S. Gross

Publication List Details

Period

1990 - 2008

Number

26

Co-Authors

Cross-talk towards the response regulator NtrC controlling nitrogen metabolism in Rhodobacter capsulatus (2006)

Drepper, T., Wiethaus, J., Giaourakis, D., Gross, S., Schubert, B., Vogt, M., ...

Rhodobacter capsulatus NtrB/NtrC two-component regulatory system controls expression of genes involved in nitrogen metabolism including urease and nitrogen fixation genes. The ntrY-ntrX genes, which...

Sex Pheromone of the Citrus Mealybug Planococcus citri: Synthesis and Optimization of Trap Parameters (2004)

A. Zada, E. Dunkelblum, M. Harel, F. Assael, S. Gross, Z. Mendel

A simple synthesis of the pheromone of the citrus mealybug, Planococcus citri (Risso) (Hemiptera: Pseudococcidae), has been developed. Various factors affecting capture of males have been assessed to...

Temporal Variation of the Processes and Interactions Among the Earth's Subsystems (1999)

J. Dickey, S. Gross

Seasonal variations in the Earth's gravitational field arc investigated through the analysis of I satellite laser ranging measurements and are compared with those produced by atmospheric mass...

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

Buiting, K, Dittrich, B, Gross, S, Lich, C, Färber, C, Buchholz, T, ...

The Prader-Willi syndrome (PWS) and the Angelman syndrome (AS) are caused by the loss of function of imprinted genes in proximal 15q. In approximately 2%-4% of patients, this loss of function is due...

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

Bürger, J, Buiting, K, Dittrich, B, Gross, S, Lich, C, Sperling, K, ...

Angelman syndrome (AS) is a neurogenetic disorder that appears to be caused by the loss of function of an imprinted gene expressed from maternal chromosome 15 only. Approximately 6% of patients have...

Structural analysis of inhibitor binding to human carbonic anhydrase II.

Boriack-Sjodin, P. A., Zeitlin, S., Chen, H. H., Crenshaw, L., Gross, S., Dantanarayana, A., ...

X-ray crystal structures of carbonic anhydrase II (CAII) complexed with sulfonamide inhibitors illuminate the structural determinants of high affinity binding in the nanomolar regime. The primary...

DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome.

Gillessen-Kaesbach, G, Gross, S, Kaya-Westerloh, S, Passarge, E, Horsthemke, B

Using a test based on parent of origin specific DNA methylation at the D15S63 (PW71) locus, we studied 385 patients (aged 1 to 36 years) for diagnostic confirmation of Prader-Willi syndrome (PWS) and...

Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples

Ludwig, M, Katalinic, A, Gross, S, Sutcliffe, A, Varon, R, Horsthemke, B

Recent case reports have suggested that infertility treatment with intracytoplasmic sperm injection (ICSI) may increase the risk of imprinting defects leading to Angelman syndrome (AS). Although...

Recurrent parotitis.

Cohen, H A, Gross, S, Nussinovitch, M, Frydman, M, Varsano, I

Recurrent parotitis in children is a well described but rare condition of unknown cause. The clinical features of 11 children with recurrent parotitis are described.

Polyneuritis following BCG re-vaccination

Katznelson, D., Gross, S., Sack, J.

A 12-year-old healthy, tuberculin negative boy was re-vaccinated with BCG. Nine days later symmetrical polyneuritis developed in all extremities. The tuberculin test was now strongly positive. It is...