Scd1ab-Xyk: A new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse

Molecular Genetics and Genomics

Volumn 272, Issue 2, 2004, Pages 129-137

  Lu, Y ^a,b   Bu, L ^a,b   Zhou, S ^c   Jin, M ^b   Sundberg, J P ^d   Jiang, H ^a,b   Qian, M ^a,b   Shi, Y ^a,b   Zhao, G ^f   Kong, X ^a,b,e   Hu, L ^a,b  

^a Shanghai Jiao Tong University Affiliated Sixth People s Hospital   (China)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^c PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^d JACKSON LABORATORY   (United States)

^e State Key Lab of Medical Genomics   (China)

^f NONE

Author keywords

Hair follicle; Hair loss; Mutation; Sebaceous gland hypoplasia; Skin

Indexed keywords

ACYL COENZYME A DESATURASE; GENE PRODUCT; PROLINE; PROTEIN SCD1; STEAROYL COENZYME A DESATURASE 1; TRINUCLEOTIDE; UNCLASSIFIED DRUG; DNA; SCD1 PROTEIN, MOUSE;

ALLELISM; ALOPECIA; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DELETION MUTANT; EXON; FEMALE; GENE; GENE FUNCTION; GENE INSERTION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; HAIR DISEASE; HAIR FOLLICLE; HAPLOTYPE; HISTOLOGY; MALE; MOUSE; NONHUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGENY; PROTEIN STRUCTURE; SCAR FORMATION; SCD1 AB XYK GENE; SEBACEOUS GLAND; SKIN DEFECT; ALLELE; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; CHROMOSOME MAP; CONGENITAL MALFORMATION; CONGENITAL SKIN DISEASE; DISEASE MODEL; ENZYMOLOGY; GENETICS; HAIR; HUMAN; MOLECULAR GENETICS; MOUSE MUTANT; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY;

ANIMALIA; INSERTION SEQUENCES;

ALLELES; ALOPECIA; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DISEASE MODELS, ANIMAL; DNA; EXONS; HAIR; HAPLOTYPES; HUMANS; MICE; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEBACEOUS GLANDS; SEQUENCE HOMOLOGY, AMINO ACID; SKIN ABNORMALITIES; STEAROYL-COA DESATURASE;

EID: 5644277720     PISSN: 16174615     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00438-004-1043-3     Document Type: Article

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