List of works by Rajesh Thakker

10 Multiple endocrine neoplasia

scientific article published on 01 November 1988

A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

scientific article published on 05 January 2016

A calcium-sensing receptor mutation causing hypocalcemia disrupts a transmembrane salt bridge to activate β-arrestin-biased signaling.

scientific article published on 20 February 2018

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

scientific article (publication date: May 1992)

A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel gene

article

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

scientific article

A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia

scientific article

A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism.

scientific article published on 12 May 2010

A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress

scientific article

A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to aCol2a1mutation

article

A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation

scientific article

A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis

scientific article

A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis

scientific article published on 28 June 2005

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1

scientific article published on 27 March 2007

Aberrant methylation underlies insulin gene expression in human insulinoma

scientific article published on 15 October 2020

Absence of mutations in the growth hormone (GH)-releasing hormone receptor gene in GH-secreting pituitary adenomas

article

Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification

scholarly article

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effects

scientific article

Allelic deletion in pituitary adenomas reflects aggressive biological activity and has potential value as a prognostic marker

scientific article published on 01 March 1997

Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders

scientific article published on 18 March 2016

Altered polarity and expression of H+-ATPase without ultrastructural changes in kidneys of Dent's disease patients

scientific article

An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess

scientific article

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

scientific article

Anatomic and functional imaging of metastatic carcinoid tumors

scientific article

Animal models of pituitary neoplasia

scientific article

Anthropometric measurements in patients with growth hormone deficiency before treatment with human growth hormone

scientific article published on 01 May 1980

Association between genotype and phenotype in uromodulin-associated kidney disease

scientific article published on 30 May 2013

Association of familial duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22

article

Association studies of calcium-sensing receptor (CaSR) polymorphisms with serum concentrations of glucose and phosphate, and vascular calcification in renal transplant recipients

scientific article

Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.

scientific article published on 21 July 2009

Author Correction: Skeletal and extraskeletal disorders of biomineralization

correction of a scholarly article

Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5

scientific article

CDC73 intragenic deletion in familial primary hyperparathyroidism associated with parathyroid carcinoma

scientific article

Calcilytic NPSP795 Increases Plasma Calcium and PTH in an Autosomal Dominant Hypocalcemia Type 1 Mouse Model

scientific article published on 07 September 2020

Calcimimetic and calcilytic therapies for inherited disorders of the calcium-sensing receptor signalling pathway

scientific article published on 11 November 2017

Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism

scientific article published on 18 May 2013

Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors.

scientific article

Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1.

scientific article published on 09 July 2015

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

scientific article

Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome

scientific article published on 21 September 2006

Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.

scientific article

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

scientific article published on 24 February 2004

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

scientific article

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations

scientific article published on April 2016

Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease

scientific article published on 01 August 2000

Clinical features of X-linked nephrolithiasis in childhood

scientific article published on 01 October 1998

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

scientific article

Clinically relevant genetic advances in endocrinology.

scientific article published in June 2013

Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

scientific article

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3.

scientific article

Confusing genes: a patient with MEN2A and Cushing's disease

scientific article published on 6 April 2013

Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.

scientific article published in November 2002

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.

scientific article

Cox-2 promotes chromogranin A expression and bioactivity: evidence for a prostaglandin E2-dependent mechanism and the involvement of a proximal cyclic adenosine 5'-monophosphate-responsive element

scientific article published on 31 May 2007

Dent's disease

scientific article

Dent's disease

scientific article published on 19 July 2005

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.

scientific article

Determination of a molecular map position for Hyp using a new interspecific backcross produced by in vitro fertilization

scientific article published on 01 November 1991

Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop.

scientific article

Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1)

scientific article published on 01 January 2010

Diseases associated with the extracellular calcium-sensing receptor

scientific article published on March 2004

Disorders of the calcium-sensing receptor

scientific article published on 01 December 1998

EagI and NotI linking clones from human chromosomes 11 and Xp.

