Results 291 to 300 of about 62,177 (350)

Long-term seed aid in Ethiopia: past, present, and future perspectives [PDF]

, 2007
Assefa, S., Assefa, T., Deressa, A., Mcguire, S., Sperling, L.   +4 more
core  

Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study.

J Clin Endocrinol Metab
Naamneh Elzenaty R, Martinez de Lapiscina I, Kouri C, Sauter KS, Sommer G, Castaño L, Flück CE.   +6 more
europepmc   +1 more source

Distributed blockchain assisted secure data aggregation scheme for risk-aware zone-based MANET. [PDF]

Sci Rep
Sugumaran VR, Dinesh E, Ramya R, Muniyandy E.   +3 more
europepmc   +1 more source

46, XY Complete Gonadal Dysgenesis (Swyer Syndrome) Presenting as Primary Amenorrhea in a Normomorphic Adult Female From Kakamega, Kenya. [PDF]

Clin Case Rep
Omoaghe C.
europepmc   +1 more source

Impact of COVID-19 on the HIV Treatment Outcomes Among Men Who Have Sex with Men in South Africa After the Implementation of a Differentiated Service Delivery Model: An Interrupted Time Series Analysis. [PDF]

Int J Environ Res Public Health
Sebati B, Phalane E, Shiferaw YA, Pienaar J, Furamera S, Phaswana-Mafuya RN.   +5 more
europepmc   +1 more source

Impacts of CACNB4 overexpression on dendritic spine density in both sexes and relevance to schizophrenia. [PDF]

Transl Psychiatry
Parker EM, Kindja NL, DeGiosio RA, Salisbury RB, Krivinko JM, Cheetham CEJ, MacDonald ML, Fan W, Cheng B, Sweet RA.   +9 more
europepmc   +1 more source

Evolution of cellular architecture and function of the hippocampus: insights from the artificial selection experiment. [PDF]

Biol Lett
Goncerzewicz A, Bonda-Ostaszewska E, Lipiec M, Knapska E, Konarzewski M.   +4 more
europepmc   +1 more source

A novel CUL4B gene variant activating Wnt4/β-catenin signal pathway to karyotype 46, XY female with disorders of sex development. [PDF]

Biol Res
Wang C, Chen H, Chen Q, Qu Y, Yuan K, Liang L, Yan Q.   +6 more
europepmc   +1 more source

Ambiguous Genitalia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency: Clinical, Genetic, and Functional Characterization of Two Novel HSD3B2 Variants. [PDF]

JCEM Case Rep
Liimatta J, Sauter K, du Toit T, Schaller A, l'Allemand D, Flück CE.   +5 more
europepmc   +1 more source

Editorial: 46,XX differences of sex development (DSD) outside congenital adrenal hyperplasia (CAH). [PDF]

Front Endocrinol (Lausanne)
Balsamo A, Bashamboo A, Bertelloni S, Lauber-Biason A.   +3 more
europepmc   +1 more source