Results 161 to 170 of about 1,877 (178)

AR3-Jacklyn20130701M-M39.txt

2013
openaire   +1 more source

Comments on the results of the preceding publication of Manigault concerning Agrobacterium tumefaciens M39 mutant

Mutation Research, 1970
J, De Ley, J B, van der Plaat
openaire   +2 more sources

Phenotypic expression of Bardet–Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene

Vision Research, 2012
Alessandro Iannaccone, Darryl Nishimura, Val Sheffield   +2 more
exaly  

A knockin mouse model of the Bardet–Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

Proceedings of the National Academy of Sciences of the United States of America, 2007
Kamal Rahmouni, Robert Mullins, Darryl Nishimura   +2 more
exaly  

M39 CHILDHOOD ADOPTION AND BODY COMPOSITION IN ADULTHOOD: THE ROLE OF GENETIC CONFOUNDING IN CONTEXT OF ANOREXIA NERVOSA

European Neuropsychopharmacology, 2019
Avina Hunjan, Rosa Cheesman, Christopher Hübel, Jonathan Coleman, Thalia Eley, Gerome Breen   +5 more
openaire   +1 more source

Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease

Human Molecular Genetics, 2019
Andrew Singleton, Cornelis Blauwendraat, Blauwendraat Cornelis   +2 more
exaly  

M39 – Pubertal Disruption in Chronic Inflammatory Disease

2012
openaire   +1 more source

Osteoarthritis-Like Changes in Bardet–Biedl Syndrome Mutant Ciliopathy Mice (Bbs1M390R/M390R): Evidence for a Role of Primary Cilia in Cartilage Homeostasis and Regulation of Inflammation

Frontiers in Physiology, 2018
David L Kooyman, Val Sheffield, Brandon Rose   +2 more
exaly  

M39 – Risk Assessment Monitoring Bone Markers/Osteoporosis

2013
openaire   +1 more source

Spectral types in the open cluster M 39.

Publications of the Astronomical Society of the Pacific, 1976
exaly