Keratosis pilaris/ulerythema ophryogenes and 18p deletion: Is it possible that the LAMA1 gene is involved? [7]

Journal of Medical Genetics

Volumn 38, Issue 2, 2001, Pages 127-128

  Zouboulis, C C ^a   Stratakis, C A ^a   Gollnick, H P M ^a   Orfanos, C E ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LAMININ; MESSENGER RNA;

ALLELE; CHROMOSOME 18P; CHROMOSOME DELETION; DISEASE ASSOCIATION; GENE EXPRESSION; GENE LOCATION; GENOME IMPRINTING; HUMAN; KERATINIZATION; KERATOSIS; KERATOSIS PILARIS; LETTER; PARTIAL MONOSOMY; PATHOGENESIS; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; GENE EXPRESSION REGULATION; HUMANS; KERATOSIS; LAMININ; MALE; SKIN;

EID: 0035104724     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (11)

1. Ulerythema ophryogenes and keratosis pilaris in a child with monosomy 18p
2. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome arrangements
3. Keratosis pilaris in a girl with monosomy 18p
4. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation
5. Human laminin A chain (LAMA) gene: Chromosomal mapping to locus 18p11.3
6. Primary structure of the human laminin A chain
7. A new nomenclature for the laminins
8. Molecular heterogeneity of basal laminae: Isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere
9. Laminin-1 and laminin-2 G-domain synthetic peptides bind syndecan-1 and are involved in acinar formation of a human submadibular gland cell line
10. Differential expression of laminin chains in the human major salivary gland
11. Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees