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Showing 1 to 12 of 33 entries
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Characterization of the Olfactory Receptors Expressed in Human Spermatozoa.

Frontiers in molecular biosciences

Flegel C, Vogel F, Hofreuter A, Schreiner BS, Osthold S, Veitinger S, Becker C, Brockmeyer NH, Muschol M, Wennemuth G, Altmüller J, Hatt H, Gisselmann G.
PMID: 26779489
Front Mol Biosci. 2016 Jan 07;2:73. doi: 10.3389/fmolb.2015.00073. eCollection 2015.

The detection of external cues is fundamental for human spermatozoa to locate the oocyte in the female reproductive tract. This task requires a specific chemoreceptor repertoire that is expressed on the surface of human spermatozoa, which is not fully...

Role of noise in the initial stage of solidification instability.

Physical review. B, Condensed matter

Chou H, Cummins HZ, Muschol M, Qian XW.
PMID: 9948496
Phys Rev B Condens Matter. 1989 Feb 01;39(4):2529-2531. doi: 10.1103/physrevb.39.2529.

No abstract available.

Dendritic sidebranching with periodic localized perturbations: Directional solidification of pivalic acid-coumarin 152 mixtures.

Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics

Cummins HZ, Losert W, Muschol M, Qian X, Williams LM.
PMID: 9960612
Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics. 1993 Jul;48(1):489-499. doi: 10.1103/physreve.48.489.

No abstract available.

Outcome of patients with classical infantile pompe disease receiving enzyme replacement therapy in Germany.

JIMD reports

Hahn A, Praetorius S, Karabul N, Dießel J, Schmidt D, Motz R, Haase C, Baethmann M, Hennermann JB, Smitka M, Santer R, Muschol N, Meyer A, Marquardt T, Huemer M, Thiels C, Rohrbach M, Seyfullah G, Mengel E.
PMID: 25626711
JIMD Rep. 2015;20:65-75. doi: 10.1007/8904_2014_392. Epub 2015 Jan 28.

PURPOSE: Enzyme replacement therapy (ERT) has been shown to improve outcome in classical infantile Pompe disease. The purpose of this study was to assess mortality, morbidity, and shortcomings of ERT in a larger cohort of patients treated outside clinical...

Competing spatial and temporal instabilities in a globally coupled bistable semiconductor system near a codimension-two bifurcation.

Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics

Bose S, Rodin P, Scholl E.
PMID: 11088640
Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics. 2000 Aug;62(2):1778-89. doi: 10.1103/physreve.62.1778.

We study complex spatiotemporal dynamics in a globally coupled bistable reaction-diffusion model on a two-dimensional spatial domain. It is demonstrated that complex behavior appears near a codimension-two bifurcation point due to the competition of spatial and temporal instabilities. We...

Karhunen-Loeve local characterization of spatiotemporal chaos in a reaction-diffusion system.

Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics

Meixner M, Zoldi SM, Bose S, Scholl E.
PMID: 11046416
Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics. 2000 Feb;61(2):1382-5. doi: 10.1103/physreve.61.1382.

By computing the Karhunen-Loeve decomposition (KLD) correlation length xi(KLD) of a reaction-diffusion system in the extensive chaos regime, we show that it is a sensitive measure of spatial dynamical inhomogeneities. It reveals substantial spatial nonuniformity of the dynamics at...

Origin of metastable oligomers and their effects on amyloid fibril self-assembly.

Chemical science

Hasecke F, Miti T, Perez C, Barton J, Schölzel D, Gremer L, Grüning CSR, Matthews G, Meisl G, Knowles TPJ, Willbold D, Neudecker P, Heise H, Ullah G, Hoyer W, Muschol M.
PMID: 30079208
Chem Sci. 2018 Jun 13;9(27):5937-5948. doi: 10.1039/c8sc01479e. eCollection 2018 Jul 21.

Assembly of rigid amyloid fibrils with their characteristic cross-β sheet structure is a molecular signature of numerous neurodegenerative and non-neuropathic disorders. Frequently large populations of small globular amyloid oligomers (gOs) and curvilinear fibrils (CFs) precede the formation of late-stage...

Assessment of Peripheral Nervous System Alterations in Patients with the Fabry Related .

Diagnostics (Basel, Switzerland)

Godel T, V Cossel K, Friedrich RE, Glatzel M, Canaan-Kühl S, Duning T, Kronlage M, Heiland S, Bendszus M, Muschol N, Mautner VF.
PMID: 33266233
Diagnostics (Basel). 2020 Nov 30;10(12). doi: 10.3390/diagnostics10121027.

Background The purpose of this study is to examine alterations of the peripheral nervous system (PNS) in oligo-symptomatic patients carrying the Fabry related

Condyle morphology among patients with mucopolysaccharidosis: an observational study of panoramic radiographs.

International journal of paediatric dentistry

Schmid-Herrmann CU, Muschol N, Fuhrmann V, Koehn AF, Lezius S, Kahl-Nieke B, Koehne T.
PMID: 34967064
Int J Paediatr Dent. 2021 Dec 30; doi: 10.1111/ipd.12952. Epub 2021 Dec 30.

BACKGROUND: Mucopolysaccharidoses (MPS) are a group of rare metabolic diseases characterized by a wide spectrum of symptoms including progressive condylar resorption.AIM: The aim was to quantify the severity of condylar involvement in MPS I individuals in comparison to a...

A multicenter open-label extension study of intrathecal heparan-N-sulfatase in patients with Sanfilippo syndrome type A.

Molecular genetics and metabolism

Wijburg FA, Whitley CB, Muenzer J, Gasperini S, Del Toro M, Muschol N, Cleary M, Sevin C, Shapiro E, Alexanderian D.
PMID: 34247932
Mol Genet Metab. 2021 Sep-Oct;134(1):175-181. doi: 10.1016/j.ymgme.2021.07.001. Epub 2021 Jul 07.

Sanfilippo syndrome type A (mucopolysaccharidosis type IIIA) is a rare autosomal recessive lysosomal disorder characterized by deficient heparan-N-sulfatase (HNS) activity, and subsequent accumulation of heparan sulfate, especially in the central nervous system. The disease is associated with progressive neurodegeneration...

Clinical and Genetic Aspects of Juvenile Onset Pompe Disease.

Neuropediatrics

Holzwarth J, Minopoli N, Pfrimmer C, Smitka M, Borrel S, Kirschner J, Muschol N, Hartmann H, Hennermann JB, Neubauer BA, Hobbiebrunken E, Husain R, Hahn A.
PMID: 34852371
Neuropediatrics. 2021 Dec 01; doi: 10.1055/s-0041-1735250. Epub 2021 Dec 01.

Little is known about clinical symptomatology and genetics of juvenile onset Pompe disease (JOPD). The aims of this study were to analyze how these children are diagnosed, what clinical problems they have, and how phenotype is related to genotype....

Wave fronts may move upstream in semiconductor superlattices.

Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics

Carpio A, Bonilla LL, Wacker A, Scholl E.
PMID: 11031528
Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics. 2000 May;61(5):4866-76. doi: 10.1103/physreve.61.4866.

In weakly coupled, current biased, doped semiconductor superlattices, domain walls may move upstream against the flow of electrons. For appropriate doping values, a domain wall separating two electric-field domains moves downstream below a first critical current, it remains stationary...

Showing 1 to 12 of 33 entries