BbsI - NEB
BbsI has a High Fidelity version BbsI-HF ® (NEB #R3539). High Fidelity (HF) Restriction Enzymes have 100% activity in rCutSmart Buffer; single-buffer simplicity means more …
Bardet-biedl syndrome 1 | About the Disease | GARD
Bardet-Biedl syndrome (BBS) is an inherited condition that affects many parts of the body. People with this syndrome have progressive visual impairment due to cone-rod dystrophy; extra …
Bardet-Biedl Syndrome Overview - GeneReviews® - NCBI Bookshelf
2003年7月14日 · Bardet-Biedl syndrome (BBS) is a multisystem non-motile ciliopathy primarily characterized by retinal cone-rod dystrophy, obesity and related complications, postaxial …
Bardet-Biedl syndrome - MedlinePlus
Bardet-Biedl syndrome can result from mutations in at least 14 different genes (often called BBS genes). These genes are known or suspected to play critical roles in cell structures called cilia. …
Bardet-Biedl Syndrome - Symptoms, Causes, Treatment | NORD
2022年7月12日 · Bardet-Biedl syndrome (BBS) is a genetic condition that impacts multiple body systems. It is classically defined by six features. Patients with BBS can experience problems …
BBS1 gene - MedlinePlus
The BBS1 gene provides instructions for making a protein found in cells throughout the body. The BBS1 protein is part of a group (complex) of proteins that plays a critical role in the formation …
Bardet-Biedl Syndrome (BBS): Symptoms, Treatment - Healthline
2024年9月16日 · In white, Western populations, most cases of BBS are caused by alterations in the BBS1, BBS2, or BBS10 genes. Genetic testing can help identify the specific alteration …