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1
Structure Elucidation for MALDI Mass Spectrometry Imaging Using Infrared Ion Spectroscopy

von Schuurman, Jelle L. ; van Tetering, Lara ; Houthuijs, Kas J. ; et al.

Analytical Chemistry. 97(25):13160-13167
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2
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome

von Luo, Shiyu ; Gailus-Durner, Valérie ; McGivern, Bobbi ; et al.

European Journal of Human Genetics. 34(1):37-44
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3
NRAC controls CD36-mediated fatty acid uptake in adipocytes and lipid clearance in vivo

von Singh, Inderjeet ; Onogi, Yasuhiro ; Menezes, Filipe ; et al.

The EMBO Journal. 44(18):5037-5065
- Zum Volltext in PubMed Central
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4
Neuropathy-associated Tecpr2 mutation knock-in mice reveal endolysosomal loss of function phenotypes in neurons and microglia

von Bhattacharya, Debjani ; da Silva-Buttkus, Patricia ; Nalbach, Karsten ; et al.

Cell Death & Disease. 16(1)
- Zum Volltext in PubMed Central
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5
Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes

von Vo, Peter ; Imai-Leonard, Denise M. ; Yang, Benjamin ; et al.

BMC Genomics. 26(1)
- Zum Volltext in PubMed Central
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6
A fin-loop-like structure in GPX4 underlies neuroprotection from ferroptosis

von Lorenz, Svenja M. ; Wahida, Adam ; Bostock, Mark J. ; et al.

In Cell 8 January 2026 189(1):287-306
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7
Rethinking ratio-based normalization towards model-based approaches in heart weight analysis

von Oestereicher, Manuela A. ; da Silva-Buttkus, Patricia ; Gailus-Durner, Valerie ; et al.

Schlagworte: FALLACY; SIZE
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8
Correction: Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age

von Oestereicher, Manuela A. ; Ward, Christopher S. ; Schneltzer, Elida ; et al.

Frontiers in Cardiovascular Medicine ; volume 13 ; ISSN 2297-055X
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9
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism

von Gillet, Jean-Pierre ; Gerard, Louise ; Vieira, Wilfred ; et al.

In iScience 17 October 2025 28(10)
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10
Aminoadipate-semialdehyde synthase, a potential target for substrate reduction therapy in glutaric aciduria type 1

von Saad, Celine ; Jung-Klawitter, Sabine ; Dimitrov, Bianca ; et al.

Scientific Reports. 16(1)
- Zum Volltext in PubMed Central
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11
Understanding the Lifetime of Battery Cells Based on Solid-State Li6PS5Cl Electrolyte Paired with Lithium Metal Electrode

von Schlenker, Ruth ; Stępień, Dominik ; Koch, Pascal ; et al.

ACS Applied Materials & Interfaces. 12(17):20012-20025
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12
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

von Riedhammer, Korbinian M. ; Nguyen, Thanh-Minh T. ; Koşukcu, Can ; et al.

In Kidney International April 2024 105(4):844-864
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13
TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity

von Tollot-Wegner, Marie ; Jessen, Marco ; Kim, KyungMok ; et al.

Breast Cancer Research. 26(1)
- Zum Volltext in PubMed Central
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14
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes

von Hasenbein, Tim P. ; Hoelzl, Sarah ; Smith, Zachary D. ; et al.

Nature Communications. 15(1)
- Zum Volltext in PubMed Central
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15
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain

von Aguilar-Pimental, Juan A. ; Amarie, Oana V. ; Becker, Lore ; et al.

In Neuroscience Applied 2024 3
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16
Systematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal Dystrophies

von Briere, Andrew ; Vo, Peter ; Yang, Benjamin ; et al.

ISSN: 0146-0404.

Schlagworte: [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]
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17
Single-cell, whole-embryo phenotyping of mammalian developmental disorders

von Huang, Xingfan ; Henck, Jana ; Qiu, Chengxiang ; et al.

Nature: International weekly journal of science. 623(7988):772-781
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18
Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes

von Hang, Abraham ; Shao, Andy ; Shea, Michael ; et al.

ISSN: 0146-0404.

Schlagworte: inherited retinal disease; knockout animals; age-related macular degeneration; [SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs; [SDV.GEN]Life Sciences [q-bio]/Genetics
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19
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease

von Jacobs, Howard T. ; Szibor, Marten ; Rathkolb, Birgit ; et al.

In BBA - Molecular Basis of Disease October 2023 1869(7)
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20
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

von Calame, Daniel G. ; Guo, Tianyu ; Wang, Chen ; et al.

In The American Journal of Human Genetics 3 August 2023 110(8):1394-1413
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21
Standardized Pipeline for Metabolism and Cognition in GO‐DS21 Mouse Model: Investigating Down Syndrome Comorbidities.

von Selloum, Mohammed ; Silva‐Buttkus, Patricia da ; Riet, Fabrice ; et al.

Current Protocols; Jun2026, Vol. 6 Issue 6, p1-43, 43p
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22
GPR101 loss promotes insulin resistance and diet-induced obesity risk

von Garrett, Lillian ; Irmler, Martin ; Baljuls, Angela ; et al.

In Neuroscience Applied 2023 2
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23
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24
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice

von Oestereicher, Manuela A. ; Wotton, Janine M. ; Ayabe, Shinya ; et al.

Mammalian Genome: Precision and Functional Genomics. 34(2):180-199
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25
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome

von Maity-Kumar, Gandhari ; Ständer, Lisa ; DeAngelis, Meri ; et al.

In Molecular Metabolism December 2022 66
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