G Lubec|N Getoff - JoVE Visualize

Showing results (121-130 of 319) with videos related to

Pageof 32

Sort By:

Zeitschrift Fur Hautkrankheiten|November 15, 1979

[Excretion of acid mucopolysaccharides in the urine and sweat in hereditary bullous epidermolysis]E Ratzenhofer, E Legenstein, E Meznik, et al.

Monatsschrift Fur Kinderheilkunde|October 1, 1979

[A contribution to hereditary sensory neuropathy. Electron microscopical studies (author's transl)]D Lachmann, G Lassmann, G Lubec, et al.

Neuroscience Letters|August 22, 1997

Evidence against increased glycoxidation in patients with Alzheimer's diseaseR Seidl, E Schuller, N Cairns, et al.

Life Sciences|January 1, 1997

Excitatory amino acids and monoamines in parahippocampal gyrus and frontal cortical pole of adults with Down syndromeD Risser, G Lubec, N Cairns, et al.

Journal of Neural Transmission. Supplementum|January 5, 2002

Protein levels of human peroxiredoxin subtypes in brains of patients with Alzheimer's disease and Down syndromeS H Kim, M Fountoulakis, N Cairns, et al.

Cellular and Molecular Life Sciences : CMLS|December 29, 2000

Decreased levels of complex III core protein 1 and complex V beta chain in brains from patients with Alzheimer's disease and Down syndromeS H Kim, R Vlkolinsky, N Cairns, et al.

Electrophoresis|February 24, 2001

Changes of voltage-dependent anion-selective channel proteins VDAC1 and VDAC2 brain levels in patients with Alzheimer's disease and Down syndromeB C Yoo, M Fountoulakis, N Cairns, et al.

Padiatrie Und Padologie|January 1, 1988

The determination of urinary 3-trans-hydroxyproline (3 OHP). II. Normal values in neonates, infants and preschool childrenM T Weiss, M Weninger, J Häusler, et al.

Journal of Neural Transmission. Supplementum|February 10, 2000

c-fos expression in brains of patients with Down syndromeS Greber-Platzer, B Balcz, N Cairns, et al.

Journal of Neural Transmission. Supplementum|February 10, 2000

Differential display reveals deteriorated mRNA levels of NADH3 (complex I) in cerebellum of patients with Down syndromeK Krapfenbauer, B C Yoo, N Cairns, et al.

Pageof 32

Showing results (121-130 of 319) with videos related to

Sort By:

Pageof 32

Zeitschrift Fur Hautkrankheiten|November 15, 1979

[Excretion of acid mucopolysaccharides in the urine and sweat in hereditary bullous epidermolysis]E Ratzenhofer, E Legenstein, E Meznik, et al.

Monatsschrift Fur Kinderheilkunde|October 1, 1979

[A contribution to hereditary sensory neuropathy. Electron microscopical studies (author's transl)]D Lachmann, G Lassmann, G Lubec, et al.

Neuroscience Letters|August 22, 1997

Evidence against increased glycoxidation in patients with Alzheimer's diseaseR Seidl, E Schuller, N Cairns, et al.

Life Sciences|January 1, 1997

Excitatory amino acids and monoamines in parahippocampal gyrus and frontal cortical pole of adults with Down syndromeD Risser, G Lubec, N Cairns, et al.

Journal of Neural Transmission. Supplementum|January 5, 2002

Protein levels of human peroxiredoxin subtypes in brains of patients with Alzheimer's disease and Down syndromeS H Kim, M Fountoulakis, N Cairns, et al.

Cellular and Molecular Life Sciences : CMLS|December 29, 2000

Decreased levels of complex III core protein 1 and complex V beta chain in brains from patients with Alzheimer's disease and Down syndromeS H Kim, R Vlkolinsky, N Cairns, et al.

Electrophoresis|February 24, 2001

Changes of voltage-dependent anion-selective channel proteins VDAC1 and VDAC2 brain levels in patients with Alzheimer's disease and Down syndromeB C Yoo, M Fountoulakis, N Cairns, et al.

Padiatrie Und Padologie|January 1, 1988

The determination of urinary 3-trans-hydroxyproline (3 OHP). II. Normal values in neonates, infants and preschool childrenM T Weiss, M Weninger, J Häusler, et al.

Journal of Neural Transmission. Supplementum|February 10, 2000

c-fos expression in brains of patients with Down syndromeS Greber-Platzer, B Balcz, N Cairns, et al.

Journal of Neural Transmission. Supplementum|February 10, 2000

Differential display reveals deteriorated mRNA levels of NADH3 (complex I) in cerebellum of patients with Down syndromeK Krapfenbauer, B C Yoo, N Cairns, et al.

Pageof 32