Suchergebnisse - "Lukacs, Marshall"

PubPharm (13)

1

A novel hypomorphic allele ofSpag17causes primary ciliary dyskinesia phenotypes in mice

enthalten in: bioRxiv.org | 2022

von Abdelhamed, Z. | Lukacs, M. | Cindric, S. | +2

2

Severe Biallelic Loss-of-function Mutations inNicotinamide Mononucleotide Adenylyltransferase 2 (NMNAT2)in Two Fetuses with Fetal Akinesia Deformation Sequence

enthalten in: bioRxiv.org | 2022

von Lukacs, M. | Gilley, J. | Zhu, Y. | +9

3

Glycosylphosphatidylinositol Biosynthesis and Remodeling are Required for Neural Crest Cell, Cardiac and Neural Development

enthalten in: bioRxiv.org | 2022

von Lukacs, M. | Roberts, T. | Chatuverdi, P. | +1

4

Correction : A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

enthalten in: Disease models & mechanisms | 2021

von Abdelhamed, Z. | Lukacs, M. | Cindric, S. | +3

ErratumFor: Dis Model Mech. 2020 Oct 30;13(10):. - PMID 32988999

5

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

enthalten in: Disease models & mechanisms | 2020

von Abdelhamed, Z. | Lukacs, M. | Cindric, S. | +3

ErratumIn: Dis Model Mech. 2021 Jan 1;14(1):. - PMID 34115122

6

CNS glycosylphosphatidylinositol deficiency results in delayed white matter development, ataxia and premature death in a novel mouse model

enthalten in: Human molecular genetics | 2020

von Lukacs, M. | Blizzard, L. | Stottmann, R.

7

Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence

enthalten in: Experimental neurology | 2019

von Lukacs, M. | Gilley, J. | Zhu, Y. | +9

8

CNS Glycosylphosphatidylinositol Deficiency Results in Delayed White Matter Development, Ataxia, and Premature Death in a Novel Mouse Model

enthalten in: bioRxiv.org | 2019

von Lukacs, M. | Stottmann, R.

9

Glycosylphosphatidylinositol biosynthesis and remodeling are required for neural tube closure, heart development, and cranial neural crest cell survival

enthalten in: eLife | 2019

von Lukacs, M. | Roberts, T. | Chatuverdi, P. | +1

10

Congenital Cataracts and Gut Dysmotility in a DYNC1H1 Dyneinopathy Patient

enthalten in: Genes | 2016

von Gelineau-Morel, R. | Lukacs, M. | Weaver, K. | +3