Results 111 to 120 of about 13,838 (187)

A Homozygous Dab1-/- Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract. [PDF]

open access: yesBiomolecules, 2021
Racetin A   +11 more
europepmc   +1 more source

Subtype- and Site-Specific Innervation of Melanocytic Nevi as Revealed by PGP 9.5 and CGRP Expression. [PDF]

open access: yesMedicina (Kaunas)
Minigo B   +8 more
europepmc   +1 more source

Connexin Expression Is Altered in Liver Development of Yotari (dab1 -/-) Mice. [PDF]

open access: yesInt J Mol Sci, 2021
Paštar V   +6 more
europepmc   +1 more source

Emotion dataset from Indonesian public opinion. [PDF]

open access: yesData Brief, 2022
Riccosan   +3 more
europepmc   +1 more source

Expression of FGF23 and α-KLOTHO in Normal Human Kidney Development and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT). [PDF]

open access: yesBiomolecules
Bajt P   +9 more
europepmc   +1 more source

Loss of <i>Dab1</i> Alters Expression Patterns of Endocytic and Signaling Molecules During Embryonic Lung Development in Mice. [PDF]

open access: yesLife (Basel)
Todorović P   +8 more
europepmc   +1 more source

Immunohistochemical Expression of TNFR1, IL-6, and TGF-β1 in the Synovial Tissue of Patients with Hip Osteoarthritis. [PDF]

open access: yesBiomedicines
Todorović P   +7 more
europepmc   +1 more source

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