Lztr1 | List of Frontiers open access articles

Brief Research Report

Published on 16 Jun 2021

Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon

in Epigenomics and Epigenetics

Mary Jo Talley
Diana Nardini
Nisha Shabbir
Lisa A. Ehrman
Carlos E. Prada
Ronald R. Waclaw

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2021.673995

5,548 views
2 citations

Brief Research Report

Published on 27 Aug 2024

LZTR1 loss-of-function variants associated with café au lait macules with or without freckling

in Pediatric Neurology

Svea Horn
Teresa Neuhann
Corina Hennig
Angela Abad-Perez
Eva-Christina Prott
Lisa Cardellini
Cornelia Potratz
Jonas Leubner
Birgit Eichhorn
Martin Merkel

Frontiers in Neurology

doi 10.3389/fneur.2024.1391425

4,918 views
1 citation

Case Report

Published on 18 Apr 2023

Case Report: Molecular autopsy underlie COVID-19-associated sudden, unexplained child mortality

in Primary Immunodeficiencies

Kana Unuma
Dan Tomomasa
Kosuke Noma
Kouhei Yamamoto
Taka-aki Matsuyama
Yohsuke Makino
Atsushi Hijikata
Shuheng Wen
Tsutomu Ogata
Nobuhiko Okamoto

Frontiers in Immunology

doi 10.3389/fimmu.2023.1121059

5,055 views
5 citations

Mini Review

Published on 16 Apr 2024

Gonadal dysfunction in a man with Noonan syndrome from the LZTR1 variant: case report and review of literature

in Reproduction

Francesca Orsolini
Luisa Pignata
Fulvia Baldinotti
Silvia Romano
Massimo Tonacchera
Domenico Canale

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1354699

5,037 views
4 citations

Original Research

Published on 17 Jan 2022

Identification of a Ubiquitin Related Genes Signature for Predicting Prognosis of Prostate Cancer

in Computational Genomics

Guoda Song
Yucong Zhang
Hao Li
Zhuo Liu
Wen Song
Rui Li
Chao Wei
Tao Wang
Jihong Liu
Xiaming Liu

Frontiers in Genetics

doi 10.3389/fgene.2021.778503

4,966 views
12 citations

Original Research

Published on 02 Oct 2024

Molecular diagnosis of patients with syndromic short stature identified by trio whole-exome sequencing

in Genetics of Common and Rare Diseases

Huihui Sun
Geng Zhang
Na Li
Xiangfang Bu

Frontiers in Genetics

doi 10.3389/fgene.2024.1399186

3,656 views
5 citations

Original Research

Published on 13 Jun 2022

Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome

in Genetics of Common and Rare Diseases

Ling Sun
Yu-mei Xie
Shu-shui Wang
Zhi-wei Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.915129

9,694 views
28 citations

Original Research

Published on 09 Apr 2024

Undiagnosed RASopathies in infertile men

in Reproduction

Anna-Grete Juchnewitsch
Kristjan Pomm
Avirup Dutta
Erik Tamp
Anu Valkna
Kristiina Lillepea
Eisa Mahyari
Stanislav Tjagur
Galina Belova
Viljo Kübarsepp

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1312357

6,248 views
9 citations

Articles

Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon

LZTR1 loss-of-function variants associated with café au lait macules with or without freckling

Case Report: Molecular autopsy underlie COVID-19-associated sudden, unexplained child mortality

Gonadal dysfunction in a man with Noonan syndrome from the LZTR1 variant: case report and review of literature

Identification of a Ubiquitin Related Genes Signature for Predicting Prognosis of Prostate Cancer

Molecular diagnosis of patients with syndromic short stature identified by trio whole-exome sequencing

Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome

Undiagnosed RASopathies in infertile men