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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and PROK2[original query]
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
The Journal of clinical endocrinology and metabolism 2008 Oct 93 (10): 4113-8.
Abreu Ana Paula, Trarbach Ericka Barbosa, de Castro Margaret, Frade Costa Elaine Maria, Versiani Beatriz, Matias Baptista Maria Tereza, Garmes Heraldo Mendes, Mendonca Berenice Bilharinho, Latronico Ana Claud
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Dec 169 (6): 805-9.
Sarfati Julie, Fouveaut Corinne, Leroy Chrystel, Jeanpierre Marc, Hardelin Jean-Pierre, Dodé Catheri
Huntington's disease biomarker progression profile identified by transcriptome sequencing in peripheral blood.
European journal of human genetics : EJHG 2015 Oct 23 (10): 1349-56.
Mastrokolias Anastasios, Ariyurek Yavuz, Goeman Jelle J, van Duijn Erik, Roos Raymund Ac, van der Mast Roos C, van Ommen GertJan B, den Dunnen Johan T, 't Hoen Peter Ac, van Roon-Mom Willeke
Differences in the Platelet mRNA Landscape Portend Racial Disparities in Platelet Function and Suggest Novel Therapeutic Targets.
Clinical pharmacology and therapeutics 2021 7 110 (3): 702-713.
Garofano Kaitlin, Park C Sehwan, Alarcon Cristina, Avitia Juan, Barbour April, Diemert David, Fraser Claire M, Friedman Paula N, Horvath Anelia, Rashid Kameron, Shaazuddin Mohammed, Sidahmed Alfateh, O'Brien Travis J, Perera Minoli A, Lee Norman
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