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Muhammad Wajid Selected Research

Hypotrichosis

8/2009Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis.
3/2009Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis.
1/2009The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis.
2/2008P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle.
7/2007Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family.

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Muhammad Wajid Research Topics

Disease

5Hypotrichosis
08/2009 - 07/2007
2Parkinson Disease (Parkinson's Disease)
01/2021 - 01/2021
2Dyslipidemias (Dyslipidemia)
03/2019 - 11/2016
2type 2 Syndactyly
10/2011 - 12/2007
2Palmoplantar Keratoderma (Keratosis Palmaris et Plantaris)
03/2009 - 03/2007
1Typhoid Fever (Typhoid)
08/2022
1Sleep Wake Disorders
01/2022
1Synucleinopathies
01/2021
1Alzheimer Disease (Alzheimer's Disease)
01/2021
1Cardiovascular Diseases (Cardiovascular Disease)
01/2021
1Neoplasms (Cancer)
01/2021
1Mitochondrial Diseases (Mitochondrial Disease)
01/2021
1Chronic Obstructive Pulmonary Disease (COPD)
01/2021
1Hyperglycemia
03/2019
1Insulin Resistance
03/2019
1Neurodegenerative Diseases (Neurodegenerative Disease)
01/2019
1Snake Bites (Snake Bite)
11/2016
1Bites and Stings (Sting)
11/2016
1Ectodermal Dysplasia (Aplasia Cutis Congenita)
03/2010
1Congenital Pain Insensitivity
01/2010
1Anodontia (Hypodontia)
12/2009
1Alopecia (Baldness)
04/2008
1Atrichia with Papular Lesions
04/2008
1Cysts
04/2008
1Retinoblastoma (Glioblastoma, Retinal)
03/2008
1Ectodermal dysplasia, ectrodactyly, and macular dystrophy
02/2008
1Macular Degeneration (Age-Related Maculopathy)
02/2008
1Epidermolysis Bullosa Dystrophica (Dystrophic Epidermolysis Bullosa)
11/2006
1Skin Diseases (Skin Disease)
11/2006
1Anonychia congenita
11/2006
1Hearing Loss (Hearing Impairment)
10/2003

Drug/Important Bio-Agent (IBA)

3Nonsense Codon (Nonsense Mutation)IBA
10/2011 - 12/2009
3Lipase (Acid Lipase)FDA Link
08/2009 - 01/2009
2Insulin (Novolin)FDA Link
01/2021 - 03/2019
2CholesterolIBA
03/2019 - 11/2016
2oxidized low density lipoproteinIBA
03/2019 - 11/2016
2AlloxanIBA
03/2019 - 11/2016
2Triglycerides (Triacylglycerol)IBA
03/2019 - 11/2016
2FructoseIBA
03/2019 - 11/2016
2Keratins (Keratin)IBA
03/2010 - 04/2008
2Desmoglein 1IBA
03/2009 - 03/2007
1Pharmaceutical PreparationsIBA
08/2022
1Uric Acid (Urate)IBA
01/2022
1Blood Glucose (Blood Sugar)IBA
01/2022
1Glucosylceramidase (Glucocerebrosidase)IBA
01/2021
1Adiponectin ReceptorsIBA
01/2021
1Hypoglycemic Agents (Hypoglycemics)IBA
03/2019
1RNA (Ribonucleic Acid)IBA
01/2019
1LaxativesIBA
11/2016
1DiureticsIBA
11/2016
1G-Protein-Coupled Receptors (Receptors, G Protein Coupled)IBA
03/2008
1Cadherins (E-Cadherin)IBA
02/2008
1polyalanineIBA
12/2007
1Alanine (L-Alanine)FDA Link
12/2007
1DesmogleinsIBA
07/2007
1Proteins (Proteins, Gene)FDA Link
11/2006
1Glycine (Aminoacetic Acid)FDA LinkGeneric
11/2006
1Collagen Type VIIIBA
11/2006

Therapy/Procedure

1Therapeutics
01/2021
1Sign Language
10/2003