scientific article published on June 1996

Epidemiology and Diagnosis of Hypoparathyroidism

scientific article

Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages

scientific article published on 10 May 2010

Evidence for the Role of Megalin in Renal Uptake of Transthyretin

scientific article published in Journal of Biological Chemistry

Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

scientific article published on May 1997

Expression and chromosomal localization of the Requiem gene

scientific journal article

Expression and cloning of the human X-linked hypophosphatemia gene cDNA

scientific article

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

article

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome

scientific article published on 01 July 2002

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

scientific article published on 01 June 2002

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome

scientific article published on 10 February 2005

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

scientific article published on 8 January 2007

Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral density

scientific article published on November 2006

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease

scientific article published in December 1998

GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasiveness

scientific article published on 22 February 2013

GNAS mutations in Pseudohypoparathyroidism type 1a and related disorders

scientific article

GNAS1 mutational analysis in pseudohypoparathyroidism

scientific article published on 01 October 1998

Gastroenteropancreatic neuroendocrine tumours

scientific article

Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2

scientific journal article

Gene mapping of mineral metabolic disorders

scientific article published on January 1989

Genetic Approaches to Metabolic Bone Diseases

article

Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers

scientific article published on 08 July 2009

Genetic causes of hypercalciuric nephrolithiasis

scientific article published on 30 April 2008

Genetic developments in Hypoparathyroidism

scientific article published in The Lancet

Genetic disorders of renal electrolyte transport

scientific article

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene

scientific article published on June 1996

Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13.

scientific article

Genetic variants of calcium and vitamin D metabolism in kidney stone disease

scientific article published on 15 November 2019

Genetics of endocrine and metabolic disorders: parathyroid

scientific article published on March 2004

Genetics of hypercalciuric nephrolithiasis: renal stone disease

scientific article published on 13 September 2007

Genetics of kidney stone disease

scientific article published on 12 June 2020

Genetics of neuroendocrine and carcinoid tumours

scientific article published on December 2003

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

scientific article

Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21

article

Glomerular protein sieving and implications for renal failure in Fanconi syndrome

scientific article published on 01 November 2001

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

scientific article

Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours

scientific article

Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs)

scientific article published on 3 November 2011

Guidelines for the management of thyroid cancer

article

HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.

scientific article published on 30 November 2012

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

scientific article

Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort

scientific article

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene

scientific article

Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development

scientific article published on 15 May 2012

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites.

scientific article published on 14 March 2012

Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)

scientific article published on 28 January 2016

Identification of a Second Kindred with Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Narrows Localization to a <3.5 Megabase Pair Region on Chromosome 19q13.3

scientific article published on 04 February 2010

In memoriam: Oliver M. Wrong

scientific article published in July 2012

Inherited forms of rickets and osteomalacia

scientific article published on February 1988

Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

scientific article

Investigating hypocalcaemia

scientific article published in the British Medical Journal

Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria

scientific article published on 01 January 2000

Kidney stones: a fetal origins hypothesis

scientific article published on December 2013

Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity

scientific article published on 01 August 1997

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families

scientific article published in October 1990

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

scientific article published in August 1995

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

scientific article

Localization of gastrinomas by selective intra-arterial calcium injection

scientific article published in December 2002

Lymphatic vessels are present in phosphaturic mesenchymal tumours

scientific article published on 3 August 2007

MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas

scientific article

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

scientific article

Management of Hypoparathyroidism: Summary Statement and Guidelines

scientific article published on 4 March 2016

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis

scientific article published on 01 July 1986

Mapping of the gene encoding the B56 beta 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)

scientific article (publication date: September 1997)

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

article

Membrane targeting and secretion of mutant uromodulin in familial juvenile hyperuricemic nephropathy

scientific article published on 6 December 2006

Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.

scientific article

Molecular genetic advances in pituitary tumor development

article

Molecular genetic studies of sporadic pituitary tumors

scientific article published on 01 February 1994

Molecular genetics of disorders of calcium homeostasis

scientific article

Molecular genetics of mineral metabolic disorders

scientific article published on January 1, 1992

Mouse models for inherited endocrine and metabolic disorders.

scientific article published on 15 July 2011

Multiple endocrine neoplasia type 1 (MEN1)

scientific article

Multiple endocrine neoplasia type 1 (MEN1) 5' UTR deletion, in MEN1 family, decreases menin expression

scientific article published on 11 August 2020

Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)

scientific article

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

scientific article published on 01 May 2003

Multiple endocrine neoplasia type 1 (MEN1).

