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Research article

First published 2004-02

No Association of Endometriosis With Glutathione S-Transferase M1 and T1 Null Mutations in a Japanese Population

Mayumi Morizane, Shigeki Yoshida, Satoshi Nakago [...]

Reproductive Sciences

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Research article

First published 2006-12

Management of a Patient With a Null Low-Density Lipoprotein Receptor Mutation

Genovefa D. Kolovou, George V.Z. Dedoussis, Katherine K. Anagnostopoulou [...]

Angiology

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Case report

First published 2011-5

Gaucher Disease with Prenatal Onset and Perinatal Death Due to Compound Heterozygosity for the Missense R131C and Null Rec Nci I GBA Mutations

April Goebl, Raechel A. Ferrier, Patrick Ferreira [...]

Pediatric and Developmental Pathology

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Research article

First published 2007-8

P105: Prevalence of a CNTF Null Mutation in Subjects with Tinnitus

Tobias Kleinjung, Birgit Fischer, Berthold Langguth [...]

Otolaryngology–Head and Neck Surgery

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Research article

First published 2010-3

Time course of retinal degeneration associated with the absence of 1,4,5-inositol trisphosphate receptor in Drosophila melanogaster

Olivia Vázquez-Martínez, Angélica Loranca, Lourdes Palma-Tirado [...]

Experimental Biology and Medicine

Free access

Research article

First published 2005-8

Null mutation of P53 attenuates hippocampal neuronal death in vivo following global ischemia in mice

Ichiro Yonekura, Nobutaka Kawahara, Akio Asai [...]

Journal of Cerebral Blood Flow & Metabolism

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Brief report

First published 2010-9-2

Genetic Deficiency of Plasma Lipoprotein-Associated Phospholipase A 2 (PLA2G7 V297F Null Mutation) and Risk of Alzheimer's Disease in Japan

Beena Koshy, Akinori Miyashita, Pamela St. Jean [...]

Journal of Alzheimer’s Disease

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Research article

First published 2025

Primary Uterine Angiosarcoma Presenting With Omental Metastasis,Lymph Node Involvement,and Demonstrating a Null p53 Mutational Staining Pattern

Jacob Rattin, Tatiana Buhtoiarova, Natalie Banet

International Journal of Surgical Pathology

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Research article

First published 2019-01-08

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

Gamze Guven, Başar Bilgic, Zeynep Tufekcioglu [...]

Journal of Alzheimer’s Disease

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Research article

First published 2011-1-7

A Novel Progranulin Mutation Causing Frontotemporal Lobar Degeneration with Heterogeneous Phenotypic Expression

Giacomina Rossi, Elena Piccoli, Luisa Benussi [...]

Journal of Alzheimer’s Disease

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