A. A. Pannett

发表

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1.

C. Larsson, B. Teh, S. Forbes, 1998, Genomics.

Menin interacts directly with the homeobox-containing protein Pem.

C. Larsson, F. Piehl, W. V. D. Van de Ven, 2001, Biochemical and biophysical research communications.

Mapping of the gene encoding the B56β subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)

C. Larsson, S. Forbes, B. Harding, 1997, Human Genetics.

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.

R. Thakker, M. Whyte, P. Dixon, 1999, American journal of human genetics.

MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO).

C. López-Otín, S. Krane, B. Harding, 2005, The Journal of clinical investigation.

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions

R. Thakker, R. Domingues, L. Sobrinho, 2002, Clinical endocrinology.

MMP 13 mutation causes spondyloepimetaphyseal dysplasia , Missouri type ( SEMDMO )

C. López-Otín, S. Krane, B. Harding, 2005 .

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

S. Forbes, B. Harding, C. Edwards, 1998, American journal of human genetics.

Quantitative trait loci for hypercalciuria in a rat model of kidney stone disease.

Ś. Sen, R. Thakker, C. Szpirer, 2003, Journal of the American Society of Nephrology : JASN.

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

M. McCarthy, M. Sheppard, R. Thakker, 1997, Journal of medical genetics.

A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.

B. Harding, R. Thakker, S. Mumm, 2000, The Journal of clinical endocrinology and metabolism.

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

J. Carpten, E. Gillanders, J. Trent, 2002, Nature Genetics.

Multiple endocrine neoplasia type 1.

R. Thakker, A. A. Pannett, 1999, Endocrine-related cancer.

Frequent Occurrence of an Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1

S. Ellard, S. Forbes, B. Harding, 2002 .

Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis.

R. Thakker, A. A. Pannett, 2001, The Journal of clinical endocrinology and metabolism.

The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.

R. Thakker, L. Sobrinho, T. Krausz, 2001, QJM : monthly journal of the Association of Physicians.

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

S. Forbes, B. Harding, R. Trembath, 2003, Clinical endocrinology.

Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)

M. McCarthy, C. Larsson, B. Teh, 1997, Human Genetics.

Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.

A. Hattersley, S. Ellard, S. Forbes, 2002, The Journal of clinical endocrinology and metabolism.

Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).

C. Larsson, B. Teh, S. Forbes, 1996, Genomics.

Studies of the Murine Homolog of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene, men1

S. Forbes, B. Harding, P. Rashbass, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.

C. Larsson, N. Hayward, B. Teh, 1997, Human molecular genetics.

LOCALIZATION OF A TUMOR-SUPPRESSOR GENE CAUSING PARATHYROID TUMORS TO CHROMOSOME-1P34-P36

R. Thakker, C. Williamson, J. Monson, 1995 .

Multiple endocrine neoplasia type 1.

R. Thakker, A. A. Pannett, Rajesh V. Thakker, 1999, Endocrine-related cancer.