|
Factor XI
|
D005172 |
[Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C.
] |
|
Metapneumovirus
|
D029121 |
[A species of METAPNEUMOVIRUS causing a respiratory disease of high morbidity in turkeys.
, A METAPNEUMOVIRUS isolated from young children with acute RESPIRATORY TRACT INFECTIONS.
, A genus of the subfamily PNEUMOVIRINAE, containing two members: Turkey rhinotracheitis virus and a human Metapneumovirus. Virions lack HEMAGGLUTININ and NEURAMINIDASE.
] |
|
Basophils
|
A11.118.637.415.120 |
|
|
Spray Drying
|
E05.916.920 |
|
|
Orthoreovirus, Avian
|
D030101 |
[A species of ORTHOREOVIRUS infecting birds, with outcomes ranging from inapparent to lethal depending on the virus strain and age of the host bird. This species does not infect mammals.
] |
|
Refractive Surgical Procedures
|
E04.540.825 |
|
|
Trehalose
|
D09.698.629.305.880 |
|
|
Orthoreovirus, Mammalian
|
D030102 |
[A species of ORTHOREOVIRUS infecting mammals (other than baboons). There are four serotypes. In humans they are generally benign but may sometimes cause upper respiratory tract illness or enteritis in infants and children. MAMMALIAN ORTHOREOVIRUS 3 is a very pathogenic virus in laboratory rodents.
] |
|
Chromosomes, Artificial, P1 Bacteriophage
|
A11.284.187.178.195 |
|
|
Root Resorption
|
C07.793.901.653 |
|
|
Tooth Resorption
|
C07.793.901 |
|
|
Abnormalities, Multiple
|
C16.131.077 |
|
|
Congenital Abnormalities
|
C16.131 |
|
|
Chromosomes, Artificial, Mammalian
|
A11.284.187.178.190 |
|
|
Hyper-IgM Immunodeficiency Syndrome
|
C20.673.795.625 |
|
|
Parkinsonian Disorders
|
D020734 |
[A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.
] |
|
Guanine Nucleotide-Releasing Factor 2
|
D020735 |
[A 145-kDa guanine nucleotide exchange factor that is specific for rap1 and ras GTP-BINDING PROTEINS. It associates with SH3 domains of the crk family of signaling proteins.
] |
|
Cytogenetic Analysis
|
D020732 |
[Examination of CHROMOSOMES to diagnose, classify, screen for, or manage genetic diseases and abnormalities. Following preparation of the sample, KARYOTYPING is performed and/or the specific chromosomes are analyzed.
] |
|
DNA, A-Form
|
D044704 |
[An isoform of DNA that occurs in an environment rich in SODIUM and POTASSIUM ions. It is a right-handed helix with 11 base pairs per turn, a pitch of 0.256 nm per base pair and a helical diameter of 2.3 nm.
] |
|
Dipyridamole
|
D03.383.742.175 |
|
