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Normdaten (Quelle GND / Entity Facts )

Zeineb Bakey

geboren 1982

Biografische Angaben
tätig an der Universität Pierre und Marie Curie Paris

Weiterführende Links

Gemeinsame Normdatei (GND) im Katalog der Deutschen Nationalbibliothek

Deutsche Digitale Bibliothek

Virtual International Authority File (VIAF)

International Standard Name Identifier (ISNI)

1

Cleavage of periostin by MMP9 protects mice from kidney cystic disease

Djaziri, Nabila (Verfasser)

Freiburg : Universität, 2024

E-Book

2

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

Bakey, Zeineb (Verfasser)

Freiburg : Universität, 2023

E-Book

3

A homozygous human WNT11 variant is associated with laterality, heart and renal defects

Berns, Henrike (Verfasser)

Freiburg : Universität, 2025

E-Book

4

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

Rad, Abolfazl (Verfasser)

Freiburg : Universität, 2019

E-Book

5

A 57 kB genomic deletion causing CTNS loss of function contributes to the CTNS mutational spectrum in the Middle East

Najafi, Maryam (Verfasser)

Freiburg : Universität, 2019

E-Book

6

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Loges, Niki Tomas (Verfasser)

Freiburg : Universität, 2020

E-Book

7

Parental whole-exome sequencing enables Sialidosis type II diagnosis due to an NEU1 missense mutation as an underlying cause of Nephrotic syndrome in the child

Maroofian, Reza (Verfasser)

Freiburg : Universität, 2023

E-Book

8

Spectrum of genetic variants in a cohort of 37 laterality defect cases

Antony, Dinu (Verfasser)

Freiburg : Universität, 2022

E-Book

9

Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

Rehman, Atteeq U. (Verfasser)

Freiburg : Universität, 2019

E-Book

10

Mutations in PIH1D3 cause X-linked primary ciliary dyskinesia with outer and inner dynein arm defects

Matter, Anja (Verfasser)

Freiburg : Universität, 2024

E-Book

11

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Riedhammer, Korbinian M. (Verfasser)

Freiburg : Universität, 2024

E-Book