Articles

Matrix metalloproteinase-9 involvement in the structural plasticity of dendritic spines

• Michal Stawarski
• Marzena Stefaniuk
• Jakub Wlodarczyk

Skeletal dysmorphology and mineralization defects in Fgf20 KO mice

in Bone Research

• Sylvie Dlugosova
• Frantisek Spoutil
• Carlos Eduardo Madureira Trufen
• Betul Melike Ogan
• Michaela Prochazkova
• Olha Fedosieieva
• Petr Nickl
• Goretti Aranaz Novaliches
• Radislav Sedlacek
• Jan Prochazka

Postnatal Craniofacial Skeletal Development of Female C57BL/6NCrl Mice

in Craniofacial Biology and Dental Research

• Xiaoxi Wei
• Neil Thomas
• Nan E. Hatch
• Min Hu
• Fei Liu

Neuroanatomical dysmorphology of the medial superior olivary nucleus in sudden fetal and infant death

in Brain Health and Clinical Neuroscience

• Anna Maria Lavezzi

Spine morphogenesis and synapse formation in tubular sclerosis complex models

in Neuroplasticity and Development

• Tadayuki Shimada
• Kanato Yamagata

Case Report: The success of face analysis technology in extremely rare genetic diseases in Korea: Tatton–Brown–Rahman syndrome and Say–Barber –Biesecker–Young–Simpson variant of ohdo syndrome

in Computational Genomics

• Sunha Park
• Jaewon Kim
• Tae-Young Song
• Dae-Hyun Jang

Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm

in Genetics of Common and Rare Diseases

• Eleanor G. Seaby
• Rodney D. Gilbert
• Gaia Andreoletti
• Reuben J. Pengelly
• Catherine Mercer
• David Hunt
• Sarah Ennis

Murine Models for the Study of Fetal Alcohol Spectrum Disorders: An Overview

in Pediatric Neurology

• Laura Almeida
• Vicente Andreu-Fernández
• Elisabet Navarro-Tapia
• Rosa Aras-López
• Mariona Serra-Delgado
• Leopoldo Martínez
• Oscar García-Algar
• María Dolores Gómez-Roig

Genetic diagnosis and clinical characteristics analysis of cardiospondylocarpofacial syndrome in a Chinese family

in Genetics of Common and Rare Diseases

• Qi Yang
• Qiang Zhang
• Sheng Yi
• Wurui Li
• Xunzhao Zhou
• Shujie Zhang
• Shang Yi
• Qinle Zhang
• Jingsi Luo

Novel variant alters splicing of TGFB2 in family with features of Loeys-Dietz syndrome

in Genetics of Common and Rare Diseases

• Emily R. Gordon
• Stephanie A. Felker
• Tanner F. Coleman
• Nadiya Sosonkina
• Jada Pugh
• Meagan E. Cochran
• Anna C. E. Hurst
• Sara J. Cooper

A novel frameshift variant in the MED13 gene causing intellectual developmental disorder-61 in a Chinese family

in Genetics of Common and Rare Diseases

• Qi Yang
• Qiang Zhang
• Sheng Yi
• Gaojie Huang
• Xunzhao Zhou
• Shang Yi
• Jingsi Luo

25 years into research with the Méhes Scale, a comprehensive scale of modern dysmorphology

in Schizophrenia

• Dalma Tényi
• Györgyi Csábi
• József Janszky
• Róbert Herold
• Tamás Tényi

Vitamin E stabilizes iron and mitochondrial metabolism in pulmonary fibrosis

in Respiratory Pharmacology

• Jing Chang
• Jiahui Wang
• Beibei Luo
• Weihao Li
• Ziyue Xiong
• Chaoqi Du
• Xue Wang
• Yuejiao Wang
• Jingya Tian
• Shuxin Li

Craniofacial development in patients of Tessier No.0 cleft with a bifid nose using 3D computed tomography

in Pediatric Surgery

• Xin Wang
• Huan Wang
• Jianjun You
• Ruobing Zheng
• Yihao Xu
• Fei Fan

Genetic Rodent Models of Obesity-Associated Ovarian Dysfunction and Subfertility: Insights into Polycystic Ovary Syndrome

in Systems Endocrinology

• Isabel Huang-Doran
• Stephen Franks

Analysis of Gene-Environment Interactions Related to Developmental Disorders

in Predictive Toxicology

• Yuhei Nishimura
• Kenji Kurosawa