Steve C Huang

发表

Non-islet origin of pancreatic islet cell tumors.

A. Vortmeyer, I. Lubensky, Steve Huang, 2004, The Journal of clinical endocrinology and metabolism.

Mutations of the MEN1 tumor suppressor gene in pituitary tumors.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas.

F. Collins, M. Emmert-Buck, A. Vortmeyer, 1997, Cancer research.

From tissue phenotype to proteotype: sensitive protein identification in microdissected tumor tissue.

Griffin P Rodgers, Jingqi Lei, Youn-Soo Lee, 2006, International journal of oncology.

Memory of Extracellular Adenosine A2A Purinergic Receptor-mediated Signaling in Murine T Cells*

Steve Huang, M. Sitkovsky, M. Koshiba, 1997, The Journal of Biological Chemistry.

This PDF file includes: Materials and Methods

Robert B. Hartlage, W. C. Banyai, Jessica C. Ebert, 2009 .

Identification of APC gene mutations in colorectal cancer using universal microarray‐based combinatorial sequencing‐by‐hybridization

R. Drmanac, P. Fortina, S. Surrey, 2004, Human mutation.

Loss of heterozygosity of chromosome 1q in gastrinomas: occurrence and prognostic significance.

A. Vortmeyer, R. Jensen, Steve Huang, 2003, Cancer research.

Loss of Heterozygosity of Chromosome 1 q in Gastrinomas : Occurrence and Prognostic Significance

A. Vortmeyer, R. Jensen, Steve Huang, 2003 .

Role of A2a Extracellular Adenosine Receptor-Mediated Signaling in Adenosine-Mediated Inhibition of T-Cell Activation and Expansion

Steve Huang, M. Sitkovsky, M. Koshiba, 1997 .

Studies of expression and possible functional role of purinergic receptors in cell‐mediated immunity: Experimental approaches, controls, and caveats

J. Armstrong, Steve Huang, M. Sitkovsky, 1998 .

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma

A. Vortmeyer, G. Chrousos, Steve Huang, 2002, Oncogene.

Combinatorial sequencing-by-hybridization: analysis of the NF1 gene.

R. Drmanac, P. Fortina, S. Surrey, 2006, Genetic testing.

Protein patterns and proteins that identify subtypes of glioblastoma multiforme

A. Vortmeyer, I. Lubensky, R. Weil, 2004, Oncogene.

Role of A2a extracellular adenosine receptor-mediated signaling in adenosine-mediated inhibition of T-cell activation and expansion.

M. Sitkovsky, M. Koshiba, S. Apasov, 1997, Blood.

Proteomic profiling of von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 pheochromocytomas reveals different expression of chromogranin B.

Deric M. Park, A. Vortmeyer, W. Linehan, 2007, Endocrine-related cancer.

Multiplexed SNP genotyping using nanobarcode particle technology

Radoje Drmanac, Snezana Drmanac, Chongjun Xu, 2006, Analytical and bioanalytical chemistry.

Allelic imbalance of the mutant and wild-type RET allele in MEN 2A-associated medullary thyroid carcinoma

A. Vortmeyer, G. Chrousos, Steve Huang, 2001, Oncogene.

Amplification and overexpression of mutant RET in multiple endocrine neoplasia type 2-associated medullary thyroid carcinoma.

A. Vortmeyer, I. Lubensky, Steve Huang, 2003, The Journal of clinical endocrinology and metabolism.

Do somatic RET mutations represent a phenomenon of tumor progression

A. Vortmeyer, G. Chrousos, K. Pacak, 2001 .

Multiple leiomyomas of the esophagus, lung, and uterus in multiple endocrine neoplasia type 1.

A. Vortmeyer, I. Lubensky, M. Skarulis, 2001, The American journal of pathology.

A patient with MEN 2 and multiple mutations of RET in the germline.

A. Vortmeyer, G. Chrousos, Steve Huang, 2000, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Somatic von Hippel-Lindau gene mutations detected in sporadic endolymphatic sac tumors.

A. Vortmeyer, Steve Huang, E. Oldfield, 2000, Cancer research.

Advances in Brief Somatic von Hippel-Lindau Gene Mutations Detected in Sporadic Endolymphatic Sac Tumors 1

A. Vortmeyer, Steve Huang, E. Oldfield, 2000 .

Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion

A. Vortmeyer, I. Lubensky, Steve Huang, 2002, Oncogene.

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas.

I. Lubensky, G. Chrousos, K. Pacak, 2000, Cancer research.