Rare scleroderma autoantibodies to the U11 small nuclear ribonucleoprotein and to the trimethylguanosine cap of U small nuclear RNAs.

Por Gilliam, A C, Steitz, J A
Publicado em 1993

TRP Channel Gene Expression in the Mouse Retina

Por Gilliam, Jared C., Wensel, Theodore G.
Publicado em 2011

Perils of gene mapping with microsatellite markers.

Por Knowles, J A, Vieland, V J, Gilliam, T C
Publicado em 1992

PAGETOID RETICULOSIS IN A 5 YEAR OLD BOY

Por Miedler, John, Gould, Jennifer, Tamburro, Joan, Gilliam, Anita C.
Publicado em 2008

Granulomatous Periorificial Dermatitis: A Variant of Granulomatous Rosacea in Children?

Por Lucas, Chere R., Korman, Neil J., Gilliam, Anita C.
Publicado em 2009

Reciprocal product of a t(12;15) in murine plasmacytoma TEPC 1033:5' c-myc to IgH enhancer region.

Por Gilliam, A C, Fell, H P, Carayannopuolos, L, Tucker, P W
Publicado em 1989

“I FORGOT TO SHAVE MY HANDS”: A CASE OF SPINY KERATODERMA

Por Torres, Gisela, Behshad, Ramona, Han, Amy, Castrovinci, Anthony J, Gilliam, Anita C
Publicado em 2008

Disorders of Blood: II. The Heterozygous Sickle Cell States

Por Gilliam, J. C., Martin, Wilbur C., Preston, C. W., Henderson, A. B.
Publicado em 1963

Molecular and statistical approaches to the detection and correction of errors in genotype databases.

Por Brzustowicz, L M, Mérette, C, Xie, X, Townsend, L, Gilliam, T C, Ott, J
Publicado em 1993

Inactivation of the Vitamin D Receptor Enhances Susceptibility of Murine Skin to UV-induced Tumorigenesis

Por Ellison, Tara I., Smith, Molly K., Gilliam, Anita C., MacDonald, Paul N.
Publicado em 2008

Molecular genetics of human chromosome 4.

Por Gusella, J A, Gilliam, T C, MacDonald, M E, Cheng, S V, Tanzi, R E
Publicado em 1986

A Definitive Role of Ornithine Decarboxylase in Photocarcinogenesis

Por Ahmad, Nihal, Gilliam, Anita C., Katiyar, Santosh K., O’Brien, Thomas G., Mukhtar, Hasan
Publicado em 2001

Unusual Flexural Drug Reaction with Epidermal Pustules Associated with Adalimumab Treatment

Por Kristjansson, Arni K., Poulos, Georgann A., Chang, Timothy, Gilliam, Anita C., Cooper, Kevin D.
Publicado em 2008

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.

Por Selig, S, Bruno, S, Scharf, J M, Wang, C H, Vitale, E, Gilliam, T C, Kunkel, L M
Publicado em 1995

Illegitimate recombination generates a class switch from C mu to C delta in an IgD-secreting plasmacytoma.

Por Gilliam, A C, Shen, A, Richards, J E, Blattner, F R, Mushinski, J F, Tucker, P W
Publicado em 1984

Integration of multiscale dendritic spine structure and function data into systems biology models

Por Mancuso, James J., Cheng, Jie, Yin, Zheng, Gilliam, Jared C., Xia, Xiaofeng, Li, Xuping, Wong, Stephen T. C.
Publicado no Front Neuroanat (2014)

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

Por Ottman, R., Winawer, M.R., Kalachikov, S., Barker-Cummings, C., Gilliam, T.C., Pedley, T.A., Hauser, W.A.
Publicado em 2004

A Case of Churg-Strauss Syndrome Associated with Antiphospholipid Antibodies

Por Ferenczi, Katalin, Chang, Timothy, Camouse, Melissa, Han, Rujing, Stern, Robert, Willis, Joseph, Cooper, Kevin D., Gilliam, Anita C.
Publicado em 2006

Hair Follicle Stem Cell-Specific PPARγ Deletion Causes Scarring Alopecia

Por Karnik, Pratima, Tekeste, Zenar, McCormick, Thomas S., Gilliam, Anita C., Price, Vera H., Cooper, Kevin D., Mirmirani, Paradi
Publicado em 2008

Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.

Por Richards, J E, Gilliam, T C, Cole, J L, Drumm, M L, Wasmuth, J J, Gusella, J F, Collins, F S
Publicado em 1988