Suchergebnisse - "Spiegel, A M"

PubPharm (333)

1

Functional Effects of Monoclonal Antibodies to the Purified Amino-Terminal Extracellular Domain of the Human Ca2+ Receptor - We generated three functionally unique monoclonal antibodies to the purified human CaR extracellular domain. Flow cytometry studies of chimeric receptors localized their epitopes to lobe 2 of the VFT domain. These results lead us to propose a mechanism for the functional effects of these antibodies.

enthalten in: Journal of bone and mineral research | 2007

von Hu, J. | Reyes-Cruz, G. | Goldsmith, P. | +3

2

Degradation of the non-palmitoylated invertebrate visual guanine-nucleotide binding protein, iGq&agr;(C3,4A), by the ubiquitin-proteasomal pathway is regulated by its activation and translocation to the cytoplasm

enthalten in: Visual neuroscience | 2007

von Go, L. | Mitchell, J. | Bamsey, C. | +16

3

Menin molecular interactions : insights into normal functions and tumorigenesis

enthalten in: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme | 2005

von Agarwal, S. | Kennedy, P. | Scacheri, P. | +15

4

Menin Molecular Interactions: Insights into Normal Functions and Tumorigenesis

in: Hormone and metabolic research | 2005

von Agarwal, S. | Kennedy, P. | Scacheri, P. | +15

5

Menin Molecular Interactions: Insights into Normal Functions and Tumorigenesis

in: Hormone and metabolic research | 2005

von Agarwal, S. | Kennedy, P. | Scacheri, P. | +15

6

Executive summary of the Strategic Plan for National Institutes of Health Obesity Research.

enthalten in: The American journal of clinical nutrition | 2005

von Spiegel, A. | Alving, B.

7

Gland size is associated with changes in gene expression profiles in sporadic parathyroid adenomas

enthalten in: Annals of surgical oncology | 2004

von Rosen, J. | Costouros, N. | Lorang, D. | +7

8

Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino-Terminus of the Human Calcium Receptor - To define the molecular pathogenesis of severe postnatal hypocalcemia in monozygotic twin sisters, we sequenced their CaR gene and identified a missense mutation, K29E. Expression of the mutant receptor in vitro showed a marked increase in Ca2+ sensitivity explaining the observed phenotype. Additional mutagenesis studies lead us to speculate concerning a novel mechanism whereby the K29E mutation may lead to receptor activation.

enthalten in: Journal of bone and mineral research | 2004

von Hu, J. | Mora, S. | Weber, G. | +3

9

ORIGINAL ARTICLES - Autosomal Dominant Hypocalcemia Caused by a Novel Mutation in the Loop 2 Region of the Human Calcium Receptor Extracellular Domain

enthalten in: Journal of bone and mineral research | 2002

von Hu, J. | Mora, S. | Colussi, G. | +6

10

Hyperparathyroidism in Hereditary Syndromes: Special Expressions and Special Managements

enthalten in: Journal of bone and mineral research | 2002

von Marx, S. | Simonds, W. | Agarwal, S. | +11

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[34]