Multiple endocrine neoplasia type 1

Por Thakker, R. V.
Publicado em 2012

Calcium-sensing receptor: Role in health and disease

Por Thakker, R. V.
Publicado em 2012

Animal models of pituitary neoplasia

Por Lines, K.E., Stevenson, M., Thakker, R.V.
Publicado no Mol Cell Endocrinol (2016)

Persistent nephrogenic diabetes insipidus, hyperparathyroidism, and hypothyroidism after lithium treatment.

Por Cairns, S R, Wolman, R, Lewis, J G, Thakker, R
Publicado em 1985

Value of routine chest radiography in an acute geriatric unit.

Por Denham, M, Thakker, R, de Lacey, G, Berman, L
Publicado em 1984

Embolisation of gastroduodenal artery aneurysm caused by chronic pancreatitis.

Por Thakker, R V, Gajjar, B, Wilkins, R A, Levi, A J
Publicado em 1983

Structure and methylation of the human calcitonin/alpha-CGRP gene.

Por Broad, P M, Symes, A J, Thakker, R V, Craig, R K
Publicado em 1989

mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Por Mumm, S, Whyte, M P, Thakker, R V, Buetow, K H, Schlessinger, D
Publicado em 1997

Utilisation of a cryptic non-canonical donor splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism

Por Bradley, K, Cavaco, B, Bowl, M, Harding, B, Young, A, Thakker, R
Publicado em 2005

Functional characterization of calcium-sensing receptor mutations expressed in human embryonic kidney cells.

Por Pearce, S H, Bai, M, Quinn, S J, Kifor, O, Brown, E M, Thakker, R V
Publicado em 1996

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

Por Lloyd, S E, Pearce, S H, Günther, W, Kawaguchi, H, Igarashi, T, Jentsch, T J, Thakker, R V
Publicado em 1997

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families.

Por Beales, P L, Warner, A M, Hitman, G A, Thakker, R, Flinter, F A
Publicado em 1997

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

Por Lloyd, S E, Pannett, A A, Dixon, P H, Whyte, M P, Thakker, R V
Publicado em 1999

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.

Por Thakker, R V, Davies, K E, Whyte, M P, Wooding, C, O'Riordan, J L
Publicado em 1990

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Por Scheinman, S J, Pook, M A, Wooding, C, Pang, J T, Frymoyer, P A, Thakker, R V
Publicado em 1993

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.

Por Thakker, R V, Pook, M A, Wooding, C, Boscaro, M, Scanarini, M, Clayton, R N
Publicado em 1993

A MEN1 pancreatic neuroendocrine tumour mouse model under temporal control

Por Lines, K E, Vas Nunes, R P, Frost, M, Yates, C J, Stevenson, M, Thakker, R V
Publicado no Endocr Connect (2017)

In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium hom...

Por Bai, M, Pearce, S H, Kifor, O, Trivedi, S, Stauffer, U G, Thakker, R V, Brown, E M, Steinmann, B
Publicado em 1997

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Por Trump, D, Dixon, P H, Mumm, S, Wooding, C, Davies, K E, Schlessinger, D, Whyte, M P, Thakker, R V
Publicado em 1998

Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours

Por Farrell, W E, Simpson, D J, Bicknell, J, Magnay, J L, Kyrodimou, E, Thakker, R V, Clayton, R N
Publicado em 1999