The clinical spectrum of type IV collagen mutations
HH Lemmink, CH Schröder, LAH Monnens… - Human …, 1997 - Wiley Online Library
Clinical manifestations of type IV collagen mutations can vary from the severe, clinically and
genetically heterogeneous renal disorder, Alport syndrome, to autosomal dominant familial …
genetically heterogeneous renal disorder, Alport syndrome, to autosomal dominant familial …
Ceftriaxone-associated nephrolithiasis and biliary pseudolithiasis
RA De Moor, ACG Egberts, CH Schröder - European journal of pediatrics, 1999 - Springer
Biliary pseudolithiasis has been reported in patients who received ceftriaxone therapy. In
addition to biliary sludge formation occasional reports of ceftriaxone-induced nephrolithiasis …
addition to biliary sludge formation occasional reports of ceftriaxone-induced nephrolithiasis …
Identification of mutations in the α3 (IV) and α4 (IV) collagen genes in autosomal recessive Alport syndrome
T Mochizuki, HH Lemmink, M Mariyama, C Antignac… - Nature …, 1994 - nature.com
Alport syndrome (AS) is an hereditary disease of basement membranes characterized by
progressive renal failure and deafness. Changes in the glomerular basement membrane (GBM…
progressive renal failure and deafness. Changes in the glomerular basement membrane (GBM…
Hepatitis B virus genome is organized into nucleosomes in the nucleus of the infected cell
CT Bock, P Schranz, CH Schröder, H Zentgraf - Virus genes, 1994 - Springer
Hepatitis B virus (HBV) nucleoprotein complexes were isolated from nuclei of the human
hepatoblastoma cell line HepG2.2.15. Under conditions of physiological ionic strength, the …
hepatoblastoma cell line HepG2.2.15. Under conditions of physiological ionic strength, the …
Antivirals interacting with hepatitis B virus core protein and core mutations may misdirect capsid assembly in a similar fashion
HJ Hacker, K Deres, M Mildenberger… - Biochemical …, 2003 - Elsevier
Recently, heteroarylpyrimidines (HAP) have been identified as potent inhibitors of capsid
maturation. Here we discuss the HAP mode of action comparing the aggregation phenotype of …
maturation. Here we discuss the HAP mode of action comparing the aggregation phenotype of …
Expression of hepatitis B virus X protein in HBV-infected human livers and hepatocellular carcinomas
Q Su, CH Schröder, WJ Hofmann, G Otto… - Hepatology, 1998 - journals.lww.com
Transactivation of cellular genes and functional inactivation of p53 by the hepatitis B virus (HBV)
X gene-encoded protein (HBx) are proposed as alternative mechanisms for induction of …
X gene-encoded protein (HBx) are proposed as alternative mechanisms for induction of …
Mutations in the type IV collagen α3 (COL4A3) gene in autosomal recessive Alport syndrome
HH Lemmink, T MochlzukJ… - Human molecular …, 1994 - academic.oup.com
A group of 22 unrelated patients with sporadic or non-X-llnked Alport syndrome were screened
for mutations In the non-collagenous domain of the type IV collagen a3 (COL4A3) chain …
for mutations In the non-collagenous domain of the type IV collagen a3 (COL4A3) chain …
Inhibition of hepatitis B virus replication by drug-induced depletion of nucleocapsids
K Deres, CH Schroder, A Paessens, S Goldmann… - Science, 2003 - science.org
Chronic hepatitis B virus (HBV) infection is a major cause of liver disease. Only interferon-α
and the nucleosidic inhibitors of the viral polymerase, 3TC and adefovir, are approved for …
and the nucleosidic inhibitors of the viral polymerase, 3TC and adefovir, are approved for …
Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.
HH Lemmink, WN Nillesen, T Mochizuki… - The Journal of …, 1996 - Am Soc Clin Investig
Benign familial hematuria (BFH) is characterized by autosomal dominant inheritance, thinning
of the glomerular basement membrane (GBM) and normal renal function. It is frequent in …
of the glomerular basement membrane (GBM) and normal renal function. It is frequent in …
[HTML][HTML] Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation
FTL Van Der Loop, L Heidet, EDJ Timmer… - Kidney international, 2000 - Elsevier
Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation. Background
Alport syndrome (AS) is a clinically and genetically heterogeneous renal disorder, …
Alport syndrome (AS) is a clinically and genetically heterogeneous renal disorder, …
