(Q37498443)

20 August 2017

Mutation analysis of mitogen activated protein kinase 1 gene in Indian cases of 46,XY disorder of sex development (English)

1 reference

20 August 2017

0 references

Dhanjit Kumar Das

1

1 reference

20 August 2017

Subodh G Rahate

2

1 reference

20 August 2017

Bhakti P Mehta

3

1 reference

20 August 2017

Harshavardhan M Gawde

4

1 reference

20 August 2017

Parag M Tamhankar

5

1 reference

20 August 2017

1 October 2013

1 reference

Indian Journal of Human Genetics

20 August 2017

1 reference

20 August 2017

19

1 reference

20 August 2017

4

1 reference

20 August 2017

437-442

1 reference

Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors.

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Minor abnormalities of testis development in mice lacking the gene encoding the MAPK signalling component, MAP3K1.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

MEKK1 binds raf-1 and the ERK2 cascade components

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Understanding the genetic aetiology in patients with XY DSD.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Novel homozygous mutations in Desert hedgehog gene in patients with 46,XY complete gonadal dysgenesis and prediction of its structural and functional implications by computational methods

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3897139

Multilocus analysis of candidate genes involved in neurogenic inflammation in pediatric asthma and related phenotypes: a case-control study

6 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24497709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Excess DAX1 Leads to XY Ovotesticular Disorder of Sex Development (DSD) in Mice by Inhibiting Steroidogenic Factor-1 (SF1) Activation of the Testis Enhancer ofSRY-box-9(Sox9)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24497709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4103/0971-6866.124372

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

24497709

1 reference