Anagram & Information om | Engelska ordet PKD


PKD

2
DKP
PDK

Antal bokstäver

3

Är palindrom

Nej

2
KD
PK

1

1

9
DK
DKP
DP
KD
KP
PD
PDK
PK


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Exempel på hur man kan använda PKD i en mening

  • Philip Kindred Dick (December 16, 1928 – March 2, 1982), often referred to by his initials PKD, was an American science fiction writer and novelist.
  • They have two sensors on top of the traffic lights (pedestrian crossing detector; PCD, and pedestrian kerb detector; PKD).
  • Immediately after the end of the war, there were four such stations in the Dutch East Indies, and these were all designated with callsigns in the new PK series: PKA Sabang, PKB Weltevreden, PKC Sitoebondo, and PKD Koepang'.
  • It is the cause of proliferative kidney disease (PKD), one of the most serious parasitic diseases of salmonid populations in Europe and North America that can result in losses of up to 90% in infected populations.
  • She prioritizes specific conditions, including polycystic kidney disease (PKD), skin abnormalities, structural defects, and inherited blindness.
  • There are three different subtypes of PD that include paroxysmal kinesigenic dyskinesia (PKD), paroxysmal nonkinesigenic dyskinesia (PNKD), and paroxysmal exercise-induced dystonia (PED).
  • Paroxysmal kinesigenic dyskinesia (PKD), also called paroxysmal kinesigenic choreoathetosis (PKC), is a rare hyperkinetic movement disorder of the paroxysmal dyskinesias characterized by attacks (paroxysms) of involuntary movements, which are triggered by sudden voluntary movements.
  • PED differs from two closely related disorders, for example paroxysmal kinesogenic dyskinesia (PKD) and paroxysmal nonkinesigenic dyskinesia (PNKD), based on what brings on the symptoms, namely prolonged exercise, such as brisk walking or running for at least 10 minutes.
  • PKD results from defects in the primary cilium, an immotile, hair-like cellular organelle present on the surface of most cells in the body, anchored in the cell body by the basal body.
  • For example, the PKD-dependent association of Rap1 with C3G suggests that PKD may be critical for localizing Rap1 not only with integrins but also with Rap1 GEFs.
  • As of 2019 Kadmon had ongoing clinical trials for Belumosudil in specific fibrotic and neurodegenerative diseases and tesevatinib to treat autosomal dominant polycystic kidney disease (PKD) and autosomal recessive PKD.
  • According to the UniProt description, polycystin 1 contains 16 polycystic kidney disease (PKD) domains, one LDL-receptor class A domain, one C-type lectin family domain, and 16-18 putative TMSs in positions between residues 2200 and 4100.


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