Suchergebnisse - "Abdelhamed, Zakia"

PubPharm (33)

1

Exogenous nitric oxide delivery protects against cardiopulmonary bypass-associated acute kidney injury : Histologic and serologic evidence from an ovine model

enthalten in: The Journal of thoracic and cardiovascular surgery | 2023

von Greenberg, J. | Hogue, S. | Raees, M. | +13

2

A novel hypomorphic allele ofSpag17causes primary ciliary dyskinesia phenotypes in mice

enthalten in: bioRxiv.org | 2022

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

3

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

4

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

5

Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants

enthalten in: PLoS genetics | 2019

von Snedeker, J. | Gibbons, W. | Paulding, D. | +3

6

Differential requirements of tubulin genes in mammalian forebrain development

enthalten in: PLoS genetics | 2019

von Bittermann, E. | Abdelhamed, Z. | Liegel, R. | +4

7

The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5

enthalten in: Scientific reports | 2019

von Abdelhamed, Z. | Abdelmottaleb, D. | El-Asrag, M. | +5

8

Characterization of Primary Cilia in Normal Fallopian Tube Epithelium and Serous Tubal Intraepithelial Carcinoma

enthalten in: International journal of gynecological cancer : official journal of the International Gynecological Cancer Society | 2018

von Abdelhamed, Z. | Ryan, T. | Fuller, M. | +9

9

A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice

enthalten in: Development (Cambridge, England) | 2018

von Abdelhamed, Z. | Vuong, S. | Hill, L. | +7

10

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

enthalten in: American journal of human genetics | 2015

von Logan, C. | Cossins, J. | Rodríguez Cruz, P. | +16