Jorn Bullerdiek
Overview
Explore the profile of Jorn Bullerdiek including associated specialties, affiliations and a list of published articles.
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Articles
114
Citations
1662
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Recent Articles
1.
Bullerdiek J, Helmke B, Laban M
Mod Pathol
. 2022 Sep;
35(12):2029-2030.
PMID: 36153435
No abstract available.
2.
Bullerdiek J, Reisinger E, Rommel B, Dotzauer A
Protoplasma
. 2022 Apr;
259(6):1381-1395.
PMID: 35364749
There is no doubt that genetic factors of the host play a role in susceptibility to infectious diseases. An association between ABO blood groups and SARS-CoV-2 infection as well as...
3.
Bullerdiek J, Bock-Steinweg U
Gynakol Endokrinol
. 2021 Sep;
19(4):319-320.
PMID: 34539298
No abstract available.
4.
Volkner C, Liedtke M, Petters J, Lukas J, Murua Escobar H, Knuebel G, et al.
Stem Cell Res
. 2020 Dec;
50:102127.
PMID: 33360098
Niemann-Pick disease Type C (NPC) is a rare progressive neurodegenerative disorder with an incidence of 1:120,000 caused by mutations in the NPC1 or NPC2 gene leading to a massive cholesterol...
5.
Petters J, Volkner C, Krohn S, Murua Escobar H, Bullerdiek J, Reuner U, et al.
Stem Cell Res
. 2020 Nov;
49:102079.
PMID: 33197697
Wilson disease (WD) is a rare, monogenic disorder caused by mutations in the gene ATP7B. A loss of function of the expressed protein leads to excessive hepatic and cerebral copper...
6.
Volkner C, Liedtke M, Petters J, Huth K, Knuebel G, Murua Escobar H, et al.
Stem Cell Res
. 2020 Oct;
49:102056.
PMID: 33099109
Niemann-Pick disease type C1 (NPC1) is a rare inherited lipid storage disorder caused by mutations in the NPC1 gene. Mutations lead to impaired lipid trafficking and subsequently to accumulation of...
7.
Gottlieb A, Flor I, Nimzyk R, Burchardt L, Helmke B, Langenbuch M, et al.
Protoplasma
. 2020 Oct;
258(1):209-218.
PMID: 33034783
miRNAs of the largest human miRNA gene cluster at all, i.e., C19MC, are almost exclusively expressed in the placenta. Nevertheless, only little is known about the interindividual variation of their...
8.
Bullerdiek J, Rommel B
F1000Res
. 2019 Jan;
7:359.
PMID: 30647905
Mediator Complex Subunit 12 (MED12) is part of the transcriptional preinitiation machinery. Mutations of its gene predominantly occur in two types of highly frequent benign tumors, uterine leiomyomas and fibroadenomas...
9.
Holzmann C, Saager C, Mechtersheimer G, Koczan D, Helmke B, Bullerdiek J
Oncotarget
. 2018 Jul;
9(45):27595-27604.
PMID: 29963223
A 50 year old woman underwent laparoscopic supracervical hysterectomy because of symptomatic fibroids. Histologic examination of samples obtained after morcellation revealed typical uterine leiomyomas in all samples investigated. 28 and...
10.
Bloch J, Holzmann C, Koczan D, Helmke B, Bullerdiek J
Oncotarget
. 2017 Apr;
8(21):34762-34772.
PMID: 28410233
Uterine leiomyomas (UL) are the most prevalent symptomatic human tumors at all and somatic mutations of the gene encoding mediator subcomplex 12 (MED12) constitute the most frequent driver mutations in...