Lilian A. Carrera-Martinez

Bergisch Gladbach, NW, Germany

Last Updated: 09/26/2026

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Found 9 publications

A clinical-grade automated platform for the manufacturing of CAR-γδ T cells for immunotherapy.

A clinical-grade automated platform for the manufacturing of CAR-γδ T cells for immunotherapy.

Journal: Frontiers in immunology

Published: December 31, 2025

Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development.

Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development.

Journal: Human molecular genetics

Published: December 14, 2017

Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.

Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.

Journal: European journal of human genetics : EJHG

Published: February 02, 2017

Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement.

Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement.

Journal: Neurology

Published: May 03, 2016

Dominant spinal muscular atrophy is caused by mutations in BICD2, an important golgin protein.

Dominant spinal muscular atrophy is caused by mutations in BICD2, an important golgin protein.

Journal: Frontiers in neuroscience

Published: July 31, 2015

Dominant spinal muscular atrophy due to BICD2: a novel mutation refines the phenotype.

Dominant spinal muscular atrophy due to BICD2: a novel mutation refines the phenotype.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: December 17, 2013

Neuronal-specific deficiency of the splicing factor Tra2b causes apoptosis in neurogenic areas of the developing mouse brain.

Neuronal-specific deficiency of the splicing factor Tra2b causes apoptosis in neurogenic areas of the developing mouse brain.

Journal: PloS one

Published: October 30, 2013

Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathy.

Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathy.

Journal: Neuromuscular disorders : NMD

Published: August 28, 2013

Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy.

Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy.

Journal: American journal of human genetics

Published: March 19, 2013

Showing 1-9 of 9

Last Updated: 09/26/2026