HOXB1 — 카탈로그 3건
Gene HOXB1
NCBI Gene 3211
취급 제조사 2곳
국내 소싱 가능
3건
Activation of anterior HOX genes in hindbrain development during early embryogenesis
Congenital hereditary facial paralysis with variable hearing lossneurodegenerative diseasecongenital hereditary facial paralysis-variable hearing loss syndromehemoglobin measurementbody heighterythrocyte counthematocritdiastolic blood pressure change measurement
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Mice mutant for both Hoxa1 and Hoxb1 show extensive remodeling of the hindbrain and defects in craniofacial development. · Development (1999)HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice. · Am J Hum Genet (2012)The recruitment of SOX/OCT complexes and the differential activity of HOXA1 and HOXB1 modulate the Hoxb1 auto-regulatory enhancer function. · J Biol Chem (2001)
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