Jose W. Saldanha

Mill Hill
London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Ultra-high resolution X-ray structures of two forms of human recombinant insulin at 100 K.

Ultra-high resolution X-ray structures of two forms of human recombinant insulin at 100 K.

Journal: Chemistry Central journal

Published: March 05, 2017

Cmr is a redox-responsive regulator of DosR that contributes to M. tuberculosis virulence.

Cmr is a redox-responsive regulator of DosR that contributes to M. tuberculosis virulence.

Journal: Nucleic acids research

Published: September 12, 2016

Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.

Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 09, 2016

TRNT1 deficiency: clinical, biochemical and molecular genetic features.

TRNT1 deficiency: clinical, biochemical and molecular genetic features.

Journal: Orphanet journal of rare diseases

Published: March 09, 2016

The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly.

The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly.

Journal: Developmental biology

Published: August 20, 2015

Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD).

Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD).

Journal: Molecular and cellular endocrinology

Published: March 21, 2015

Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation.

Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation.

Journal: Journal of inherited metabolic disease

Published: November 23, 2014

The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism.

The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism.

Journal: Clinical endocrinology

Published: July 23, 2014

Disjoint combinations profiling (DCP): a new method for the prediction of antibody CDR conformation from sequence.

Disjoint combinations profiling (DCP): a new method for the prediction of antibody CDR conformation from sequence.

Journal: PeerJ

Published: March 26, 2014

A complete, multi-level conformational clustering of antibody complementarity-determining regions.

A complete, multi-level conformational clustering of antibody complementarity-determining regions.

Journal: PeerJ

Published: March 23, 2014

FAN1 activity on asymmetric repair intermediates is mediated by an atypical monomeric virus-type replication-repair nuclease domain.

FAN1 activity on asymmetric repair intermediates is mediated by an atypical monomeric virus-type replication-repair nuclease domain.

Journal: Cell reports

Published: February 07, 2014

Crystal structure reveals conservation of amyloid-β conformation recognized by 3D6 following humanization to bapineuzumab.

Crystal structure reveals conservation of amyloid-β conformation recognized by 3D6 following humanization to bapineuzumab.

Journal: Alzheimer's research & therapy

Published: January 24, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026