Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

307 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Orchestration of human multi-lineage hematopoietic cell development by humanized in vivo bone marrow models.
Renou L, Sun W, Friedrich C, Galant K, Conrad C, Consalus A, Plantier E, Schallmoser K, Krisch L, Barroca V, Devanand S, Dechamps N, Reinisch A, Martinovic J, Magnani A, Faivre L, Lewandowski D, Calvo J, Perie L, Kosmider O, Pflumio F. Renou L, et al. Among authors: martinovic j. Hemasphere. 2025 Apr 22;9(4):e70120. doi: 10.1002/hem3.70120. eCollection 2025 Apr. Hemasphere. 2025. PMID: 40265169 Free PMC article.
Histologic and molecular features shared between antibody-mediated rejection of kidney allografts and chronic histiocytic intervillositis support common pathogenesis.
Albersammer L, Leon J, Martinovic J, Dagobert J, Lebraud E, Bessières B, Loeuillet L, Eloudzeri M, Vivanti AJ, Dumery G, Marchaudon V, Antal C, Korganow AS, Quibel T, Costedoat-Chalumeau N, Tsatsaris V, Benachi A, Zuber J, Rabant M. Albersammer L, et al. Among authors: martinovic j. J Pathol. 2025 Jun;266(2):177-191. doi: 10.1002/path.6413. Epub 2025 Apr 3. J Pathol. 2025. PMID: 40178007 Free PMC article.
Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity.
Coste T, Aloui C, Chanclud J, Blondiaux E, Martinovic J, Attie-Bitach T, Petit F, Héron D, de Brevern AG, Radjasandirane R, Corpechot M, Morel H, Petermann R, Leutenegger AL, Tournier-Lasserve E. Coste T, et al. Among authors: martinovic j. Prenat Diagn. 2025 Jan 6. doi: 10.1002/pd.6743. Online ahead of print. Prenat Diagn. 2025. PMID: 39763161
307 results