Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex

Ribosomopathies: human disorders of ribosome dysfunction

(2010) A. Narla et al.   BLOOD

When ribosomes go bad: diseases of ribosome biogenesis

(2010) Emily F. Freed et al.   Molecular BioSystems

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

(2010) Yutaka Shimomura et al.   NATURE

A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles

(2009) Muhammad Ayub et al.   AMERICAN JOURNAL OF HUMAN GENETICS

SOAP2: an improved ultrafast tool for short read alignment

(2009) R. Li et al.   BIOINFORMATICS

A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family

(2009) Chao Xu et al.   JOURNAL OF CUTANEOUS PATHOLOGY

A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis

(2009) Li-Qiong Cai et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

In situ expression of ribosomal protein L21 in developing tooth germ of the mouse lower first molar

(2009) Ming Xie et al.   JOURNAL OF MOLECULAR HISTOLOGY

How Common Are Extraribosomal Functions of Ribosomal Proteins?

(2009) Jonathan R. Warner et al.   MOLECULAR CELL

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation

(2008) Lynn Petukhova et al.   GENOMICS

Transcription by Moonlight: Structural Basis of an Extraribosomal Activity of Ribosomal Protein S10

(2008) Robert A. Weisberg   MOLECULAR CELL

G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

(2008) Sandra M Pasternack et al.   NATURE GENETICS

The YH database: the first Asian diploid genome database

(2008) G. Li et al.   NUCLEIC ACIDS RESEARCH