scientific article published on January 1994

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

scientific article

Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia

scientific article published on 20 July 2009

Multiple endocrine neoplasia--syndromes of the twentieth century

scientific article published on 01 August 1998

Multiple endocrine neoplasia: spectrum of radiologic appearances and discussion of a multitechnique imaging approach

scientific article

Multiscale alterations in bone matrix quality increased fragility in steroid induced osteoporosis

scientific article

Mutant Prolactin Receptor and Familial Hyperprolactinemia

scientific article published on 01 March 2014

Mutant prolactin receptor and familial hyperprolactinemia

scientific article

Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda

scientific article published on 01 July 2001

Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease

scientific article

Mutational analysis of PHEX gene in X-linked hypophosphatemia

scientific article published on 01 October 1998

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

article

Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3).

scientific article published on 7 April 2014

Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia

scientific article

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.

scientific article published on 9 December 2012

N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse models

scientific article

N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.

scientific article published in May 2017

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy

scientific article published in October 2004

Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism

scientific article

OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability

scientific article (publication date: 2009)

Oncogenic hypophosphataemic osteomalacia: biomarker roles of fibroblast growth factor 23, 1,25-dihydroxyvitamin D3 and lymphatic vessel endothelial hyaluronan receptor 1.

scientific article published in February 2008

Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal.

scientific article published on 11 September 2006

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

scientific article

Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice

scientific journal article

Parafibromin--functional insights

scientific article published on July 2009

Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT) n polymorphism

article

Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1-Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progression ⬇️

scientific article published on 18 March 2016

Phase II study of single agent capecitabine in the treatment of metastatic non-pancreatic neuroendocrine tumours

scientific article

Presentation of Hypoparathyroidism: Etiologies and Clinical Features

scientific article

Prolactinoma presenting in identical twins with multiple endocrine neoplasia type 1

scientific article published on 01 July 1996

Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors

scientific article published on 28 September 2012

Pseudohypoparathyroidism type 1a due to a novel mutation in the GNAS gene

scientific article published on 24 September 2015

Quantitative Trait Loci for Hypercalciuria in a Rat Model of Kidney Stone Disease

scientific article published on 01 July 2003

Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients

scientific article published on 9 April 2013

Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

scientific article published on 01 September 1999

Role of Ca2+ and L-Phe in regulating functional cooperativity of disease-associated "toggle" calcium-sensing receptor mutations

scientific article

Role of multiple endocrine neoplasia type 1 mutational analysis in clinical practice

scientific article

SEDLIN forms homodimers: characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1.

scientific article

Sequence Analysis of 139 kb in Xp22.1 Containing Spermine Synthase and the 5′ Region of PEX ⬇️

scientific article published on September 1, 1997

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

scientific article published on April 1999

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging

scientific article

Skeletal and extraskeletal disorders of biomineralization

scientific article published in 2022

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

scientific article published on 01 September 2001

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

scientific article published on September 1989

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.

scientific article

Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone.

scientific article published on 3 November 2012

The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type 1 (ADH1).

scientific article

The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases

scientific article published on 01 December 2018

The calcium-sensing receptor: And its involvement in parathyroid pathology

scientific article published on 21 April 2015

The calcium-sensing receptor: insights into extracellular calcium homeostasis in health and disease

scientific article published on September 1997

The role of biomineralization in disorders of skeletal development and tooth formation

scientific article published in 2021

The role of renal chloride channel mutations in kidney stone disease and nephrocalcinosis

scientific article

The role of routine intravenous urography in patients with primary hyperparathyroidism

scientific article published on 01 July 1987

Transcription factors in parathyroid development: lessons from hypoparathyroid disorders

scientific article

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases

scientific article published on 01 January 2000

UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy

scientific article published in March 2003

Unravelling of the molecular mechanisms of kidney stones

scientific article published in The Lancet

Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum

scientific article published on 22 May 2009

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

scientific article published on 01 January 2005

Whole-exome sequencing studies of nonfunctioning pituitary adenomas

scientific article published on 28 February 2013

Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas

scientific article

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

scientific article

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase

scientific article published on 01 December 2004

X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene

scientific article published on 01 August 2001

miR-135b- and miR-146b-dependent silencing of calcium-sensing receptor expression in colorectal tumors.

scientific article published on 14 July 2015

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