Anna-carina Weiss

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

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Found 28 publications

Polysialic acid regulates glomerular microvasculature formation by interaction with VEGF-A188 in mice.

Polysialic acid regulates glomerular microvasculature formation by interaction with VEGF-A188 in mice.

Journal: Angiogenesis

Published: August 26, 2024

Permissive ureter specification by TBX18-mediated repression of metanephric gene expression.

Permissive ureter specification by TBX18-mediated repression of metanephric gene expression.

Journal: Development (Cambridge, England)

Published: June 17, 2022

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

Journal: Journal of the American Society of Nephrology : JASN

Published: January 27, 2022

GATA6 is a crucial factor for Myocd expression in the visceral smooth muscle cell differentiation program of the murine ureter.

GATA6 is a crucial factor for Myocd expression in the visceral smooth muscle cell differentiation program of the murine ureter.

Journal: Development (Cambridge, England)

Published: January 12, 2022

Uridine diphosphate-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase deletion in mice leads to lethal intracerebral hemorrhage during embryonic development.

Uridine diphosphate-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase deletion in mice leads to lethal intracerebral hemorrhage during embryonic development.

Journal: Glycobiology

Published: May 20, 2021

Notch signaling is a novel regulator of visceral smooth muscle cell differentiation in the murine ureter.

Notch signaling is a novel regulator of visceral smooth muscle cell differentiation in the murine ureter.

Journal: Development (Cambridge, England)

Published: April 21, 2021

Rare heterozygous GDF6 variants in patients with renal anomalies.

Rare heterozygous GDF6 variants in patients with renal anomalies.

Journal: European journal of human genetics : EJHG

Published: March 20, 2020

Loss of Anks6 leads to YAP deficiency and liver abnormalities.

Loss of Anks6 leads to YAP deficiency and liver abnormalities.

Journal: Human molecular genetics

Published: February 01, 2020

Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies.

Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies.

Journal: Human molecular genetics

Published: January 28, 2020

Expansion of the renal capsular stroma, ureteric bud branching defects and cryptorchidism in mice with Wilms tumor 1 gene deletion in the stromal compartment of the developing kidney.

Expansion of the renal capsular stroma, ureteric bud branching defects and cryptorchidism in mice with Wilms tumor 1 gene deletion in the stromal compartment of the developing kidney.

Journal: The Journal of pathology

Published: November 09, 2019

A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification.

A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification.

Journal: Haematologica

Published: May 28, 2019

Growth differentiation factor 11 attenuates liver fibrosis via expansion of liver progenitor cells.

Growth differentiation factor 11 attenuates liver fibrosis via expansion of liver progenitor cells.

Journal: Gut

Published: March 29, 2019

Showing 1-12 of 28

Last Updated: 09/26/2026