaomiao Yang, Shuxin Zheng, Caihua Liao, Fengying Qin, Lili Liu, Hong Li, Yan Li, Ethiraj Ravindran, Chuanbo Sun, Xinshu Wei, Wen Wang, Liang Fang, Dingding Han, Changgeng Peng, Wei Chen, Na Li, Angela M. Kaindl, Hao Hu
Published 2021-06-01