Search results for: 'WA 0852 2611 9277 Harga Tukang Renovasi Plafon PVC 2 X 4 Kota Tangerang Selatan'
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Von Willebrand disease type 2 (VWF: c.4937A>G)
Test code: DOG-VWD2Von Willebrand disease is a condition that causes excessive bleeding due to a lack or reduced level of von Willebrand factor (vWF), a blood clotting protein.€49.85 -
Von Willebrand disease type 2 (VWF: c.1657T>G)
Test code: DOG-VWD2-BAVon Willebrand disease is a condition that causes excessive bleeding due to a deficiency or reduced levels of von Willebrand factor (vWF), a blood clotting protein.
This mutation is found in the Chinese Crested dog, but homozygous dogs do not appear to show clinical signs of bleeding disorders.
€49.85 -
Complete German Shepherd panel
Test code: DOG-BGALLThis panel includes the specific tests to be performed for the German Shepherd Dog: achromatopsia (DOG-ACHMB), Scott syndrome (DOG-CSS), coat length (DOG-LH), multidrug resistance (DOG-MDR1), mucopolysaccharidosis VII (DOG-MPS7), dwarfism (DOG-NAN), renal cystadenocarcinoma and nodular dermatofibrosis (DOG-RCND) and X-linked hypohidrotic ectodermal dysplasia (DOG-XHED).
€290.40 -
Hypocatalasia (CAT: c.979G>A)
Test code: DOG-HCHypocatalasia (or acatalasemia) is a rare genetic disorder caused by a mutation in the CAT gene, leading to a severe deficiency of catalase. This enzyme normally protects tissues against oxidative stress. The c.979G>A (p.Ala327Thr) mutation was first identified in a Beagle colony and subsequently detected in pet Beagles. A homozygous dog notably developed oral cavity gangrene with tooth loss at a young age. The disease may remain clinically silent for a long time, which highlights the importance of genetic screening in breeding dogs.
This test is also recommended for the Basset Hound as part of the Flemish government breeding program (see the official program).€49.85 -
PPARD – Endurance and performance in racing pigeons (PPARD: c.∗271C>T)
Test code: BIRD-PPARDThe PPARD gene is involved in mechanisms related to energy metabolism, fat utilisation and muscular endurance. In racing pigeons, a recent study suggests that certain variations in this gene may be linked to race performance, particularly return speed and ranking coefficient. The CC genotype for the PPARD c.*271C>T marker is the one that stands out most favourably in the study, notably because it was observed in pigeons taking part in a larger number of races. This test can therefore provide complementary information to guide the selection of breeding birds, without replacing the assessment of the pigeon, its lineage, training and actual racing results.
€49.85 -
Flanders Pack Required - French Bulldog
Test code: DOG-BULLFR-VLThis package includes the mandatory tests defined by the Flemish breeding program for French Bulldog: progressive retinal atrophy 4 (DOG-PRA-CRD4), canine multifocal retinopathy 1 (DOG-CMR1) and degenerative myelopathy 2 (DOG-DM2).
€175.45 -
Recommended Flanders Pack - Staffordshire Bull Terrier
Test code: DOG-STAFF-VL+This pack includes the recommended tests defined by the Flemish breeding program for Staffordshire Bull Terrier: Progressive retinal atrophy 4 (CORD1) (DOG-PRA-CRD4), Degenerative myelopathy 2 (DOG-DM2) and Cataract (DOG-HSF4-T).
€175.45 -
Recommended Flanders Pack - Bull Terrier
Test code: DOG-BULLT-VL+This pack includes the recommended tests defined by the Flemish breeding program for Bull Terrier: Degenerative myelopathy 2 (DOG-DM2), Progressive retinal atrophy 4 (CORD1) (DOG-PRA-CRD4), Primary lens luxation (DOG-PLL) and Progressive rod-cone degeneration (DOG-PRA-PRCD).
€211.75 -
Hypomyelination (FNIP2: c.880delA)
Test code: DOG-HYMNeurons are covered by a myelin sheath, in dogs with hypomyelination, the thickness of this sheath is reduced. The first symptoms are observed from the age of 1 to 2 weeks and include tremors and balance disorders. In most cases, the symptoms resolve after 3-4 months of age.
€49.85 -
Progressive retinal atrophy (PCARE: c.3149_3150insC)
Test code: DOG-PRA-RCD4Rod-cone dysplasia 4 is one of several forms of progressive retinal atrophy (PRA). This mutation leads to the late onset of PRA, with blindness occurring after 7 years of age.€49.85